RefSeQID Symbol PUBMEDID Link Disease/Trait SNPs p-Value Study Database
NM_000015 NAT2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4646249 7.28E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_000015 NAT2 21572414 http://www.ncbi.nlm.nih.gov/pubmed/21572414 Metabolism rs4921914 1.00E-28 A genome-wide association study of metabolic traits in human urine. NHGRI|-1
NM_000015 NAT2 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs1495741 4.00E-11 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_000016 ACADM 20037589 http://www.ncbi.nlm.nih.gov/pubmed/20037589 Nonalcoholic Fatty Liver Disease rs211718 1.00E-63 A genome-wide perspective of genetic variation in human metabolism. NHGRI|-1
NM_000017 ACADS 20037589 http://www.ncbi.nlm.nih.gov/pubmed/20037589 Nonalcoholic Fatty Liver Disease rs2014355 5.00E-96 A genome-wide perspective of genetic variation in human metabolism. NHGRI|-1
NM_000027 AGA 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11947216 3.31E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_000027 AGA 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10031053 1.54E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_000027 AGA 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs9993819 5.49E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_000027 AGA 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs569945 8.85E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_000027 AGA 17903306 http://www.ncbi.nlm.nih.gov/pubmed/17903306 Heart Rate rs1395479 7.00E-06 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. NHGRI|-1
NM_000028 AGL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs17121644 4.78E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000033 ABCD1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11156606 3.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_000037 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs6474359 1.00E-08 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_000037 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs4737009 6.00E-12 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_000037 ANK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4466386 6.52E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_000041 APOE 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs769449 9.00E-21 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_000041 APOE 21123754 http://www.ncbi.nlm.nih.gov/pubmed/21123754 Alzheimer Disease rs429358 1.00E-06 "Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort." NHGRI|-1
NM_000041 APOE 21123754 http://www.ncbi.nlm.nih.gov/pubmed/21123754 Alzheimer Disease rs439401 1.00E-06 "Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort." NHGRI|-1
NM_000041 APOE 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs439401 1.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000041 APOE 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Triglycerides rs439401 2.00E-09 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000041 APOE 20838585 http://www.ncbi.nlm.nih.gov/pubmed/20838585 Cardiovascular Diseases rs445925 9.00E-19 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. NHGRI|-1
NM_000043 FAS 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs2234978 6.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_000043 FAS 21041692 http://www.ncbi.nlm.nih.gov/pubmed/21041692 Heart Function Tests rs1937332 7.00E-07 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. NHGRI|-1
NM_000043 FAS 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs11203032 8.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_000044 AR 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs5031002 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_000044 AR 18849991 http://www.ncbi.nlm.nih.gov/pubmed/18849991 Alopecia rs6625163 5.00E-11 Male-pattern baldness susceptibility locus at 20p11. NHGRI|-1
NM_000045 ARG1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs2807278 3.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_000046 ARSB 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs337847 7.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_000046 ARSB 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs2052550 8.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_000055 BCHE 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs1523288 6.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4437429 1.00E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4437429 4.34E-06 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9448894 7.14E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9448894 7.28E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4706113 7.14E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4706113 7.28E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2322631 4.13E-06 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2322631 9.67E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10080237 4.13E-06 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10080237 9.67E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs978814 1.91E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs978814 3.03E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3812121 2.07E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3812121 4.03E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2179842 2.61E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2179842 3.51E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9352817 8.23E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9352817 8.91E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7453746 7.12E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_000056 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7453746 7.86E-06 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000060 BTD 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs7651039 2.00E-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_000063 C2 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs9332739 2.00E-23 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1042663 2.97E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1042663 3.14E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000063 C2 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs9380272 2.00E-08 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs550605 4.38E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs550605 4.98E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs638383 4.76E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs497239 6.02E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs497239 7.82E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs547154 2.70E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs547154 2.90E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000063 C2 21105107 http://www.ncbi.nlm.nih.gov/pubmed/21105107 "Carcinoma, Hepatocellular" rs9267673 2.00E-06 Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma. NHGRI|-1
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9267673 2.30E-33 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_000063 C2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs644045 2.06E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs511294 1.45E-13 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs511294 6.27E-13 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs544167 2.48E-13 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs544167 7.79E-13 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000064 C3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs432001 1.40E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000064 C3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs432001 3.46E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000064 C3 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs2230199 1.00E-10 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_000064 C3 20861866 http://www.ncbi.nlm.nih.gov/pubmed/20861866 Macular Degeneration rs2230199 1.00E-08 Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. NHGRI|-1
NM_000064 C3 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs2230199 2.00E-08 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_000064 C3 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs2230199 5.00E-29 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_000064 C3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2250656 1.26E-07 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000064 C3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2250656 3.89E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000064 C3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs171094 1.39E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000071 CBS 20031578 http://www.ncbi.nlm.nih.gov/pubmed/20031578 Homocysteine rs6586282 3.00E-10 "Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study." NHGRI|-1
NM_000072 CD36 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs10499859 3.00E-06 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NM_000076 CDKN1C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2078786 9.55E-06 NBL-GWAS version 2 dbGaP|2895
NM_000078 CETP 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 Apolipoprotein A-I rs1800775 3.00E-06 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_000078 CETP 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, HDL" rs1800775 1.00E-73 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_000078 CETP 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Cholesterol, HDL" rs1800775 3.00E-13 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_000078 CETP 20031564 http://www.ncbi.nlm.nih.gov/pubmed/20031564 "Cholesterol, HDL" rs1800775 4.00E-93 "Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study." NHGRI|-1
NM_000078 CETP 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs1864163 7.00E-39 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_000078 CETP 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs9939224 7.00E-12 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000078 CETP 20066028 http://www.ncbi.nlm.nih.gov/pubmed/20066028 "Cholesterol, HDL" rs1532624 3.00E-20 Modeling of environmental effects in genome-wide association studies identifies SLC2A2 and HP as novel loci influencing serum cholesterol levels. NHGRI|-1
NM_000078 CETP 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, HDL" rs1532624 9.00E-94 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000078 CETP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs1532624 2.97E-22 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_000078 CETP 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 "Cholesterol, HDL" rs7499892 9.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_000078 CETP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs7499892 2.29E-16 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_000078 CETP 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs9989419 3.00E-31 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_000078 CETP 20031538 http://www.ncbi.nlm.nih.gov/pubmed/20031538 "Cholesterol, HDL" rs9989419 9.00E-27 Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions. NHGRI|-1
NM_000078 CETP 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs9989419 1.00E-32 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_000078 CETP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs9989419 2.21E-09 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_000078 CETP 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs173539 4.00E-75 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000078 CETP 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs173539 5.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000078 CETP 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs173539 1.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000078 CETP 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs173539 9.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000078 CETP 20838585 http://www.ncbi.nlm.nih.gov/pubmed/20838585 Cardiovascular Diseases rs247616 1.00E-23 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. NHGRI|-1
NM_000078 CETP 18454146 http://www.ncbi.nlm.nih.gov/pubmed/18454146 "Cholesterol, HDL" rs3764261 1.00E-27 Common genetic variation near MC4R is associated with waist circumference and insulin resistance. NHGRI|-1
NM_000078 CETP 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs3764261 1.00E-48 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_000078 CETP 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs3764261 2.00E-57 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_000078 CETP 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, HDL" rs3764261 7.00E-29 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_000078 CETP 19359809 http://www.ncbi.nlm.nih.gov/pubmed/19359809 "Cholesterol, LDL" rs3764261 3.00E-12 Identification of genetic markers associated with high-density lipoprotein-cholesterol by genome-wide screening in a Japanese population: the Suita study. NHGRI|-1
NM_000078 CETP 20686565 http://www.ncbi.nlm.nih.gov/pubmed/20686565 Lipids rs3764261 7E-380 "Biological, clinical and population relevance of 95 loci for blood lipids." NHGRI|-1
NM_000078 CETP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs3764261 6.97E-29 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_000078 CETP 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs3764261 7.00E-07 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_000078 CETP 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs3764261 7.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_000078 CETP 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs3764261 3.00E-13 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000084 CLCN5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1553510 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_000086 CLN3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs151181 2.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_000088 COL1A1 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs2075555 8.00E-08 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_000089 COL1A2 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Vital Capacity rs441051 2.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_000093 COL5A1 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs7044529 5.00E-08 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_000093 COL5A1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs7874142 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_000098 CPT2 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs6695567 4.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_000098 CPT2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1288331 3.44E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_000099 CST3 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs911119 2.00E-138 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_000102 CYP17A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17115100 2.46E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_000102 CYP17A1 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs17115100 7.00E-08 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_000102 CYP17A1 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs1004467 1.00E-10 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_000103 CYP19A1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs2305707 7.00E-07 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_000104 CYP1B1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1800440 1.30E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_000108 DLD 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 "Colitis, Ulcerative" rs2108225 1.00E-07 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_000108 DLD 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs4730273 5.00E-06 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_000108 DLD 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs4730276 9.00E-06 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_000108 DLD 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs4510766 2.00E-16 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_000108 DLD 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs886774 3.00E-08 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_000108 DLD 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs4598195 1.00E-06 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_000108 DLD 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs4598195 8.00E-08 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_000109 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_000109 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_000110 DPYD 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs11165846 9.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_000111 SLC26A3 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 "Colitis, Ulcerative" rs2108225 1.00E-07 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_000111 SLC26A3 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs4730273 5.00E-06 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_000111 SLC26A3 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs4730276 9.00E-06 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_000111 SLC26A3 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs4510766 2.00E-16 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_000111 SLC26A3 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs886774 3.00E-08 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_000111 SLC26A3 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs4598195 1.00E-06 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_000111 SLC26A3 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs4598195 8.00E-08 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_000115 EDNRB 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs9574199 7.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_000115 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6563036 6.86E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_000115 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7996252 2.72E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_000115 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7996252 8.44E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_000115 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2248525 3.14E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_000115 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2248525 8.12E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_000115 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2265775 5.77E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_000115 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2987526 3.23E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_000118 ENG 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Blood Pressure rs7865146 1.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_000125 ESR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2941740 2.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_000125 ESR1 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs1999805 2.00E-08 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_000125 ESR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2504063 6.00E-11 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_000125 ESR1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs543650 1.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_000125 ESR1 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs6902771 8.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_000125 ESR1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs2982694 7.00E-10 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_000125 ESR1 19219042 http://www.ncbi.nlm.nih.gov/pubmed/19219042 Breast Neoplasms rs2046210 2.00E-15 Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. NHGRI|-1
NM_000127 EXT1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs11989122 6.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_000127 EXT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs11562721 9.19E-05 NBL-GWAS version 2 dbGaP|2895
NM_000127 EXT1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs723268 8.86E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_000127 EXT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs3105764 5.46E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_000129 F13A1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs749005 3.00E-07 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_000130 F5 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs6687813 2.00E-14 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_000131 F7 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Factor VII rs561241 5.00E-16 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_000134 FABP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1546505 8.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_000134 FABP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10213554 1.16E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_000135 FANCA 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12931267 3.00E-10 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_000135 FANCA 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12931267 5.00E-87 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_000135 FANCA 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Melanosis rs12931267 8.00E-62 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_000135 FANCA 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs16966142 6.00E-06 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_000137 FAH 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs11634397 2.00E-09 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_000138 FBN1 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs1876206 6.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_000138 FBN1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs17463995 4.89E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_000141 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11200014 9.14E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_000141 FGFR2 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs2981579 2.00E-10 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_000141 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2981579 4.36E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_000141 FGFR2 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2981579 4.00E-31 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_000141 FGFR2 21060860 http://www.ncbi.nlm.nih.gov/pubmed/21060860 Breast Neoplasms rs2981575 1.00E-08 Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. NHGRI|-1
NM_000141 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1219648 1.34E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_000141 FGFR2 17529973 http://www.ncbi.nlm.nih.gov/pubmed/17529973 Breast Neoplasms rs1219648 1.00E-10 A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. NHGRI|-1
NM_000141 FGFR2 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs1219648 1.00E-30 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_000141 FGFR2 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs1219648 2.00E-13 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_000141 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2420946 1.74E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_000141 FGFR2 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs2981582 2.00E-76 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_000141 FGFR2 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs2901286 4.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_000141 FGFR2 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs10788160 5.00E-15 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_000145 FSHR 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs2268363 5.00E-08 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_000145 FSHR 19165918 http://www.ncbi.nlm.nih.gov/pubmed/19165918 "Lupus Erythematosus, Systemic" rs17039212 9.00E-06 Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. NHGRI|-1
NM_000145 FSHR 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs7591064 5.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_000153 GALC 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs11624056 3.00E-08 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_000153 GALC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1385397 5.84E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_000153 GALC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2401711 9.82E-05 NBL-GWAS version 2 dbGaP|2895
NM_000153 GALC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7152233 7.28E-06 NBL-GWAS version 2 dbGaP|2895
NM_000158 GBE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9849596 1.50E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000158 GBE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9309828 3.79E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000158 GBE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2055451 2.72E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_000158 GBE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2055451 2.98E-07 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_000158 GBE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1502305 1.98E-06 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_000158 GBE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1502304 2.36E-06 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_000158 GBE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7641536 4.04E-05 NBL-GWAS version 2 dbGaP|2895
NM_000158 GBE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2340388 2.82E-05 NBL-GWAS version 2 dbGaP|2895
NM_000158 GBE1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2340388 8.03E-06 NBL-GWAS version 1 dbGaP|2845
NM_000158 GBE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs949455 7.12E-05 NBL-GWAS version 2 dbGaP|2895
NM_000159 GCDH 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs11085824 1.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_000162 GCK 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs730497 6.00E-12 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_000162 GCK 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1799884 1.00E-20 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_000162 GCK 19060907 http://www.ncbi.nlm.nih.gov/pubmed/19060907 Blood Glucose rs4607517 1.00E-25 Variants in MTNR1B influence fasting glucose levels. NHGRI|-1
NM_000162 GCK 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4607517 7.00E-92 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_000162 GCK 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs4607517 2.00E-16 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_000163 GHR 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs13188386 8.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_000163 GHR 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs979233 4.00E-06 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_000164 GIPR 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs10423928 3.00E-12 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_000165 GJA1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 gamma-Glutamyltransferase rs4541776 2.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_000165 GJA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9490327 2.09E-06 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_000165 GJA1 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs11154022 7.00E-08 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_000173 GP1BA 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Platelet Count rs6065 2.00E-12 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_000179 MSH6 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs77155169 2.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs505102 1.07E-40 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs505102 9.09E-46 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs800292 1.68E-07 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs800292 2.21E-47 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs800292 5.05E-11 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs800292 9.78E-42 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000186 CFH 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs1329424 6.00E-16 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs572515 1.22E-15 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs572515 4.10E-21 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3766404 2.44E-21 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3766404 2.50E-23 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7529589 1.60E-14 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7529589 2.67E-19 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_000186 CFH 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs1061170 1.00E-261 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_000186 CFH 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs1061170 4.00E-117 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801555 1.33E-71 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801555 3.74E-84 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10754199 1.17E-85 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10754199 7.71E-73 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12038333 2.77E-20 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12038333 4.47E-15 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2019727 2.99E-12 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2019724 2.07E-88 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2019724 9.52E-75 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000186 CFH 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs10737680 2.00E-76 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs203674 1.29E-25 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs203674 6.04E-18 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_000186 CFH 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 "Glomerulonephritis, IGA" rs6677604 3.00E-10 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6677604 1.65E-32 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6677604 9.46E-38 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs419137 1.06E-10 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs419137 2.33E-09 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000186 CFH 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs1410996 2.00E-111 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs380390 1.75E-19 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs380390 4.00E-08 Complement factor H polymorphism in age-related macular degeneration. NHGRI|-1
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2284664 2.28E-36 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2284664 2.81E-41 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1329428 1.35E-16 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_000186 CFH 20861866 http://www.ncbi.nlm.nih.gov/pubmed/20861866 Macular Degeneration rs1329428 3.00E-64 Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. NHGRI|-1
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1329428 6.93E-76 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000186 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1329428 8.92E-92 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000188 HK1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs16926246 2.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_000188 HK1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs16926246 1.00E-13 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_000188 HK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs16926246 3.00E-54 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_000188 HK1 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs7072268 2.00E-25 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_000192 TBX5 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs883079 1.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_000192 TBX5 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3825214 1.00E-07 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_000192 TBX5 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3825214 3.00E-12 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_000192 TBX5 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3825214 3.00E-13 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_000192 TBX5 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1946295 7.87E-06 NBL-GWAS version 1 dbGaP|2845
NM_000193 SHH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs172310 2.98E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_000193 SHH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs172310 3.95E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_000193 SHH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs167020 2.87E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_000193 SHH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs167020 7.52E-06 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_000193 SHH 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs6943029 8.00E-08 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_000193 SHH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10949808 1.72E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_000193 SHH 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs10949808 1.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_000201 ICAM1 21533024 http://www.ncbi.nlm.nih.gov/pubmed/21533024 Intercellular Adhesion Molecule-1 rs1799969 1.00E-120 "Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci." NHGRI|-1
NM_000201 ICAM1 18604267 http://www.ncbi.nlm.nih.gov/pubmed/18604267 Intercellular Adhesion Molecule-1 rs1799969 4.00E-47 "Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women." NHGRI|-1
NM_000201 ICAM1 18604267 http://www.ncbi.nlm.nih.gov/pubmed/18604267 Intercellular Adhesion Molecule-1 rs5498 5.00E-25 "Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women." NHGRI|-1
NM_000201 ICAM1 21533024 http://www.ncbi.nlm.nih.gov/pubmed/21533024 Intercellular Adhesion Molecule-1 rs5498 6.00E-89 "Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci." NHGRI|-1
NM_000201 ICAM1 18604267 http://www.ncbi.nlm.nih.gov/pubmed/18604267 Intercellular Adhesion Molecule-1 rs281437 3.00E-10 "Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women." NHGRI|-1
NM_000201 ICAM1 20167578 http://www.ncbi.nlm.nih.gov/pubmed/20167578 Intercellular Adhesion Molecule-1 rs3093030 4.00E-23 Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. NHGRI|-1
NM_000204 CFI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7439493 1.26E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000204 CFI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7439493 1.59E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000204 CFI 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs10033900 4.00E-10 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_000204 CFI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10033900 6.35E-07 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_000204 CFI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10033900 6.70E-07 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000204 CFI 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs10033900 9.00E-09 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_000208 INSR 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs2115386 3.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_000209 PDX1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs9512900 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_000210 ITGA6 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs12621278 9.00E-23 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_000214 JAG1 20096396 http://www.ncbi.nlm.nih.gov/pubmed/20096396 Bone Density rs2273061 5.00E-08 Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies. NHGRI|-1
NM_000214 JAG1 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs1884136 9.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_000217 KCNA1 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs12302829 8.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_000218 KCNQ1 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs2074238 3.00E-17 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_000218 KCNQ1 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs12296050 3.00E-17 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_000218 KCNQ1 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs12296050 8.00E-11 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_000218 KCNQ1 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12576239 1.00E-15 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_000218 KCNQ1 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs179429 7.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_000218 KCNQ1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs231362 3.00E-13 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_000218 KCNQ1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 L-Lactate Dehydrogenase rs2237878 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_000218 KCNQ1 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs2237892 1.00E-26 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_000218 KCNQ1 18711367 http://www.ncbi.nlm.nih.gov/pubmed/18711367 "Diabetes Mellitus, Type 2" rs2237892 2.00E-42 Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus. NHGRI|-1
NM_000218 KCNQ1 21573907 http://www.ncbi.nlm.nih.gov/pubmed/21573907 "Diabetes Mellitus, Type 2" rs2237892 4.00E-06 "Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas." NHGRI|-1
NM_000218 KCNQ1 20174558 http://www.ncbi.nlm.nih.gov/pubmed/20174558 "Diabetes Mellitus, Type 2" rs2237895 1.00E-09 A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. NHGRI|-1
NM_000218 KCNQ1 18711366 http://www.ncbi.nlm.nih.gov/pubmed/18711366 "Diabetes Mellitus, Type 2" rs2237897 1.00E-16 SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations. NHGRI|-1
NM_000219 KCNE1 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs727957 2.00E-12 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_000220 KCNJ1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs588407 3.45E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_000222 KIT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11732323 5.78E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_000222 KIT 18193045 http://www.ncbi.nlm.nih.gov/pubmed/18193045 Body Height rs17690232 4.00E-07 Common variants in the GDF5-UQCC region are associated with variation in human height. NHGRI|-1
NM_000222 KIT 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Count rs218237 2.00E-17 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_000222 KIT 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs218237 3.00E-25 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_000222 KIT 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs172629 1.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_000222 KIT 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs2537859 4.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_000230 LEP 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4731416 6.23E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_000231 SGCG 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs3794370 7.72E-06 NBL-GWAS version 1 dbGaP|2845
NM_000231 SGCG 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs4770394 9.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_000231 SGCG 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs9507041 8.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_000233 LHCGR 21151128 http://www.ncbi.nlm.nih.gov/pubmed/21151128 Polycystic Ovary Syndrome rs13405728 8.00E-21 "Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3." NHGRI|-1
NM_000233 LHCGR 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs7591064 5.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_000235 LIPA 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs1412444 3.00E-13 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_000235 LIPA 21606135 http://www.ncbi.nlm.nih.gov/pubmed/21606135 Coronary Artery Disease rs1412444 4.00E-08 A Genome-wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease. NHGRI|-1
NM_000236 LIPC 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, HDL" rs1800588 2.00E-32 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_000236 LIPC 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs261334 5.00E-22 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_000236 LIPC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs261336 2.51E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000236 LIPC 18084291 http://www.ncbi.nlm.nih.gov/pubmed/18084291 Amyotrophic Lateral Sclerosis rs3825776 9.00E-06 Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis. NHGRI|-1
NM_000236 LIPC 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs4775041 3.00E-20 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_000236 LIPC 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Phosphatidylethanolamines rs4775041 1.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_000236 LIPC 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs4775041 2.00E-08 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_000236 LIPC 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs10468017 8.00E-23 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000236 LIPC 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs10468017 1.00E-08 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_000236 LIPC 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs10468017 3.00E-12 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_000236 LIPC 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs10468017 6.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000236 LIPC 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2043085 1.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000236 LIPC 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, HDL" rs1532085 1.00E-35 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000236 LIPC 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, HDL" rs1532085 2.00E-10 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_000236 LIPC 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs1532085 4.00E-07 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000236 LIPC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs1532085 1.77E-10 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_000236 LIPC 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs493258 1.00E-07 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_000236 LIPC 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs493258 2.00E-08 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_000237 LPL 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs295 2.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000237 LPL 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs301 3.00E-11 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000237 LPL 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs325 8.00E-26 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_000237 LPL 18193046 http://www.ncbi.nlm.nih.gov/pubmed/18193046 Triglycerides rs326 5.00E-12 Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. NHGRI|-1
NM_000237 LPL 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, HDL" rs328 9.00E-23 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_000237 LPL 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs328 2.00E-28 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_000237 LPL 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 Triglycerides rs328 5.00E-07 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_000237 LPL 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs13702 1.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000237 LPL 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs15285 1.00E-10 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000237 LPL 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2197089 2.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000237 LPL 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs10105606 4.00E-26 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_000237 LPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs10096633 2.25E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_000237 LPL 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Triglycerides rs10096633 2.00E-18 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000237 LPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10096633 5.16E-08 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_000237 LPL 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Triglycerides rs10096633 5.00E-08 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_000237 LPL 20031538 http://www.ncbi.nlm.nih.gov/pubmed/20031538 "Cholesterol, HDL" rs17482753 3.00E-11 Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions. NHGRI|-1
NM_000237 LPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7825274 2.62E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_000237 LPL 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs12678919 2.00E-34 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000237 LPL 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs12678919 2.00E-41 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000237 LPL 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs10503669 4.00E-19 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_000237 LPL 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs10503669 4.00E-22 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_000237 LPL 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs2083637 2.00E-10 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_000237 LPL 18454146 http://www.ncbi.nlm.nih.gov/pubmed/18454146 "Cholesterol, HDL" rs2083637 5.00E-06 Common genetic variation near MC4R is associated with waist circumference and insulin resistance. NHGRI|-1
NM_000237 LPL 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, HDL" rs2083637 6.00E-18 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000237 LPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs2083637 6.53E-05 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_000237 LPL 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs1441756 3.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_000237 LPL 20657596 http://www.ncbi.nlm.nih.gov/pubmed/20657596 Hypertriglyceridemia rs7016880 2.00E-07 Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. NHGRI|-1
NM_000237 LPL 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs7816032 2.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_000238 KCNH2 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3807375 5.00E-11 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_000238 KCNH2 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs2968864 8.00E-16 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_000238 KCNH2 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs2968863 2.00E-15 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_000238 KCNH2 20062061 http://www.ncbi.nlm.nih.gov/pubmed/20062061 Electrocardiography rs4725982 3.00E-06 Genetic variation in SCN10A influences cardiac conduction. NHGRI|-1
NM_000238 KCNH2 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs4725982 5.00E-16 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_000240 MAOA 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs3027409 7.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_000242 MBL2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12412945 5.50E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_000242 MBL2 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs583012 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_000242 MBL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1932011 8.49E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000242 MBL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9416295 9.93E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000242 MBL2 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs1733724 7.00E-08 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_000242 MBL2 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs1733724 3.00E-08 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_000245 MET 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs10243024 6.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_000246 CIITA 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs4781011 3.00E-06 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_000248 MITF 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs922948 2.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_000253 MTTP 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs11735070 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_000264 PTCH1 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs16909898 5.00E-07 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_000264 PTCH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs10512248 4.00E-11 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_000264 PTCH1 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs10988802 4.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NM_000266 NDP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2238973 6.88E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_000271 NPC1 19151714 http://www.ncbi.nlm.nih.gov/pubmed/19151714 Obesity rs1805081 3.00E-07 Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. NHGRI|-1
NM_000275 OCA2 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs4778138 2.00E-24 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_000275 OCA2 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs4778138 6.00E-20 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_000275 OCA2 19772629 http://www.ncbi.nlm.nih.gov/pubmed/19772629 Parkinson Disease rs17565841 3.00E-06 Genomewide association study for onset age in Parkinson disease. NHGRI|-1
NM_000277 PAH 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs2172873 2.00E-06 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_000278 PAX2 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs4509693 6.00E-06 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_000281 PCBD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10999637 7.46E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_000281 PCBD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4746077 3.35E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_000281 PCBD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4456181 6.13E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_000281 PCBD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4456181 7.32E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_000282 PCCA 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs681561 9.81E-07 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_000284 PDHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs5955711 9.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_000288 PEX7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9373174 1.22E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_000288 PEX7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1474987 9.20E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_000288 PEX7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs6919857 9.21E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_000288 PEX7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs3757167 7.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_000292 PHKA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs239748 1.17E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_000297 PKD2 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs2725236 5.00E-06 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_000299 PKP1 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs860554 5.00E-08 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_000299 PKP1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs832147 6.81E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252109 3.07E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs14224 3.04E-19 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252117 3.07E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252120 4.79E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252125 1.55E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252126 1.06E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252130 3.57E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252135 1.09E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1247555 1.91E-13 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1247557 1.63E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1620921 2.67E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1740442 1.63E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2115869 5.38E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs783153 2.04E-15 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1937479 3.04E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2465868 1.54E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000301 PLG 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs935181 9.81E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_000307 POU3F4 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs1410530 4.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_000311 PRNP 19081515 http://www.ncbi.nlm.nih.gov/pubmed/19081515 Creutzfeldt-Jakob Syndrome rs1799990 2.00E-21 Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. NHGRI|-1
NM_000311 PRNP 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs6052699 2.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_000312 PROC 20802025 http://www.ncbi.nlm.nih.gov/pubmed/20802025 Protein C rs1158867 4.00E-36 Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. NHGRI|-1
NM_000315 PTH 19874204 http://www.ncbi.nlm.nih.gov/pubmed/19874204 Bone Density rs9630182 4.00E-07 IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study. NHGRI|-1
NM_000318 PEX2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7821178 3.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_000318 PEX2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs7846385 5.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_000318 PEX2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs3864663 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_000318 PEX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10091852 8.64E-05 NBL-GWAS version 2 dbGaP|2895
NM_000325 PITX2 19597492 http://www.ncbi.nlm.nih.gov/pubmed/19597492 Atrial Fibrillation rs17042171 4.00E-63 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. NHGRI|-1
NM_000325 PITX2 19597491 http://www.ncbi.nlm.nih.gov/pubmed/19597491 Atrial Fibrillation rs2200733 1.00E-14 A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. NHGRI|-1
NM_000325 PITX2 17603472 http://www.ncbi.nlm.nih.gov/pubmed/17603472 Atrial Fibrillation rs2200733 3.00E-41 Variants conferring risk of atrial fibrillation on chromosome 4q25. NHGRI|-1
NM_000325 PITX2 18991354 http://www.ncbi.nlm.nih.gov/pubmed/18991354 Stroke rs2200733 2.00E-10 Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. NHGRI|-1
NM_000325 PITX2 20173747 http://www.ncbi.nlm.nih.gov/pubmed/20173747 Atrial Fibrillation rs6843082 3.00E-28 Common variants in KCNN3 are associated with lone atrial fibrillation. NHGRI|-1
NM_000325 PITX2 17603472 http://www.ncbi.nlm.nih.gov/pubmed/17603472 Atrial Fibrillation rs10033464 7.00E-11 Variants conferring risk of atrial fibrillation on chromosome 4q25. NHGRI|-1
NM_000325 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs10033464 5.70E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_000325 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2654735 9.03E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_000325 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1806506 3.67E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_000331 SAA1 21124955 http://www.ncbi.nlm.nih.gov/pubmed/21124955 Serum Amyloid A Protein rs4638289 3.00E-53 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. NHGRI|-1
NM_000332 ATXN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs3812205 2.44E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_000332 ATXN1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs697739 4.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_000332 ATXN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1573134 5.35E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_000334 SCN4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2227906 1.16E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_000335 SCN5A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs11129795 5.00E-10 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_000335 SCN5A 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs11129795 5.00E-14 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_000335 SCN5A 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12053903 1.00E-14 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_000335 SCN5A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs12053903 1.00E-07 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_000335 SCN5A 19389651 http://www.ncbi.nlm.nih.gov/pubmed/19389651 Electrocardiography rs7638909 2.00E-06 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. NHGRI|-1
NM_000335 SCN5A 21347284 http://www.ncbi.nlm.nih.gov/pubmed/21347284 Electrocardiography rs3922844 3.00E-23 Genome-wide association studies of the PR interval in African Americans. NHGRI|-1
NM_000335 SCN5A 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs11708996 6.00E-26 Genome-wide association study of PR interval. NHGRI|-1
NM_000335 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11708996 7.00E-06 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_000335 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11710077 1.00E-06 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_000335 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9851724 6.00E-16 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_000337 SGCD 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Anthropometry rs157350 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_000337 SGCD 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Waist-Hip Ratio rs157350 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_000337 SGCD 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs4704970 7.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_000340 SLC2A2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs11920090 8.00E-13 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_000340 SLC2A2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs11920090 5.00E-06 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_000345 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs3857059 3.60E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_000345 SNCA 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs2736990 2.00E-16 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_000345 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2736990 5.69E-09 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_000345 SNCA 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs2736990 7.00E-08 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_000345 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356188 8.41E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_000345 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs3775439 4.43E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_000345 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs894278 2.64E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_000345 SNCA 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs6532197 1.00E-07 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_000345 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4106153 9.18E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_000345 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1504489 8.42E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_000345 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12644119 2.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_000345 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356229 5.48E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_000345 SNCA 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs356219 2.00E-47 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_000345 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11931074 4.78E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_000345 SNCA 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson Disease rs11931074 7.00E-17 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_000345 SNCA 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs356220 2.00E-19 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_000345 SNCA 20711177 http://www.ncbi.nlm.nih.gov/pubmed/20711177 Parkinson Disease rs356220 3.00E-11 Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. NHGRI|-1
NM_000345 SNCA 21084426 http://www.ncbi.nlm.nih.gov/pubmed/21084426 Parkinson Disease rs356220 3.00E-08 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. NHGRI|-1
NM_000345 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356220 6.99E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_000345 SNCA 21044948 http://www.ncbi.nlm.nih.gov/pubmed/21044948 Parkinson Disease rs356220 9.00E-16 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. NHGRI|-1
NM_000346 SOX9 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs6501384 6.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_000346 SOX9 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs17779747 6.00E-12 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_000346 SOX9 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs17718586 2.00E-08 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_000346 SOX9 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs17764124 1.45E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_000346 SOX9 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs1859962 1.00E-06 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_000346 SOX9 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs1859962 2.00E-16 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_000346 SOX9 17603485 http://www.ncbi.nlm.nih.gov/pubmed/17603485 Prostatic Neoplasms rs1859962 3.00E-10 "Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes." NHGRI|-1
NM_000346 SOX9 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs1859962 3.00E-11 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_000346 SOX9 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs12451750 1.66E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_000346 SOX9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2193055 7.14E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_000346 SOX9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1558748 5.35E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_000347 SPTB 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs229673 6.70E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_000347 SPTB 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2285002 1.43E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_000350 ABCA4 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs17110736 5.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_000350 ABCA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2297634 3.18E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_000350 ABCA4 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs2774920 1.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_000360 TH 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs7111341 4.00E-48 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_000360 TH 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs7127900 3.00E-33 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_000366 TPM1 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs11071720 2.00E-08 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_000368 TSC1 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs1076160 6.00E-06 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NM_000369 TSHR 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs17111394 4.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_000369 TSHR 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs8017455 6.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_000372 TYR 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Melanosis rs1042602 2.00E-11 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_000372 TYR 17999355 http://www.ncbi.nlm.nih.gov/pubmed/17999355 Skin Pigmentation rs1042602 4.00E-10 A genomewide association study of skin pigmentation in a South Asian population. NHGRI|-1
NM_000372 TYR 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs1847134 1.00E-15 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_000372 TYR 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Eye Color rs1393350 3.00E-12 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_000372 TYR 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs1393350 3.00E-09 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_000372 TYR 19578364 http://www.ncbi.nlm.nih.gov/pubmed/19578364 Melanoma rs1393350 2.00E-14 Genome-wide association study identifies three loci associated with melanoma risk. NHGRI|-1
NM_000372 TYR 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs1393350 2.00E-13 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_000372 TYR 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Suntan rs1393350 2.00E-06 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_000372 TYR 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs1393350 2.00E-18 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_000378 WT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs11031676 5.68E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_000378 WT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7944342 6.98E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_000381 MID1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs5934953 1.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_000381 MID1 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs12388359 4.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_000383 AIRE 21505073 http://www.ncbi.nlm.nih.gov/pubmed/21505073 "Arthritis, Rheumatoid" rs2075876 4.00E-09 The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population. NHGRI|-1
NM_000384 APOB 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs693 1.00E-21 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_000384 APOB 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs693 3.00E-11 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_000384 APOB 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs693 4.00E-17 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000384 APOB 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Cholesterol, LDL" rs693 7.00E-07 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_000384 APOB 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs693 9.00E-23 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000384 APOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs693 2.99E-11 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_000384 APOB 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs693 2.00E-07 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_000384 APOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs673548 3.40E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_000384 APOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs673548 2.28E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_000384 APOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs673548 2.01E-08 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_000384 APOB 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Triglycerides rs673548 2.00E-08 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_000384 APOB 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs515135 2.00E-20 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_000384 APOB 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs515135 5.00E-29 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000384 APOB 18262040 http://www.ncbi.nlm.nih.gov/pubmed/18262040 "Cholesterol, LDL" rs562338 1.00E-09 LDL-cholesterol concentrations: a genome-wide association study. NHGRI|-1
NM_000384 APOB 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs562338 6.00E-22 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_000384 APOB 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, LDL" rs541041 8.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_000384 APOB 20657596 http://www.ncbi.nlm.nih.gov/pubmed/20657596 Hypertriglyceridemia rs4635554 2.00E-07 Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. NHGRI|-1
NM_000384 APOB 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs219553 7.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_000384 APOB 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs1117324 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_000384 APOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10495717 1.31E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_000384 APOB 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1562900 9.25E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_000384 APOB 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs949978 4.94E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_000384 APOB 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs6733000 2.01E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_000384 APOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1605834 5.11E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_000384 APOB 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs13015955 4.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_000384 APOB 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2681019 8.00E-08 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_000384 APOB 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs1449984 7.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_000384 APOB 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs2577720 8.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_000384 APOB 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7569328 1.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_000384 APOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs3923037 2.29E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_000384 APOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs3923037 2.34E-06 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_000384 APOB 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs11902417 4.00E-07 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_000384 APOB 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs6544366 2.00E-07 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_000384 APOB 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, HDL" rs6754295 4.00E-08 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000384 APOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs6754295 3.78E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_000384 APOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs6754295 1.40E-08 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_000384 APOB 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Triglycerides rs6754295 3.00E-08 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000384 APOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs6754295 9.47E-08 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_000384 APOB 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs7557067 9.00E-12 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000388 CASR 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs17251221 2.00E-22 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_000388 CASR 20661308 http://www.ncbi.nlm.nih.gov/pubmed/20661308 Calcium rs1801725 6.00E-37 Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene. NHGRI|-1
NM_000389 CDKN1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs236449 9.40E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_000389 CDKN1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs236448 9.39E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_000389 CDKN1A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs1321311 3.00E-10 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_000389 CDKN1A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9470361 3.00E-27 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_000390 CHM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs242849 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_000404 GLB1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs13314993 3.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_000404 GLB1 21105107 http://www.ncbi.nlm.nih.gov/pubmed/21105107 "Carcinoma, Hepatocellular" rs4678680 2.00E-07 Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma. NHGRI|-1
NM_000408 GPD2 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs7601713 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_000410 HFE 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs1799945 3.00E-09 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_000410 HFE 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs1800562 2.00E-32 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_000410 HFE 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs1800562 1.00E-23 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_000410 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 1.00E-46 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_000410 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Erythrocyte Indices rs1800562 2.00E-08 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_000410 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 3.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_000410 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 6.00E-19 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_000410 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 6.00E-07 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_000410 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs1800562 2.00E-09 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_000410 HFE 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1800562 3.00E-20 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_000410 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Hemoglobins rs1800562 5.00E-07 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_000410 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Iron rs1800562 4.00E-11 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_000410 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 1.00E-10 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_000410 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 4.00E-15 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_000412 HRG 20303064 http://www.ncbi.nlm.nih.gov/pubmed/20303064 Partial Thromboplastin Time rs9898 1.00E-11 "Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time." NHGRI|-1
NM_000412 HRG 20876611 http://www.ncbi.nlm.nih.gov/pubmed/20876611 Adiponectin rs11924390 2.00E-09 Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ. NHGRI|-1
NM_000416 IFNGR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4896243 2.67E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_000417 IL2RA 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs706779 3.00E-09 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_000417 IL2RA 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs706778 1.00E-11 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_000417 IL2RA 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs2104286 7.00E-06 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_000417 IL2RA 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs2104286 9.00E-08 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_000417 IL2RA 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs3118470 2.00E-12 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_000417 IL2RA 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs12722489 3.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_000417 IL2RA 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs12722489 3.00E-08 Risk alleles for multiple sclerosis identified by a genomewide study. NHGRI|-1
NM_000423 KRT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2232559 1.24E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_000426 LAMA2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs17799083 1.88E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_000428 LTBP2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs862034 7.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_000431 MVK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs3759387 9.45E-05 NBL-GWAS version 2 dbGaP|2895
NM_000432 MYL2 21270382 http://www.ncbi.nlm.nih.gov/pubmed/21270382 Alcohol Drinking rs12229654 4.00E-35 Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men. NHGRI|-1
NM_000434 NEU1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9267649 3.11E-126 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_000438 PAX3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs348970 1.96E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_000439 PCSK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9918149 4.77E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_000442 PECAM1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs6504218 1.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_000444 PHEX 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs12559632 3.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_000446 PON1 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 "Arthritis, Rheumatoid" rs854555 2.00E-06 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_000450 SELE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs5359 6.98E-06 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000450 SELE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1076637 1.89E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000450 SELE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3917419 2.43E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000450 SELE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs5353 5.11E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000450 SELE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4656703 4.48E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000450 SELE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3917449 5.35E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000452 SLC10A2 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs912969 8.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_000452 SLC10A2 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Prostatic Neoplasms rs1529276 2.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_000452 SLC10A2 18759275 http://www.ncbi.nlm.nih.gov/pubmed/18759275 Uric Acid rs4771450 2.00E-06 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. NHGRI|-1
NM_000452 SLC10A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1331519 9.12E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_000452 SLC10A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1757387 7.90E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_000452 SLC10A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1757387 9.13E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_000456 SUOX 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs1701704 3.00E-08 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_000456 SUOX 18198356 http://www.ncbi.nlm.nih.gov/pubmed/18198356 "Diabetes Mellitus, Type 1" rs1701704 9.00E-10 A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study. NHGRI|-1
NM_000457 HNF4A 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs1800961 8.00E-10 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000457 HNF4A 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs1800961 2.00E-09 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_000457 HNF4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs1800961 7.13E-07 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_000457 HNF4A 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6017342 1.00E-20 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_000457 HNF4A 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs6017342 9.00E-17 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_000458 HNF1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2107133 8.77E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_000458 HNF1B 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs4430796 2.00E-06 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_000458 HNF1B 21499250 http://www.ncbi.nlm.nih.gov/pubmed/21499250 Endometrial Neoplasms rs4430796 7.00E-10 Genome-wide association study identifies a common variant associated with risk of endometrial cancer. NHGRI|-1
NM_000458 HNF1B 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs4430796 6.00E-11 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_000458 HNF1B 17603485 http://www.ncbi.nlm.nih.gov/pubmed/17603485 Prostatic Neoplasms rs4430796 1.00E-11 "Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes." NHGRI|-1
NM_000458 HNF1B 18264096 http://www.ncbi.nlm.nih.gov/pubmed/18264096 Prostatic Neoplasms rs4430796 1.00E-09 Multiple loci identified in a genome-wide association study of prostate cancer. NHGRI|-1
NM_000458 HNF1B 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs4430796 8.00E-06 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_000458 HNF1B 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs7501939 1.00E-12 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_000458 HNF1B 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs7501939 2.00E-06 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_000458 HNF1B 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs7501939 3.00E-18 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_000458 HNF1B 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs7501939 9.00E-12 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_000461 THRB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs9310736 3.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_000461 THRB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs9310736 4.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_000461 THRB 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs3903470 8.59E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_000462 UBE3A 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs17636733 2.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_000462 UBE3A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2930629 5.39E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_000463 UGT1A1 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs887829 1.00E-69 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_000463 UGT1A1 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs6742078 5E-324 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_000463 UGT1A1 21646302 http://www.ncbi.nlm.nih.gov/pubmed/21646302 Bilirubin rs4148325 5.00E-62 Mayo genome consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. NHGRI|-1
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs16852600 6.83E-05 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs895459 1.11E-05 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2053710 1.62E-06 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1374230 1.62E-05 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10932572 2.84E-05 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7584646 3.73E-05 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7557557 1.42E-06 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 21124317 http://www.ncbi.nlm.nih.gov/pubmed/21124317 Neuroblastoma rs3768716 5.00E-13 Integrative genomics identifies LMO1 as a neuroblastoma oncogene. NHGRI|-1
NM_000465 BARD1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs3768716 6.35E-06 NBL-GWAS version 1 dbGaP|2845
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs3768716 7.25E-13 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs17487792 1.35E-12 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7587476 3.05E-13 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6712055 2.17E-09 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6435862 2.93E-09 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 19412175 http://www.ncbi.nlm.nih.gov/pubmed/19412175 Neuroblastoma rs6435862 9.00E-18 Common variations in BARD1 influence susceptibility to high-risk neuroblastoma. NHGRI|-1
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6715570 1.21E-09 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6744811 4.72E-07 NBL-GWAS version 2 dbGaP|2895
NM_000465 BARD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2121283 4.19E-06 NBL-GWAS version 2 dbGaP|2895
NM_000476 AK1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Blood Pressure rs7865146 1.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_000478 ALPL 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs1780324 7.00E-15 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_000478 ALPL 20558539 http://www.ncbi.nlm.nih.gov/pubmed/20558539 Phosphorus rs1697421 1.00E-27 Common genetic variants associate with serum phosphorus concentration. NHGRI|-1
NM_000480 AMPD3 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Bipolar Disorder rs6484218 4.00E-08 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_000482 APOA4 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs1263173 2.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_000482 APOA4 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Triglycerides rs7396835 1.00E-09 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_000487 ARSA 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs9616906 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_000494 COL17A1 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1320448 2.00E-08 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_000499 CYP1A1 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs2470893 5.00E-14 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_000499 CYP1A1 21357676 http://www.ncbi.nlm.nih.gov/pubmed/21357676 Coffee rs2472297 5.00E-14 Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption. NHGRI|-1
NM_000499 CYP1A1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs2472299 3.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_000503 EYA1 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs2218488 3.00E-06 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_000505 F12 21546496 http://www.ncbi.nlm.nih.gov/pubmed/21546496 Blood Platelets rs2731672 1.00E-06 Novel loci involved on platelet function and platelet count identified by a genome-wide study performed in children. NHGRI|-1
NM_000505 F12 20303064 http://www.ncbi.nlm.nih.gov/pubmed/20303064 Partial Thromboplastin Time rs2731672 2.00E-30 "Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time." NHGRI|-1
NM_000508 FGA 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs13109457 3.00E-18 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_000509 FGG 18823527 http://www.ncbi.nlm.nih.gov/pubmed/18823527 Alzheimer Disease rs727153 3.00E-06 A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. NHGRI|-1
NM_000509 FGG 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs13109457 3.00E-18 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_000511 FUT2 18776911 http://www.ncbi.nlm.nih.gov/pubmed/18776911 Vitamin B 12 rs492602 5.00E-17 Common variants of FUT2 are associated with plasma vitamin B12 levels. NHGRI|-1
NM_000511 FUT2 19303062 http://www.ncbi.nlm.nih.gov/pubmed/19303062 Vitamin B 12 rs602662 3.00E-20 "Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations." NHGRI|-1
NM_000511 FUT2 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs504963 2.00E-08 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_000511 FUT2 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs281379 7.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_000514 GDNF 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs270545 1.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_000516 GNAS 21046636 http://www.ncbi.nlm.nih.gov/pubmed/21046636 Brain Waves rs13831 6.00E-06 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. NHGRI|-1
NM_000518 HBB 19465909 http://www.ncbi.nlm.nih.gov/pubmed/19465909 Malaria rs11036238 4.00E-11 Genome-wide and fine-resolution association analysis of malaria in West Africa. NHGRI|-1
NM_000524 HTR1A 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs255414 1.00E-06 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_000525 KCNJ11 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs5215 4.00E-07 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_000525 KCNJ11 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs5215 5.00E-11 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_000525 KCNJ11 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs5219 1.00E-07 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_000525 KCNJ11 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs5219 1.00E-09 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_000525 KCNJ11 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs5219 5.00E-07 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_000525 KCNJ11 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs5219 7.00E-11 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_000527 LDLR 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs6511720 2.00E-26 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000527 LDLR 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs6511720 2.00E-51 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_000527 LDLR 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs6511720 4.00E-26 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_000527 LDLR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs2228671 4.00E-14 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000527 LDLR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs2228671 9.00E-24 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000527 LDLR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs2228671 2.34E-06 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_000527 LDLR 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs2738459 7.00E-06 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_000527 LDLR 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs11668477 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_000527 LDLR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs11668477 1.51E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_000532 PCCB 20031576 http://www.ncbi.nlm.nih.gov/pubmed/20031576 Fibrinogen rs511154 6.00E-10 Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. NHGRI|-1
NM_000541 SAG 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1000141 2.30E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs16870907 2.46E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241453 3.04E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241452 2.07E-72 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241448 7.86E-70 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241447 4.69E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241440 2.36E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1015166 8.68E-107 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241427 3.48E-82 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_000544 TAP2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs241427 1.66E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241425 1.60E-94 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241424 7.96E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1894406 9.40E-88 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2857106 2.39E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9784758 6.79E-77 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_000544 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9784758 2.30E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_000545 HNF1A 19567438 http://www.ncbi.nlm.nih.gov/pubmed/19567438 C-Reactive Protein rs1183910 1.00E-30 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. NHGRI|-1
NM_000545 HNF1A 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs1183910 2.00E-124 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_000545 HNF1A 21196492 http://www.ncbi.nlm.nih.gov/pubmed/21196492 C-Reactive Protein rs7310409 3.00E-08 Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus. NHGRI|-1
NM_000545 HNF1A 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs7310409 7.00E-17 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_000545 HNF1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7310409 4.36E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_000545 HNF1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7310409 8.56E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_000545 HNF1A 19198612 http://www.ncbi.nlm.nih.gov/pubmed/19198612 Coronary Artery Disease rs2259816 5.00E-07 New susceptibility locus for coronary artery disease on chromosome 3q22.3. NHGRI|-1
NM_000545 HNF1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs735396 2.13E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_000545 HNF1A 18439552 http://www.ncbi.nlm.nih.gov/pubmed/18439552 C-Reactive Protein rs1169310 2.00E-08 Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein. NHGRI|-1
NM_000548 TSC2 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs2516739 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_000550 TYRP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12379024 3.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_000550 TYRP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs13288636 5.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_000550 TYRP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs13288681 7.20E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_000550 TYRP1 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs1325154 5.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_000550 TYRP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10809811 3.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_000550 TYRP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1121541 3.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_000550 TYRP1 18488028 http://www.ncbi.nlm.nih.gov/pubmed/18488028 Eye Color rs1408799 6.00E-17 Two newly identified genetic determinants of pigmentation in Europeans. NHGRI|-1
NM_000550 TYRP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10809826 1.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_000553 WRN 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 Exercise Test rs2553268 6.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_000560 CD53 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7513168 1.49E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000560 CD53 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1282020 8.95E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_000560 CD53 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1282023 8.95E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_000560 CD53 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1548342 8.72E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_000560 CD53 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6701134 6.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_000565 IL6R 19567438 http://www.ncbi.nlm.nih.gov/pubmed/19567438 C-Reactive Protein rs4537545 2.00E-14 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. NHGRI|-1
NM_000565 IL6R 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4129267 2.00E-48 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_000565 IL6R 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Maximal Midexpiratory Flow Rate rs4129267 7.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_000565 IL6R 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 "Receptors, Interleukin-6" rs4129267 2.00E-57 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_000565 IL6R 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs2228145 2.00E-08 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_000565 IL6R 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs2228145 2.00E-11 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_000567 CRP 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs3091244 6.00E-28 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_000567 CRP 21196492 http://www.ncbi.nlm.nih.gov/pubmed/21196492 C-Reactive Protein rs3093059 4.00E-21 Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus. NHGRI|-1
NM_000567 CRP 19567438 http://www.ncbi.nlm.nih.gov/pubmed/19567438 C-Reactive Protein rs7553007 8.00E-44 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. NHGRI|-1
NM_000567 CRP 18439552 http://www.ncbi.nlm.nih.gov/pubmed/18439552 C-Reactive Protein rs11265260 7.00E-06 Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein. NHGRI|-1
NM_000567 CRP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs11265260 4.45E-09 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_000567 CRP 21396408 http://www.ncbi.nlm.nih.gov/pubmed/21396408 Vaccination rs11265263 3.00E-06 Atopy history and the genomics of wheezing after influenza vaccination in children 6-59 months of age. NHGRI|-1
NM_000567 CRP 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs2794520 2.00E-186 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_000567 CRP 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs2794520 3.00E-08 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_000567 CRP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs2794520 2.92E-22 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_000567 CRP 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Inflammation rs2794520 3.00E-22 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_000567 CRP 18385676 http://www.ncbi.nlm.nih.gov/pubmed/18385676 Lung Neoplasms rs2808630 7.00E-06 Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. NHGRI|-1
NM_000572 IL10 20228798 http://www.ncbi.nlm.nih.gov/pubmed/20228798 "Colitis, Ulcerative" rs3024493 1.00E-12 Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). NHGRI|-1
NM_000572 IL10 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs3024493 8.00E-08 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_000572 IL10 20622878 http://www.ncbi.nlm.nih.gov/pubmed/20622878 Behcet Syndrome rs1518111 4.00E-18 "Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behtet's disease." NHGRI|-1
NM_000572 IL10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3024490 2.22E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_000572 IL10 20622879 http://www.ncbi.nlm.nih.gov/pubmed/20622879 Behcet Syndrome rs1800871 1.00E-14 Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behtet's disease susceptibility loci. NHGRI|-1
NM_000572 IL10 18836448 http://www.ncbi.nlm.nih.gov/pubmed/18836448 "Colitis, Ulcerative" rs3024505 1.00E-12 "Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility." NHGRI|-1
NM_000572 IL10 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs3024505 1.00E-08 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_000572 IL10 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs3024505 6.00E-17 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_000572 IL10 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs3024505 2.00E-14 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_000572 IL10 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs3024505 2.00E-09 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_000573 CR1 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs3818361 4.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_000573 CR1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs6701713 5.00E-10 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_000573 CR1 21700265 http://www.ncbi.nlm.nih.gov/pubmed/21700265 Blood Sedimentation rs12034383 2.00E-28 Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. NHGRI|-1
NM_000573 CR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs12034383 1.65E-05 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_000575 IL1A 20844546 http://www.ncbi.nlm.nih.gov/pubmed/20844546 Endometriosis rs6542095 3.00E-06 Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population. NHGRI|-1
NM_000575 IL1A 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11677416 7.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_000577 IL1RN 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs6734238 2.00E-17 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_000579 CCR5 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs6441975 5.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_000582 SPP1 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs2725236 5.00E-06 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_000583 GC 20541252 http://www.ncbi.nlm.nih.gov/pubmed/20541252 Vitamin D rs2282679 2.00E-109 Common genetic determinants of vitamin D insufficiency: a genome-wide association study. NHGRI|-1
NM_000583 GC 20418485 http://www.ncbi.nlm.nih.gov/pubmed/20418485 Vitamin D rs2282679 2.00E-49 Genome-wide association study of circulating vitamin D levels. NHGRI|-1
NM_000585 IL15 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs17007695 9.00E-07 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_000585 IL15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs746484 6.98E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_000585 IL15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9308140 5.26E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_000585 IL15 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4267812 6.73E-06 NBL-GWAS version 1 dbGaP|2845
NM_000586 IL2 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs6852535 1.00E-07 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_000586 IL2 17558408 http://www.ncbi.nlm.nih.gov/pubmed/17558408 Celiac Disease rs6822844 1.00E-14 A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21. NHGRI|-1
NM_000586 IL2 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs6822844 3.00E-13 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_000586 IL2 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs7682241 4.00E-08 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_000593 TAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2071540 1.26E-69 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_000594 TNF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3093662 4.75E-21 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_000595 LTA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2009658 6.64E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_000595 LTA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2229094 1.68E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_000595 LTA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112071469 2.90E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_000598 IGFBP3 21216879 http://www.ncbi.nlm.nih.gov/pubmed/21216879 Insulin-Like Growth Factor Binding Protein 3 rs11977526 3.00E-101 A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. NHGRI|-1
NM_000600 IL6 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs10229203 1.95E-06 NBL-GWAS version 1 dbGaP|2845
NM_000600 IL6 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1989838 9.78E-07 NBL-GWAS version 1 dbGaP|2845
NM_000600 IL6 21196492 http://www.ncbi.nlm.nih.gov/pubmed/21196492 C-Reactive Protein rs2097677 4.00E-11 Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus. NHGRI|-1
NM_000601 HGF 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs4236644 2.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_000609 CXCL12 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs501120 9.00E-08 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_000609 CXCL12 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs1746048 3.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_000609 CXCL12 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs1746048 7.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_000610 CD44 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2295756 9.65E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_000612 IGF2 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs3741208 2.00E-07 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_000612 IGF2 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 "Diabetes Mellitus, Type 1" rs1004446 4.00E-09 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NM_000615 NCAM1 21212386 http://www.ncbi.nlm.nih.gov/pubmed/21212386 Blood Vessels rs1436109 3.00E-07 Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. NHGRI|-1
NM_000615 NCAM1 21212386 http://www.ncbi.nlm.nih.gov/pubmed/21212386 Blood Vessels rs1436109 4.00E-09 Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. NHGRI|-1
NM_000615 NCAM1 21212386 http://www.ncbi.nlm.nih.gov/pubmed/21212386 Blood Vessels rs1436109 9.00E-07 Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. NHGRI|-1
NM_000615 NCAM1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs12279261 9.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_000615 NCAM1 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs7105881 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_000618 IGF1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs5742692 4.00E-08 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_000618 IGF1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs35767 3.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_000618 IGF1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Insulin Resistance rs35767 2.00E-09 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_000618 IGF1 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs2172873 2.00E-06 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_000618 IGF1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs1520223 9.00E-07 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_000619 IFNG 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs7134599 1.00E-16 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_000619 IFNG 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs1558744 3.00E-12 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_000619 IFNG 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs1558744 4.00E-12 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_000620 NOS1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs478597 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_000625 NOS2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2297515 2.13E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_000625 NOS2 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs4795067 4.00E-11 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_000627 LTBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4670322 5.13E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_000627 LTBP1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs3769528 8.00E-08 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_000627 LTBP1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs41464348 7.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_000631 NCF4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4821544 1.71E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_000632 ITGAM 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs9888739 1.00E-15 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_000632 ITGAM 18204446 http://www.ncbi.nlm.nih.gov/pubmed/18204446 "Lupus Erythematosus, Systemic" rs9888739 2.00E-23 "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci." NHGRI|-1
NM_000632 ITGAM 19165918 http://www.ncbi.nlm.nih.gov/pubmed/19165918 "Lupus Erythematosus, Systemic" rs11150610 2.00E-06 Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. NHGRI|-1
NM_000634 CXCR1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs11676348 1.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_000635 RFX2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11880706 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_000636 SOD2 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs4516970 1.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_000639 FASLG 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs859637 2.00E-06 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_000639 FASLG 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs9286879 2.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_000639 FASLG 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs12035082 2.00E-07 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_000639 FASLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2859242 6.73E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000641 IL11 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs1126757 3.00E-06 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_000642 AGL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs17121644 4.78E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000643 AGL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs17121644 4.78E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000644 AGL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs17121644 4.78E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000645 AGL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs17121644 4.78E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000646 AGL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs17121644 4.78E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000651 CR1 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs3818361 4.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_000651 CR1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs6701713 5.00E-10 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_000651 CR1 21700265 http://www.ncbi.nlm.nih.gov/pubmed/21700265 Blood Sedimentation rs12034383 2.00E-28 Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. NHGRI|-1
NM_000651 CR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs12034383 1.65E-05 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_000655 SELL 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12938 6.33E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_000655 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs964555 2.34E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000655 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4987314 1.23E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000655 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2229569 9.88E-06 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000655 SELL 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs1131498 4.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_000655 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4987285 6.00E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000655 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2205849 1.40E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000655 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4656703 4.48E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000655 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3917449 5.35E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000655 SELL 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs1569476 3.00E-07 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_000658 AIRE 21505073 http://www.ncbi.nlm.nih.gov/pubmed/21505073 "Arthritis, Rheumatoid" rs2075876 4.00E-09 The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population. NHGRI|-1
NM_000662 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 2.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_000662 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 4.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_000662 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 8.00E-08 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_000665 ACHE 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs7636 5.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_000668 ADH1B 19698717 http://www.ncbi.nlm.nih.gov/pubmed/19698717 Esophageal Neoplasms rs1229984 8.00E-24 Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk. NHGRI|-1
NM_000668 ADH1B 21437268 http://www.ncbi.nlm.nih.gov/pubmed/21437268 Head and Neck Neoplasms rs1229984 1.00E-20 A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. NHGRI|-1
NM_000668 ADH1B 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs1789891 3.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_000669 ADH1C 21437268 http://www.ncbi.nlm.nih.gov/pubmed/21437268 Head and Neck Neoplasms rs1789924 3.00E-07 A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. NHGRI|-1
NM_000669 ADH1C 19609347 http://www.ncbi.nlm.nih.gov/pubmed/19609347 Hypertension rs991316 5.00E-06 A genome-wide association study of hypertension and blood pressure in African Americans. NHGRI|-1
NM_000669 ADH1C 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs1789891 3.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_000673 ADH7 21437268 http://www.ncbi.nlm.nih.gov/pubmed/21437268 Head and Neck Neoplasms rs971074 9.00E-17 A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. NHGRI|-1
NM_000673 ADH7 19609347 http://www.ncbi.nlm.nih.gov/pubmed/19609347 Hypertension rs991316 5.00E-06 A genome-wide association study of hypertension and blood pressure in African Americans. NHGRI|-1
NM_000674 ADORA1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs16851020 4.14E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_000677 ADORA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10857899 3.06E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_000677 ADORA3 20548944 http://www.ncbi.nlm.nih.gov/pubmed/20548944 Bone Density rs494453 4.00E-08 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. NHGRI|-1
NM_000678 ADRA1D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4813680 8.33E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000678 ADRA1D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs8115863 8.33E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000678 ADRA1D 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs16989303 6.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_000679 ADRA1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs952037 8.24E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_000679 ADRA1B 20953188 http://www.ncbi.nlm.nih.gov/pubmed/20953188 Psoriasis rs2546890 1.00E-20 Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. NHGRI|-1
NM_000679 ADRA1B 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs10045431 4.00E-13 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_000679 ADRA1B 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs10045431 7.00E-08 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_000679 ADRA1B 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs6556416 2.00E-08 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_000679 ADRA1B 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs6887695 9.00E-06 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_000679 ADRA1B 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6871626 1.00E-21 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_000679 ADRA1B 20953186 http://www.ncbi.nlm.nih.gov/pubmed/20953186 "Arthritis, Psoriatic" rs12188300 7.00E-17 Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. NHGRI|-1
NM_000681 ADRA2A 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs869244 3.00E-12 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_000681 ADRA2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1335706 1.27E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_000681 ADRA2A 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs10885122 3.00E-16 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_000681 ADRA2A 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs10885122 2.00E-06 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_000681 ADRA2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4342958 7.51E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_000683 ADRA2C 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs28523451 3.08E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_000686 AGTR2 21602797 http://www.ncbi.nlm.nih.gov/pubmed/21602797 Cystic Fibrosis rs1403543 2.00E-06 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. NHGRI|-1
NM_000689 ALDH1A1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4237255 5.02E-06 NBL-GWAS version 1 dbGaP|2845
NM_000690 ALDH2 21372407 http://www.ncbi.nlm.nih.gov/pubmed/21372407 Drinking Behavior rs671 4.00E-211 Confirmation of ALDH2 as a Major locus of drinking behavior and of its variants regulating multiple metabolic phenotypes in a Japanese population. NHGRI|-1
NM_000690 ALDH2 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs671 7.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_000690 ALDH2 19698717 http://www.ncbi.nlm.nih.gov/pubmed/19698717 Esophageal Neoplasms rs671 3.00E-24 Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk. NHGRI|-1
NM_000690 ALDH2 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 gamma-Glutamyltransferase rs671 5.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_000698 ALOX5 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs7090328 6.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_000700 ANXA1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs11143609 7.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_000700 ANXA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1398307 5.92E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_000700 ANXA1 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Bipolar Disorder rs3758354 3.00E-06 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_000701 ATP1A1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7552721 5.96E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_000705 ATP4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12020712 6.75E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_000716 C4BPB 20212171 http://www.ncbi.nlm.nih.gov/pubmed/20212171 Complement C4b-Binding Protein rs3813948 4.00E-10 C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies. NHGRI|-1
NM_000719 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_000719 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_000719 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_000719 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_000722 CACNA2D1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs10954668 7.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_000722 CACNA2D1 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Mortality rs2371208 3.00E-06 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_000724 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 1.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_000724 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 7.00E-07 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_000724 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs11014166 6.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_000724 CACNB2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Blood Pressure rs7069923 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_000724 CACNB2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 C-Reactive Protein rs7076247 6.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_000724 CACNB2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17661538 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_000724 CACNB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4748442 9.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_000733 CD3E 19207018 http://www.ncbi.nlm.nih.gov/pubmed/19207018 Pain Measurement rs17122021 7.00E-07 Genome-wide association study of acute post-surgical pain in humans. NHGRI|-1
NM_000734 CD247 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs840016 2.00E-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_000734 CD247 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs864537 2.00E-11 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_000734 CD247 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs864537 4.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_000734 CD247 20383147 http://www.ncbi.nlm.nih.gov/pubmed/20383147 "Scleroderma, Systemic" rs2056626 3.00E-09 Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. NHGRI|-1
NM_000734 CD247 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs2056626 1.00E-06 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_000740 CHRM3 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Hypertension rs2820037 8.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_000740 CHRM3 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs6677208 3.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_000743 CHRNA3 18978790 http://www.ncbi.nlm.nih.gov/pubmed/18978790 Lung Neoplasms rs1051730 1.00E-15 Lung cancer susceptibility locus at 5p15.33. NHGRI|-1
NM_000743 CHRNA3 19836008 http://www.ncbi.nlm.nih.gov/pubmed/19836008 Lung Neoplasms rs1051730 2.00E-51 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. NHGRI|-1
NM_000743 CHRNA3 20418889 http://www.ncbi.nlm.nih.gov/pubmed/20418889 Smoking rs1051730 2.00E-66 Meta-analysis and imputation refines the association of 15q25 with smoking quantity. NHGRI|-1
NM_000743 CHRNA3 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs1051730 2.00E-69 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_000743 CHRNA3 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs1051730 3.00E-73 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_000743 CHRNA3 18385739 http://www.ncbi.nlm.nih.gov/pubmed/18385739 Tobacco Use Disorder rs1051730 6.00E-20 "A variant associated with nicotine dependence, lung cancer and peripheral arterial disease." NHGRI|-1
NM_000743 CHRNA3 18978787 http://www.ncbi.nlm.nih.gov/pubmed/18978787 Lung Neoplasms rs8042374 8.00E-12 Common 5p15.33 and 6p21.33 variants influence lung cancer risk. NHGRI|-1
NM_000746 CHRNA7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4779984 1.58E-05 NBL-GWAS version 2 dbGaP|2895
NM_000746 CHRNA7 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1001555 3.75E-06 NBL-GWAS version 1 dbGaP|2845
NM_000749 CHRNB3 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs6474412 1.00E-08 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_000750 CHRNB4 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs950776 4.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_000757 CSF1 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs10494112 7.00E-35 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_000757 CSF1 20436471 http://www.ncbi.nlm.nih.gov/pubmed/20436471 Osteitis Deformans rs484959 5.00E-24 "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone." NHGRI|-1
NM_000757 CSF1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs525566 5.88E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_000759 CSF3 20172861 http://www.ncbi.nlm.nih.gov/pubmed/20172861 Leukocyte Count rs4794822 6.00E-10 Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count. NHGRI|-1
NM_000759 CSF3 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs4794822 4.00E-16 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_000760 CSF3R 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7549591 7.93E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_000761 CYP1A2 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs2472304 3.00E-07 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_000761 CYP1A2 21357676 http://www.ncbi.nlm.nih.gov/pubmed/21357676 Coffee rs2472297 5.00E-14 Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption. NHGRI|-1
NM_000761 CYP1A2 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs2472299 3.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_000762 CYP2A6 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs4105144 2.00E-12 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_000764 CYP2A7 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs4105144 2.00E-12 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_000767 CYP2B6 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs7260329 6.00E-06 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_000769 CYP2C19 19578179 http://www.ncbi.nlm.nih.gov/pubmed/19578179 Acenocoumarol rs12767583 3.00E-07 A genome-wide association study of acenocoumarol maintenance dosage. NHGRI|-1
NM_000770 CYP2C8 18594024 http://www.ncbi.nlm.nih.gov/pubmed/18594024 Osteonecrosis rs1934951 1.00E-06 Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis. NHGRI|-1
NM_000770 CYP2C8 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs2185570 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_000771 CYP2C9 19300499 http://www.ncbi.nlm.nih.gov/pubmed/19300499 Warfarin rs1799853 1.00E-31 "A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose." NHGRI|-1
NM_000771 CYP2C9 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs4086116 6.00E-12 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_000771 CYP2C9 20833655 http://www.ncbi.nlm.nih.gov/pubmed/20833655 Warfarin rs10509680 4.00E-07 Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. NHGRI|-1
NM_000771 CYP2C9 19300499 http://www.ncbi.nlm.nih.gov/pubmed/19300499 Warfarin rs1057910 3.00E-79 "A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose." NHGRI|-1
NM_000771 CYP2C9 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs2185570 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_000772 CYP2C18 19578179 http://www.ncbi.nlm.nih.gov/pubmed/19578179 Acenocoumarol rs12772169 8.00E-12 A genome-wide association study of acenocoumarol maintenance dosage. NHGRI|-1
NM_000772 CYP2C18 19706858 http://www.ncbi.nlm.nih.gov/pubmed/19706858 Ticlopidine rs12777823 2.00E-13 Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy. NHGRI|-1
NM_000779 CYP4B1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11583588 6.44E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_000785 CYP27B1 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs703842 5.00E-11 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_000787 DBH 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs3025343 4.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_000789 ACE 20066004 http://www.ncbi.nlm.nih.gov/pubmed/20066004 Angiotensin-Converting Enzyme Inhibitors rs4343 3.00E-25 A genome-wide association study identifies new loci for ACE activity: potential implications for response to ACE inhibitor. NHGRI|-1
NM_000790 DDC 19465909 http://www.ncbi.nlm.nih.gov/pubmed/19465909 Malaria rs1451375 6.00E-06 Genome-wide and fine-resolution association analysis of malaria in West Africa. NHGRI|-1
NM_000794 DRD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs5326 2.49E-05 NBL-GWAS version 2 dbGaP|2895
NM_000794 DRD1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs11134893 2.24E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_000795 DRD2 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Atrial Natriuretic Factor rs1079596 3.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_000795 DRD2 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11214606 5.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_000800 FGF1 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs152528 8.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_000814 GABRB3 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs8043440 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_000814 GABRB3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs3212335 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_000817 GAD1 18759275 http://www.ncbi.nlm.nih.gov/pubmed/18759275 Uric Acid rs4668338 3.00E-06 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. NHGRI|-1
NM_000819 GART 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8971 6.96E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_000819 GART 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2834232 6.96E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_000827 GRIA1 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Height rs12658202 9.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_000827 GRIA1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs12189362 3.00E-10 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_000829 GRIA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10895889 7.40E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_000830 GRIK1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs363512 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_000830 GRIK1 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs458685 6.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_000831 GRIK3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7549591 7.93E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_000833 GRIN2A 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs8050385 1.90E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_000833 GRIN2A 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs1463132 8.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_000833 GRIN2A 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs17550532 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_000834 GRIN2B 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs2160519 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_000834 GRIN2B 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs4764039 3.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_000834 GRIN2B 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs3764030 2.35E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_000840 GRM3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6972995 9.07E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_000842 GRM5 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs16914280 3.00E-07 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_000842 GRM5 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs10831496 5.00E-09 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_000844 GRM7 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs3749380 2.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_000844 GRM7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs10510351 3.30E-04 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_000844 GRM7 21368711 http://www.ncbi.nlm.nih.gov/pubmed/21368711 Personality rs13080594 8.00E-07 Genome-wide association study of personality traits in bipolar patients. NHGRI|-1
NM_000844 GRM7 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs9870680 1.00E-06 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_000844 GRM7 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Factor VII rs4591494 9.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_000845 GRM8 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Carotid Artery Diseases rs17691394 9.00E-07 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_000845 GRM8 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs11971186 9.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NM_000845 GRM8 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs17864092 6.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_000852 GSTP1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4930431 5.65E-06 NBL-GWAS version 1 dbGaP|2845
NM_000855 GUCY1A2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs10895959 3.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_000859 HMGCR 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs12654264 1.00E-20 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_000859 HMGCR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs3846662 2.00E-11 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000859 HMGCR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs3846662 3.00E-19 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000859 HMGCR 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 "Cholesterol, LDL" rs3846663 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_000859 HMGCR 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs3846663 8.00E-12 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000859 HMGCR 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Cholesterol rs3846663 6.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_000859 HMGCR 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs12916 1.00E-11 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_000859 HMGCR 18802019 http://www.ncbi.nlm.nih.gov/pubmed/18802019 "Cholesterol, LDL" rs7703051 1.00E-08 Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. NHGRI|-1
NM_000860 HPGD 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs6852435 6.00E-06 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_000865 HTR1E 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs493187 3.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_000868 HTR2C 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2905404 2.67E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_000868 HTR2C 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2905403 4.66E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_000868 HTR2C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7876428 1.04E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_000868 HTR2C 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs3007183 1.15E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_000870 HTR4 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs11168048 1.00E-11 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_000870 HTR4 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs3995090 4.00E-09 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_000872 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs699213 9.06E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_000872 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12259754 3.59E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_000872 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11186286 3.84E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_000872 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11186286 7.40E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_000872 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11817364 6.36E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_000875 IGF1R 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2871865 3.00E-21 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_000875 IGF1R 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4966017 6.40E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_000876 IGF2R 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs6917747 7.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_000876 IGF2R 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs8191818 3.11E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000876 IGF2R 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs8191829 3.39E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000876 IGF2R 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7753051 1.14E-12 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000877 IL1R1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2310173 3.00E-12 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_000877 IL1R1 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs2310173 5.00E-07 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_000878 IL2RB 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs2284033 1.00E-08 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_000878 IL2RB 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Arthritis, Rheumatoid" rs743777 1.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_000878 IL2RB 21653640 http://www.ncbi.nlm.nih.gov/pubmed/21653640 "Arthritis, Rheumatoid" rs743777 2.00E-06 Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways. NHGRI|-1
NM_000878 IL2RB 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs229492 7.75E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_000879 IL5 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4705952 1.00E-08 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_000879 IL5 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Eosinophils rs4143832 1.00E-10 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_000880 IL7 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs2717536 1.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_000880 IL7 19081515 http://www.ncbi.nlm.nih.gov/pubmed/19081515 Creutzfeldt-Jakob Syndrome rs1460163 6.00E-08 Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. NHGRI|-1
NM_000882 IL12A 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs6441286 2.00E-14 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_000882 IL12A 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs6441286 8.00E-12 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_000882 IL12A 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs485499 2.00E-16 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_000882 IL12A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs17810546 1.49E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_000882 IL12A 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs17810546 1.00E-09 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_000882 IL12A 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs17810546 4.00E-28 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_000882 IL12A 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs4680534 6.00E-06 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_000885 ITGA4 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs12988934 2.00E-14 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_000885 ITGA4 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs13010713 5.00E-11 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_000885 ITGA4 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs1018326 2.00E-06 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_000885 ITGA4 21041692 http://www.ncbi.nlm.nih.gov/pubmed/21041692 Heart Function Tests rs7602460 6.00E-06 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. NHGRI|-1
NM_000887 ITGAX 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs11574637 3.00E-11 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_000888 ITGB6 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10497212 8.49E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_000891 KCNJ2 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs8079702 1.00E-14 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_000891 KCNJ2 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs8079702 4.00E-22 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_000893 KNG1 20303064 http://www.ncbi.nlm.nih.gov/pubmed/20303064 Partial Thromboplastin Time rs710446 1.00E-21 "Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time." NHGRI|-1
NM_000893 KNG1 20876611 http://www.ncbi.nlm.nih.gov/pubmed/20876611 Adiponectin rs11924390 2.00E-09 Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ. NHGRI|-1
NM_000895 LTA4H 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs2660869 3.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_000898 MAOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10521432 8.09E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_000898 MAOB 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs3027409 7.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_000899 KITLG 19483681 http://www.ncbi.nlm.nih.gov/pubmed/19483681 Testicular Neoplasms rs995030 1.00E-31 A genome-wide association study of testicular germ cell tumor. NHGRI|-1
NM_000899 KITLG 19483681 http://www.ncbi.nlm.nih.gov/pubmed/19483681 Testicular Neoplasms rs995030 3.00E-30 A genome-wide association study of testicular germ cell tumor. NHGRI|-1
NM_000899 KITLG 20543847 http://www.ncbi.nlm.nih.gov/pubmed/20543847 Testicular Neoplasms rs3782181 2.00E-26 "Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer." NHGRI|-1
NM_000899 KITLG 19483682 http://www.ncbi.nlm.nih.gov/pubmed/19483682 Testicular Neoplasms rs4474514 6.00E-15 Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer. NHGRI|-1
NM_000899 KITLG 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Hair Color rs12821256 4.00E-30 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_000899 KITLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7960664 9.96E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_000901 NR3C2 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Fibrinogen rs1490453 3.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_000905 NPY 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2529059 3.32E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_000910 NPY2R 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7684755 5.20E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_000912 OPRK1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs10958369 2.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_000912 OPRK1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs360968 1.32E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_000912 OPRK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1426562 3.34E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_000912 OPRK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs6473783 5.28E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_000914 OPRM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs675026 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_000914 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4598087 1.11E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000914 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754521 9.74E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000914 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2186140 5.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_000914 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10499276 8.08E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_000919 PAM 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs1502844 1.00E-06 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_000921 PDE3A 19478329 http://www.ncbi.nlm.nih.gov/pubmed/19478329 "Infertility, Male" rs10841496 5.00E-07 Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. NHGRI|-1
NM_000921 PDE3A 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs1348582 1.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_000921 PDE3A 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs11611208 2.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_000921 PDE3A 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs10770612 2.00E-08 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_000932 PLCB3 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs2244621 5.00E-10 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_000933 PLCB4 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs6039424 9.55E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_000933 PLCB4 20172861 http://www.ncbi.nlm.nih.gov/pubmed/20172861 Leukocyte Count rs2072910 3.00E-10 Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count. NHGRI|-1
NM_000934 SERPINF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1057355 4.40E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_000936 PNLIP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs3010493 3.81E-05 NBL-GWAS version 2 dbGaP|2895
NM_000937 POLR2A 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Sex Hormone-Binding Globulin rs6761 3.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_000944 PPP3CA 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Piperazines rs1405687 5.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_000948 PRL 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs1341239 4.00E-06 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_000948 PRL 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs4236016 4.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_000949 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286411 2.12E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_000949 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 5.38E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_000949 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 6.67E-07 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_000949 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs169587 1.61E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_000949 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1605683 1.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_000949 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286388 1.39E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_000949 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 1.29E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_000949 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 3.17E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_000958 PTGER4 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs2548145 2.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_000958 PTGER4 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs4613763 7.00E-27 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_000958 PTGER4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4613763 6.97E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_000958 PTGER4 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs17234657 2.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_000958 PTGER4 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs11742570 7.00E-36 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_000958 PTGER4 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6451493 3.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_000958 PTGER4 17684544 http://www.ncbi.nlm.nih.gov/pubmed/17684544 Crohn Disease rs1992660 4.00E-07 Systematic association mapping identifies NELL1 as a novel IBD disease gene. NHGRI|-1
NM_000958 PTGER4 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs6896969 2.00E-07 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_000958 PTGER4 17447842 http://www.ncbi.nlm.nih.gov/pubmed/17447842 Crohn Disease rs1373692 2.00E-12 Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4. NHGRI|-1
NM_000958 PTGER4 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs9292777 3.00E-18 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_000958 PTGER4 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs10440635 3.00E-07 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_000963 PTGS2 18471798 http://www.ncbi.nlm.nih.gov/pubmed/18471798 "Osteoarthritis, Knee" rs4140564 3.00E-06 Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis. NHGRI|-1
NM_000963 PTGS2 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs10911902 2.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_000965 RARB 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs1435703 4.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_000965 RARB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6795607 2.36E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000965 RARB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9819865 6.81E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_000965 RARB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10865802 1.32E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_000965 RARB 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs993804 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_000965 RARB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs993804 4.39E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_000967 RPL3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs2413583 1.00E-26 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_000967 RPL3 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs968451 1.00E-09 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_000967 RPL3 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs54211 8.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_000969 RPL5 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs6604026 3.00E-06 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_000969 RPL5 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6604026 8.00E-06 Risk alleles for multiple sclerosis identified by a genomewide study. NHGRI|-1
NM_000969 RPL5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6604026 1.01E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_000969 RPL5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10782945 7.36E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_000999 RPL38 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7219464 1.67E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001001290 SLC2A9 18759275 http://www.ncbi.nlm.nih.gov/pubmed/18759275 Uric Acid rs16890979 1.00E-11 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. NHGRI|-1
NM_001001290 SLC2A9 18834626 http://www.ncbi.nlm.nih.gov/pubmed/18834626 Uric Acid rs16890979 7.00E-168 Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study. NHGRI|-1
NM_001001290 SLC2A9 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs734553 1.00E-192 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_001001290 SLC2A9 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs734553 1.00E-41 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_001001290 SLC2A9 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Gout rs13129697 4.00E-13 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_001001290 SLC2A9 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Uric Acid rs13129697 1.00E-09 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001001290 SLC2A9 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs13129697 2.00E-242 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_001001290 SLC2A9 18327257 http://www.ncbi.nlm.nih.gov/pubmed/18327257 Uric Acid rs737267 3.00E-09 "SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout." NHGRI|-1
NM_001001290 SLC2A9 17997608 http://www.ncbi.nlm.nih.gov/pubmed/17997608 Uric Acid rs6855911 2.00E-16 The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts. NHGRI|-1
NM_001001290 SLC2A9 18179892 http://www.ncbi.nlm.nih.gov/pubmed/18179892 Uric Acid rs7442295 2.00E-15 Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. NHGRI|-1
NM_001001290 SLC2A9 18327256 http://www.ncbi.nlm.nih.gov/pubmed/18327256 Uric Acid rs7442295 3.00E-70 SLC2A9 influences uric acid concentrations with pronounced sex-specific effects. NHGRI|-1
NM_001001290 SLC2A9 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs3775948 1.00E-09 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_001001323 ATP2B1 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs2681472 1.00E-09 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001001323 ATP2B1 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs2681472 2.00E-11 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001001323 ATP2B1 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs2681492 4.00E-11 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001001323 ATP2B1 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Blood Pressure rs17249754 1.00E-07 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001001323 ATP2B1 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs17249754 2.00E-13 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_001001323 ATP2B1 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Blood Pressure rs17249754 3.00E-06 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001001323 ATP2B1 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs17249754 8.00E-20 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_001001330 REEP3 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs2893923 5.00E-08 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001001330 REEP3 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs10761779 7.00E-10 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_001001331 ATP2B2 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Phenylalanine rs6807064 1.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_001001331 ATP2B2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs12632101 2.55E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001001389 CD44 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2295756 9.65E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001001390 CD44 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2295756 9.65E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001001391 CD44 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2295756 9.65E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001001392 CD44 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2295756 9.65E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001001411 ZNF676 20421499 http://www.ncbi.nlm.nih.gov/pubmed/20421499 Telomere rs1975174 2.00E-06 Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. NHGRI|-1
NM_001001415 ZNF429 19207018 http://www.ncbi.nlm.nih.gov/pubmed/19207018 Pain Measurement rs2562456 2.00E-10 Genome-wide association study of acute post-surgical pain in humans. NHGRI|-1
NM_001001484 PTER 19151714 http://www.ncbi.nlm.nih.gov/pubmed/19151714 Obesity rs10508503 2.00E-07 Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. NHGRI|-1
NM_001001547 CD36 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs10499859 3.00E-06 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NM_001001548 CD36 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs10499859 3.00E-06 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NM_001001551 C9orf103 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10868025 1.79E-07 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001001551 C9orf103 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10868025 6.46E-07 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001001657 OR2Y1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs12517906 6.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001001657 OR2Y1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs12517906 7.00E-08 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001001665 CYP27C1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs12989701 3.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_001001665 CYP27C1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs7561528 4.00E-14 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_001001665 CYP27C1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs744373 1.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_001001665 CYP27C1 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs744373 2.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_001001665 CYP27C1 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs744373 3.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_001001671 MAP3K15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs16997315 4.66E-11 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001001694 IL17REL 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs5771069 2.00E-07 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001001694 IL17REL 20228798 http://www.ncbi.nlm.nih.gov/pubmed/20228798 "Colitis, Ulcerative" rs5771069 4.00E-08 Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). NHGRI|-1
NM_001001709 C9orf170 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1923782 8.03E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001001709 C9orf170 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4878061 2.42E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001001709 C9orf170 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs1806864 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001001711 DDI1 20031604 http://www.ncbi.nlm.nih.gov/pubmed/20031604 Matrix Metalloproteinases rs11226373 2.00E-18 Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels. NHGRI|-1
NM_001001715 FARP1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs4318070 7.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001001715 FARP1 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs688872 1.00E-06 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001001715 FARP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs688872 4.44E-04 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_001001715 FARP1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs9584805 2.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001001786 BLID 19779542 http://www.ncbi.nlm.nih.gov/pubmed/19779542 "Myopia, Degenerative" rs577948 2.00E-07 A genome-wide association analysis identified a novel susceptible locus for pathological myopia at 11q24.1. NHGRI|-1
NM_001001786 BLID 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Platelet Aggregation rs565229 4.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001001786 BLID 20838585 http://www.ncbi.nlm.nih.gov/pubmed/20838585 Waist Circumference rs7121446 3.00E-06 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. NHGRI|-1
NM_001001851 ITIH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs4748940 3.09E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001001852 PIM3 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs28372448 8.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_001001872 C14orf37 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2747104 1.26E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001001872 C14orf37 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Bipolar Disorder rs10134944 7.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001001872 C14orf37 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1092015 2.23E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001001872 C14orf37 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs8013190 7.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001001872 C14orf37 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs1335515 8.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_001001872 C14orf37 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Maximal Midexpiratory Flow Rate rs808225 7.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_001001872 C14orf37 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2747100 1.13E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001001888 VCX3B 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs7892812 8.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001001890 RUNX1 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs2014300 8.00E-22 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001001894 TTC3 20463881 http://www.ncbi.nlm.nih.gov/pubmed/20463881 Eye Color rs1003719 2.00E-10 Digital quantification of human eye color highlights genetic association of three new loci. NHGRI|-1
NM_001001895 UBASH3A 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs11203203 4.00E-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001001895 UBASH3A 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs11203203 1.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_001001895 UBASH3A 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs11203203 2.00E-09 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001001895 UBASH3A 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs11203203 1.00E-09 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_001001895 UBASH3A 18840781 http://www.ncbi.nlm.nih.gov/pubmed/18840781 "Diabetes Mellitus, Type 1" rs9976767 2.00E-08 Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes. NHGRI|-1
NM_001001918 OR14C36 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair rs4481887 7.00E-24 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001001919 OR13C4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10761033 5.99E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001001919 OR13C4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1523670 6.70E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001001919 OR13C4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1464666 7.04E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001001957 OR2W3 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs11204538 2.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001001961 OR13C3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10761033 5.99E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001001961 OR13C3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1523670 6.70E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001001961 OR13C3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1464666 7.04E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001001971 FAM13C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10509101 3.95E-05 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751890 1.61E-15 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751890 2.15E-16 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001001974 PLEKHA1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs6585827 2.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6585827 1.12E-21 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6585827 1.42E-23 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2280141 1.06E-21 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2280141 1.37E-23 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2292627 2.68E-17 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2292627 4.68E-18 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1882907 4.02E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1882907 6.27E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7091160 1.81E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6585818 1.92E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11598094 2.21E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11598094 5.64E-07 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7080960 4.24E-11 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7080960 5.76E-12 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11200583 5.76E-16 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11200583 8.67E-16 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751889 1.73E-14 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001001974 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751889 2.26E-15 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001001976 ATE1 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs10510102 2.00E-06 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_001002006 NT5C1B 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognition rs1876040 6.00E-08 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001002031 ATP5G2 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs11170631 9.00E-07 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001002231 KLK2 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs2735839 2.00E-18 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_001002257 LCLAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs829642 4.80E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001002257 LCLAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs829646 6.34E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001002265 8-Mar 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs2279434 4.00E-12 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001002265 8-Mar 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs11239550 1.00E-10 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001002266 8-Mar 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs2279434 4.00E-12 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001002266 8-Mar 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs11239550 1.00E-10 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001002292 WLS 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs187922 2.61E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001002292 WLS 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1430742 3.00E-13 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001002292 WLS 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2566755 2.00E-12 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001002295 GATA3 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs10508343 8.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001002796 MCTP1 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs17418283 1.00E-07 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001002843 ZNF280D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7175191 1.64E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001002901 FCRLB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1027702 2.71E-07 NBL-GWAS version 2 dbGaP|2895
NM_001002911 GPR139 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6497465 5.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001002911 GPR139 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs8054898 5.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001002911 GPR139 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs12444979 3.00E-21 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001002919 FAM150B 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1316288 1.03E-04 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001002919 FAM150B 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs2947411 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001002919 FAM150B 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2867125 3.00E-49 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001002919 FAM150B 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs6548238 1.00E-18 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_001002919 FAM150B 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs7561317 4.00E-17 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001002919 FAM150B 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7561317 2.00E-18 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001002926 TWISTNB 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2192476 4.92E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001003 RPLP1 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs17374222 2.00E-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001003 RPLP1 17903304 http://www.ncbi.nlm.nih.gov/pubmed/17903304 Atrial Fibrillation rs4776472 8.00E-06 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. NHGRI|-1
NM_001003 RPLP1 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs7176508 5.00E-12 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NM_001003398 BICD1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs10844154 4.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001003398 BICD1 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs10844154 6.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_001003398 BICD1 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs708224 3.00E-07 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_001003398 BICD1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs261902 4.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001003674 C18orf1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6505798 8.21E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001003675 C18orf1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6505798 8.21E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001003676 C11orf49 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs7117404 9.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001003677 C11orf49 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs7117404 9.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001003678 C11orf49 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs7117404 9.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001003679 LEPR 20167575 http://www.ncbi.nlm.nih.gov/pubmed/20167575 "Receptors, Leptin" rs1751492 6.00E-13 Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels. NHGRI|-1
NM_001003679 LEPR 19567438 http://www.ncbi.nlm.nih.gov/pubmed/19567438 C-Reactive Protein rs6700896 3.00E-14 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. NHGRI|-1
NM_001003680 LEPR 20167575 http://www.ncbi.nlm.nih.gov/pubmed/20167575 "Receptors, Leptin" rs1751492 6.00E-13 Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels. NHGRI|-1
NM_001003680 LEPR 19567438 http://www.ncbi.nlm.nih.gov/pubmed/19567438 C-Reactive Protein rs6700896 3.00E-14 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. NHGRI|-1
NM_001003681 HMGXB4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2092331 2.28E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001003688 SMAD1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs568752 1.70E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001003693 LY6G6F 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2242653 1.63E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001003693 LY6G6F 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2242653 3.23E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001003698 RREB1 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs11755724 1.00E-06 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_001003698 RREB1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs557074 4.36E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001003698 RREB1 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs675209 1.00E-09 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_001003699 RREB1 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs11755724 1.00E-06 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_001003699 RREB1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs557074 4.36E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001003699 RREB1 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs675209 1.00E-09 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_001003700 RREB1 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs11755724 1.00E-06 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_001003700 RREB1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs557074 4.36E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001003700 RREB1 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs675209 1.00E-09 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_001003792 RBMS3 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs1530057 3.00E-06 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_001003792 RBMS3 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Bone Density rs10510628 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001003792 RBMS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6778464 1.22E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001003792 RBMS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9877517 6.53E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001003793 RBMS3 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs1530057 3.00E-06 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_001003793 RBMS3 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Bone Density rs10510628 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001003793 RBMS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6778464 1.22E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001003793 RBMS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9877517 6.53E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001003809 DLGAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs3915772 8.43E-05 NBL-GWAS version 2 dbGaP|2895
NM_001003809 DLGAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs431220 5.88E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001003845 SP5 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs2080401 7.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001003892 DUPD1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs7919006 4.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001003892 DUPD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7896442 2.45E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001003892 DUPD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7896442 7.84E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001003931 PARP3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs929533 3.79E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001003940 BMF 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs7181230 5.00E-11 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001003942 BMF 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs7181230 5.00E-11 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001003943 BMF 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs7181230 5.00E-11 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001003954 ANXA13 21046636 http://www.ncbi.nlm.nih.gov/pubmed/21046636 Brain Waves rs2294015 9.00E-06 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. NHGRI|-1
NM_001003954 ANXA13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs2294015 5.83E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_001003954 ANXA13 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs10088262 4.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_001004019 FBLN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17793957 1.85E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001004019 FBLN2 21368711 http://www.ncbi.nlm.nih.gov/pubmed/21368711 Personality rs9846232 1.00E-08 Genome-wide association study of personality traits in bipolar patients. NHGRI|-1
NM_001004052 OR52B2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs325648 7.23E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001004065 AKAP2 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs7032940 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001004105 GRK6 21546496 http://www.ncbi.nlm.nih.gov/pubmed/21546496 Blood Platelets rs2731672 1.00E-06 Novel loci involved on platelet function and platelet count identified by a genome-wide study performed in children. NHGRI|-1
NM_001004105 GRK6 20303064 http://www.ncbi.nlm.nih.gov/pubmed/20303064 Partial Thromboplastin Time rs2731672 2.00E-30 "Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time." NHGRI|-1
NM_001004106 GRK6 21546496 http://www.ncbi.nlm.nih.gov/pubmed/21546496 Blood Platelets rs2731672 1.00E-06 Novel loci involved on platelet function and platelet count identified by a genome-wide study performed in children. NHGRI|-1
NM_001004106 GRK6 20303064 http://www.ncbi.nlm.nih.gov/pubmed/20303064 Partial Thromboplastin Time rs2731672 2.00E-30 "Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time." NHGRI|-1
NM_001004125 TUSC1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10453196 3.37E-06 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001004125 TUSC1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10491819 5.58E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001004125 TUSC1 19483685 http://www.ncbi.nlm.nih.gov/pubmed/19483685 Drug-Induced Liver Injury rs10812428 1.00E-06 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. NHGRI|-1
NM_001004125 TUSC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12236180 4.63E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001004125 TUSC1 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs1889899 6.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001004125 TUSC1 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs4246856 6.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001004125 TUSC1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Weight rs2225614 3.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001004125 TUSC1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10491833 5.28E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001004125 TUSC1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9406815 9.13E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001004125 TUSC1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs12552736 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001004125 TUSC1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs13300284 4.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001004125 TUSC1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs17774966 8.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001004298 C10orf90 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4255455 6.99E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001004303 C1orf168 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs10489622 2.45E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001004308 ZCCHC16 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Triglycerides rs5982533 7.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001004316 LEKR1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs12638253 2.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001004316 LEKR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12638253 8.31E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001004316 LEKR1 20372150 http://www.ncbi.nlm.nih.gov/pubmed/20372150 Birth Weight rs900400 2.00E-35 Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. NHGRI|-1
NM_001004316 LEKR1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs13064954 7.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001004317 LIN28B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs17065417 6.85E-05 NBL-GWAS version 2 dbGaP|2895
NM_001004317 LIN28B 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs314277 1.00E-08 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001004317 LIN28B 20303062 http://www.ncbi.nlm.nih.gov/pubmed/20303062 Body Height rs314277 2.00E-06 "A variant in LIN28B is associated with 2D:4D finger-length ratio, a putative retrospective biomarker of prenatal testosterone exposure." NHGRI|-1
NM_001004317 LIN28B 19448621 http://www.ncbi.nlm.nih.gov/pubmed/19448621 Menarche rs314277 3.00E-13 Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. NHGRI|-1
NM_001004317 LIN28B 19448623 http://www.ncbi.nlm.nih.gov/pubmed/19448623 Menarche rs314276 4.00E-16 Genetic variation in LIN28B is associated with the timing of puberty. NHGRI|-1
NM_001004317 LIN28B 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs314268 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001004317 LIN28B 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7759938 5.00E-60 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001004317 LIN28B 19448620 http://www.ncbi.nlm.nih.gov/pubmed/19448620 Menarche rs7759938 7.00E-09 Meta-analysis of genome-wide association data identifies two loci influencing age at menarche. NHGRI|-1
NM_001004317 LIN28B 19448622 http://www.ncbi.nlm.nih.gov/pubmed/19448622 Menarche rs314280 2.00E-14 Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche. NHGRI|-1
NM_001004318 PAPL 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs472265 9.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_001004318 PAPL 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs930100 2.15E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001004320 TMEM195 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6977610 1.72E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001004320 TMEM195 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7788248 4.96E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001004320 TMEM195 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs10244051 1.45E-07 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_001004320 TMEM195 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Glucose rs10244051 1.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001004320 TMEM195 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs2191349 3.00E-44 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001004320 TMEM195 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs2191349 3.00E-17 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001004342 TRIM67 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4388693 3.06E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001004356 FGFRL1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6839931 2.09E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001004356 FGFRL1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7669622 4.53E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001004356 FGFRL1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6827357 5.15E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001004358 FGFRL1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6839931 2.09E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001004358 FGFRL1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7669622 4.53E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001004358 FGFRL1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6827357 5.15E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001004360 DPP10 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4624391 9.77E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001004360 DPP10 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4277531 9.40E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001004419 CLEC2D 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs3764021 5.00E-08 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001004426 PLA2G6 19578365 http://www.ncbi.nlm.nih.gov/pubmed/19578365 Dysplastic Nevus Syndrome rs2284063 3.00E-08 Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. NHGRI|-1
NM_001004426 PLA2G6 19578364 http://www.ncbi.nlm.nih.gov/pubmed/19578364 Melanoma rs2284063 2.00E-09 Genome-wide association study identifies three loci associated with melanoma risk. NHGRI|-1
NM_001004426 PLA2G6 21478494 http://www.ncbi.nlm.nih.gov/pubmed/21478494 Cutaneous nevi rs738322 1.00E-06 Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk. NHGRI|-1
NM_001004439 ITGA11 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs7164335 1.00E-07 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_001004439 ITGA11 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs1445021 9.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001004439 ITGA11 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs11856323 1.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001004440 FAM19A3 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs11590090 3.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001004454 OR1L8 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10818721 5.85E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001004469 OR10J5 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Hemoglobins rs4133289 2.00E-07 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001004470 ST8SIA6 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs359312 9.00E-08 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001004490 OR2AG2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs951340 2.20E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001004691 OR2M7 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair rs4481887 7.00E-24 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001004760 OR51V1 19465909 http://www.ncbi.nlm.nih.gov/pubmed/19465909 Malaria rs11036238 4.00E-11 Genome-wide and fine-resolution association analysis of malaria in West Africa. NHGRI|-1
NM_001005158 SFMBT1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2336725 1.00E-12 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001005159 SFMBT1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2336725 1.00E-12 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001005176 SP140 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs13397985 6.00E-10 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NM_001005176 SP140 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs7423615 3.00E-13 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001005178 OR52W1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs325648 7.23E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001005188 OR6X1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10893085 9.84E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001005188 OR6X1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11219274 8.17E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001005194 OR8A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs12792184 7.08E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001005195 OR8B12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs948725 2.04E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001005207 TRIM37 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs3809724 9.48E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001005213 OR9G1 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Indices rs1397048 7.00E-08 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001005213 OR9G9 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1912373 5.30E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001005213 OR9G9 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1912373 6.33E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001005216 OR2J3 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs3129109 2.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001005275 OR4A15 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs7927370 7.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_001005285 OR2AT4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4435030 6.88E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001005290 PSRC1 20442857 http://www.ncbi.nlm.nih.gov/pubmed/20442857 1-Alkyl-2-acetylglycerophosphocholine Esterase rs599839 3.00E-15 Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study. NHGRI|-1
NM_001005290 PSRC1 18262040 http://www.ncbi.nlm.nih.gov/pubmed/18262040 "Cholesterol, LDL" rs599839 1.00E-33 LDL-cholesterol concentrations: a genome-wide association study. NHGRI|-1
NM_001005290 PSRC1 18179892 http://www.ncbi.nlm.nih.gov/pubmed/18179892 "Cholesterol, LDL" rs599839 1.00E-07 Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. NHGRI|-1
NM_001005290 PSRC1 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs599839 6.00E-33 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001005290 PSRC1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs599839 3.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001005290 PSRC1 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs599839 4.00E-09 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_001005291 SREBF1 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs11868035 6.00E-08 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_001005336 DNM1 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2502731 2.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_001005337 PKP1 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs860554 5.00E-08 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_001005337 PKP1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs832147 6.81E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001005339 RGS10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10886492 7.15E-05 NBL-GWAS version 2 dbGaP|2895
NM_001005339 RGS10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2991769 3.09E-05 NBL-GWAS version 2 dbGaP|2895
NM_001005339 RGS10 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2991769 7.72E-07 NBL-GWAS version 1 dbGaP|2845
NM_001005339 RGS10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2991770 1.76E-05 NBL-GWAS version 2 dbGaP|2895
NM_001005339 RGS10 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2991770 8.71E-07 NBL-GWAS version 1 dbGaP|2845
NM_001005360 DNM2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11671653 9.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001005361 DNM2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11671653 9.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001005362 DNM2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11671653 9.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001005413 ZWINT 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs4462262 9.00E-08 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_001005413 ZWINT 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs35866326 4.02E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001005413 ZWINT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11005196 3.65E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001005413 ZWINT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11005240 4.15E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001005470 OR4B1 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs11039571 9.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001005474 NFKBIZ 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs17842780 1.05E-06 NBL-GWAS version 1 dbGaP|2845
NM_001005474 NFKBIZ 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs991258 5.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001005517 OR5K4 19483685 http://www.ncbi.nlm.nih.gov/pubmed/19483685 Drug-Induced Liver Injury rs1497546 2.00E-07 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. NHGRI|-1
NM_001005609 EDA 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs5936487 6.00E-11 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001005609 EDA 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs4844096 5.00E-11 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001005610 EDA 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs5936487 6.00E-11 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001005610 EDA 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs4844096 5.00E-11 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001005612 EDA 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs5936487 6.00E-11 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001005612 EDA 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs4844096 5.00E-11 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001005613 EDA 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs5936487 6.00E-11 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001005613 EDA 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs4844096 5.00E-11 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001005735 CHEK2 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1547014 1.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_001005735 CHEK2 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs738722 1.00E-08 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001005743 NUMB 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Atherosclerosis rs10483853 6.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001005744 NUMB 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Atherosclerosis rs10483853 6.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001005745 NUMB 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Atherosclerosis rs10483853 6.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001005783 HAO2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs868675 6.28E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_001005783 HAO2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1341797 6.95E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001005915 ERBB3 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs2292239 2.00E-20 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_001005915 ERBB3 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2292239 2.00E-25 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001005915 ERBB3 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs2292239 3.00E-16 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_001005915 ERBB3 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs12580100 1.00E-06 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_001005915 ERBB3 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs11171739 1.00E-11 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7514280 9.85E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10874746 3.17E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2811600 1.59E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2811593 2.91E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs35183060 5.50E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7536563 2.24E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2255723 1.94E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12066638 3.64E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11164835 1.46E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs9651257 4.49E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006605 FAM69A 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs12745968 8.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12745968 1.04E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006605 FAM69A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4847386 7.91E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10874753 4.57E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs660870 3.16E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006605 FAM69A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs521428 4.57E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001006638 RAB37 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs10512597 8.00E-11 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_001006655 FAM149A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2276919 4.19E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001006658 CR2 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs17045328 7.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_001006939 LRRC18 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs1913517 7.00E-12 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_001006944 RPS6KA4 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs538147 2.00E-10 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001006945 C1orf103 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1282020 8.95E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001006945 C1orf103 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1282023 8.95E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001006945 C1orf103 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1548342 8.72E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001007090 C8orf48 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11785331 2.85E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001007097 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1034042 1.58E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001007097 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769612 1.60E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001007097 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769605 9.38E-06 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001007097 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769600 1.35E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001007097 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769595 1.17E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001007097 NTRK2 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs2841498 4.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_001007102 L3MBTL3 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs6569648 1.00E-21 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001007102 L3MBTL3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs6899976 6.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001007139 IGF2 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs3741208 2.00E-07 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_001007139 IGF2 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 "Diabetes Mellitus, Type 1" rs1004446 4.00E-09 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NM_001007156 NTRK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs894290 3.03E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001007169 ZNF483 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs10980926 4.00E-11 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001007188 DEPDC5 21725309 http://www.ncbi.nlm.nih.gov/pubmed/21725309 "Hepatitis C, Chronic" rs1012068 1.00E-13 Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers. NHGRI|-1
NM_001007189 C5orf53 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4913069 9.52E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001007225 IGF2BP2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs4402960 1.00E-06 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001007225 IGF2BP2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs4402960 2.00E-09 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001007225 IGF2BP2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs4402960 8.00E-08 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001007225 IGF2BP2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs4402960 9.00E-16 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001007225 IGF2BP2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs4402960 9.00E-16 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001007225 IGF2BP2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs1470579 2.00E-09 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001007225 IGF2BP2 18711366 http://www.ncbi.nlm.nih.gov/pubmed/18711366 "Diabetes Mellitus, Type 2" rs6769511 1.00E-09 SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations. NHGRI|-1
NM_001007225 IGF2BP2 21573907 http://www.ncbi.nlm.nih.gov/pubmed/21573907 "Diabetes Mellitus, Type 2" rs1374910 1.00E-07 "Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas." NHGRI|-1
NM_001007231 ARHGAP25 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs10496166 4.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001007240 GP2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs12444268 2.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001007240 GP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6497465 5.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001007240 GP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs8054898 5.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001007241 GP2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs12444268 2.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001007241 GP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6497465 5.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001007241 GP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs8054898 5.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001007242 GP2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs12444268 2.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001007242 GP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6497465 5.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001007242 GP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs8054898 5.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001007245 IFRD1 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs17159640 9.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_001007257 PRDM2 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs2245218 2.13E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001007267 PLA2R1 21323541 http://www.ncbi.nlm.nih.gov/pubmed/21323541 "Glomerulonephritis, Membranous" rs4664308 9.00E-29 Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy. NHGRI|-1
NM_001007466 TULP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs705936 4.15E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001007466 TULP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6920842 3.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001007470 TRPM3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4745062 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001007470 TRPM3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12350232 8.34E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001007471 TRPM3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4745062 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001007471 TRPM3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12350232 8.34E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001007527 LMBRD2 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs267759 7.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001007537 C1QTNF9B 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs2765086 6.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001007538 SHISA2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs9512144 6.15E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001007559 SS18 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs1840440 3.00E-07 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001007595 C2CD4B 20818381 http://www.ncbi.nlm.nih.gov/pubmed/20818381 "Diabetes Mellitus, Type 2" rs7172432 9.00E-14 A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B. NHGRI|-1
NM_001007595 C2CD4B 20862305 http://www.ncbi.nlm.nih.gov/pubmed/20862305 "Diabetes Mellitus, Type 2" rs1436955 7.00E-07 Identification of new genetic risk variants for type 2 diabetes. NHGRI|-1
NM_001007595 C2CD4B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs6494311 2.18E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001007595 C2CD4B 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs11071657 4.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001008211 OPTN 20436471 http://www.ncbi.nlm.nih.gov/pubmed/20436471 Osteitis Deformans rs1561570 6.00E-13 "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone." NHGRI|-1
NM_001008211 OPTN 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs1561570 4.00E-38 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_001008211 OPTN 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs525455 7.00E-07 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001008212 OPTN 20436471 http://www.ncbi.nlm.nih.gov/pubmed/20436471 Osteitis Deformans rs1561570 6.00E-13 "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone." NHGRI|-1
NM_001008212 OPTN 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs1561570 4.00E-38 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_001008212 OPTN 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs525455 7.00E-07 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001008213 OPTN 20436471 http://www.ncbi.nlm.nih.gov/pubmed/20436471 Osteitis Deformans rs1561570 6.00E-13 "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone." NHGRI|-1
NM_001008213 OPTN 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs1561570 4.00E-38 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_001008213 OPTN 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs525455 7.00E-07 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001008224 UACA 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs6494849 7.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001008228 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3135050 2.42E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001008228 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071653 2.34E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001008228 MOG 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal Neoplasms rs29232 9.00E-17 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_001008228 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3131854 2.54E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001008229 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3135050 2.42E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001008229 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071653 2.34E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001008229 MOG 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal Neoplasms rs29232 9.00E-17 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_001008229 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3131854 2.54E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001008389 UMOD 20686651 http://www.ncbi.nlm.nih.gov/pubmed/20686651 Waist Circumference rs4293393 4.00E-10 Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases. NHGRI|-1
NM_001008389 UMOD 21082022 http://www.ncbi.nlm.nih.gov/pubmed/21082022 Hypertension rs13333226 4.00E-11 Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension. NHGRI|-1
NM_001008389 UMOD 19430482 http://www.ncbi.nlm.nih.gov/pubmed/19430482 Creatinine rs12917707 5.00E-16 Multiple loci associated with indices of renal function and chronic kidney disease. NHGRI|-1
NM_001008389 UMOD 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs12917707 1.00E-20 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001008389 UMOD 19430482 http://www.ncbi.nlm.nih.gov/pubmed/19430482 "Kidney Failure, Chronic" rs12917707 2.00E-12 Multiple loci associated with indices of renal function and chronic kidney disease. NHGRI|-1
NM_001008389 UMOD 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs12444268 2.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001008392 CTDSPL 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Prostatic Neoplasms rs9311171 2.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001008404 C14orf180 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4983568 8.02E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001008405 BCAP29 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs10953541 3.00E-08 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_001008405 BCAP29 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs10953541 9.98E-05 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001008494 ISX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2187961 7.84E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001008494 ISX 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs130575 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001008503 OPRM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs675026 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001008503 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4598087 1.11E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001008503 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754521 9.74E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001008503 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2186140 5.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001008503 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10499276 8.08E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001008504 OPRM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs675026 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001008504 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4598087 1.11E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001008504 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754521 9.74E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001008504 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2186140 5.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001008504 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10499276 8.08E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001008505 OPRM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs675026 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001008505 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4598087 1.11E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001008505 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754521 9.74E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001008505 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2186140 5.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001008505 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10499276 8.08E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001008536 TCHHL1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair rs17646946 2.00E-42 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001008536 TCHHL1 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs3124314 4.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001008539 SLC7A2 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs2720508 7.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001008540 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4954564 5.21E-06 NBL-GWAS version 1 dbGaP|2845
NM_001008540 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1123848 4.90E-06 NBL-GWAS version 1 dbGaP|2845
NM_001008540 CXCR4 17903306 http://www.ncbi.nlm.nih.gov/pubmed/17903306 Electrocardiography rs882300 3.00E-07 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. NHGRI|-1
NM_001008540 CXCR4 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs882300 1.00E-07 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_001008540 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs6430612 4.51E-07 NBL-GWAS version 1 dbGaP|2845
NM_001008540 CXCR4 20421499 http://www.ncbi.nlm.nih.gov/pubmed/20421499 Telomere rs4452212 2.00E-06 Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. NHGRI|-1
NM_001008540 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs309137 3.48E-07 NBL-GWAS version 1 dbGaP|2845
NM_001008540 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs749873 1.79E-06 NBL-GWAS version 1 dbGaP|2845
NM_001008540 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2011946 7.16E-06 NBL-GWAS version 1 dbGaP|2845
NM_001008540 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs932206 1.07E-06 NBL-GWAS version 1 dbGaP|2845
NM_001008541 MXI1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs716595 8.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001008541 MXI1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7917994 8.56E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001008541 MXI1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7921757 8.56E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001008660 PICALM 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs536841 3.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_001008660 PICALM 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs561655 7.00E-11 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_001008660 PICALM 19734902 http://www.ncbi.nlm.nih.gov/pubmed/19734902 Alzheimer Disease rs3851179 1.00E-09 Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. NHGRI|-1
NM_001008693 CST9 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs911119 2.00E-138 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001008693 CST9 17903292 http://www.ncbi.nlm.nih.gov/pubmed/17903292 Cystatin C rs1158167 9.00E-09 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001008701 LPHN1 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs4528684 1.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_001008707 EML1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4905898 5.84E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001008707 EML1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs10141863 3.75E-06 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001008707 EML1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs12891247 6.53E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001008901 GTSF1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11696193 6.20E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001008938 CKAP5 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs1007738 7.00E-07 New sequence variants associated with bone mineral density. NHGRI|-1
NM_001009554 MFAP3L 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4692758 9.61E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001009562 LST-3TM12 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs2117032 3.00E-14 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_001009571 CADPS2 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs2429582 6.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001009811 AZI1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs7225354 9.76E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001009905 B3GNTL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1551628 1.03E-04 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001009905 B3GNTL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1551628 3.29E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001009905 B3GNTL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9901757 3.21E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001009909 LUZP2 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4561213 3.00E-07 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001009909 LUZP2 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs10500991 2.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001009909 LUZP2 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs12794435 5.00E-06 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_001009921 VPS8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10937194 5.90E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001009923 C20orf30 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs261360 3.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001009924 C20orf30 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs261360 3.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001009925 C20orf30 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs261360 3.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001009936 PHF19 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs1953126 4.00E-11 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_001009936 PHF19 19503088 http://www.ncbi.nlm.nih.gov/pubmed/19503088 "Arthritis, Rheumatoid" rs881375 4.00E-08 "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis." NHGRI|-1
NM_001009941 ANKRD16 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2380205 5.00E-07 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001009943 ANKRD16 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2380205 5.00E-07 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001009958 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Anthropometry rs7792939 5.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001009958 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weight rs7792939 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001009958 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weights and Measures rs7792939 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001009960 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Anthropometry rs7792939 5.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001009960 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weight rs7792939 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001009960 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weights and Measures rs7792939 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001009984 C20orf194 21703177 http://www.ncbi.nlm.nih.gov/pubmed/21703177 "Hepatitis C, Chronic" rs965469 1.00E-09 Genome-wide association study of interferon-related cytopenia in chronic hepatitis C patients. NHGRI|-1
NM_001009991 SYTL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9364496 1.79E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001009991 SYTL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6455600 1.19E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001009991 SYTL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2129209 2.62E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001009991 SYTL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9456350 2.32E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001010000 ARHGAP28 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs597503 2.00E-08 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001010000 ARHGAP28 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6506389 5.62E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001010848 NRG3 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs4933824 2.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001010848 NRG3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2250544 9.03E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001010848 NRG3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2494028 5.41E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001010848 NRG3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2249075 1.47E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001010848 NRG3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2820096 1.33E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001010848 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17689242 5.66E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001010848 NRG3 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs2224865 9.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_001010848 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs2224865 9.98E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_001010848 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11200376 6.80E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001010848 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11200394 6.80E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001010848 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12220373 6.80E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001010848 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11200700 1.00E-04 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001010848 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7068193 6.40E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001010848 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4615965 8.65E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001010848 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7906877 8.92E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001010848 NRG3 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1484170 1.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001010848 NRG3 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Nonalcoholic Fatty Liver Disease rs588517 8.00E-06 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_001010853 PM20D2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs10223547 1.93E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001010861 LPPR5 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1351563 7.27E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001010872 FAM83B 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs6911198 3.98E-06 NBL-GWAS version 1 dbGaP|2845
NM_001010874 TECRL 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs13126803 1.20E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001010877 ZNF311 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3130893 9.64E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001010877 ZNF311 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3129791 1.10E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001010891 MTX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7735699 1.78E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001010891 MTX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs265010 2.67E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001010897 SERP2 18759275 http://www.ncbi.nlm.nih.gov/pubmed/18759275 Uric Acid rs17065323 4.00E-06 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. NHGRI|-1
NM_001010904 GLYATL3 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs9473582 8.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001010906 C8orf80 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs4732812 3.00E-06 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9295938 9.16E-18 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs886403 5.60E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1634718 2.64E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs13191258 3.95E-33 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113313862 8.09E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9366764 8.10E-18 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3871466 3.74E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3871466 7.90E-17 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9262492 2.99E-11 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2894176 9.71E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9394031 8.25E-18 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112511267 1.97E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs17190071 1.55E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2517552 8.16E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs80077509 3.09E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2523870 2.73E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2844645 7.29E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2251830 2.52E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2523864 1.96E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2517527 1.83E-11 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844697 6.16E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3095089 1.03E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3095089 2.09E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001010909 MUC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844680 6.06E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001010927 TIAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7741028 7.77E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001010927 TIAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9384296 1.71E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001010927 TIAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12528887 1.25E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001010927 TIAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12523857 1.25E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001010931 HGF 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs4236644 2.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_001010932 HGF 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs4236644 2.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_001010933 HGF 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs4236644 2.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_001010934 HGF 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs4236644 2.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_001010935 RAP1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10857899 3.06E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001010935 RAP1A 20548944 http://www.ncbi.nlm.nih.gov/pubmed/20548944 Bone Density rs494453 4.00E-08 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. NHGRI|-1
NM_001010942 RAP1B 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs12313946 3.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001010971 SAMD13 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs1085093 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001010989 HERPUD1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs2217332 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001010989 HERPUD1 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs9989419 3.00E-31 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001010989 HERPUD1 20031538 http://www.ncbi.nlm.nih.gov/pubmed/20031538 "Cholesterol, HDL" rs9989419 9.00E-27 Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions. NHGRI|-1
NM_001010989 HERPUD1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs9989419 1.00E-32 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001010989 HERPUD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs9989419 2.21E-09 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_001010989 HERPUD1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs173539 4.00E-75 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001010989 HERPUD1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs173539 5.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001010989 HERPUD1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs173539 1.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001010989 HERPUD1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs173539 9.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001010989 HERPUD1 20838585 http://www.ncbi.nlm.nih.gov/pubmed/20838585 Cardiovascular Diseases rs247616 1.00E-23 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. NHGRI|-1
NM_001010989 HERPUD1 18454146 http://www.ncbi.nlm.nih.gov/pubmed/18454146 "Cholesterol, HDL" rs3764261 1.00E-27 Common genetic variation near MC4R is associated with waist circumference and insulin resistance. NHGRI|-1
NM_001010989 HERPUD1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs3764261 1.00E-48 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001010989 HERPUD1 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs3764261 2.00E-57 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001010989 HERPUD1 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, HDL" rs3764261 7.00E-29 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001010989 HERPUD1 19359809 http://www.ncbi.nlm.nih.gov/pubmed/19359809 "Cholesterol, LDL" rs3764261 3.00E-12 Identification of genetic markers associated with high-density lipoprotein-cholesterol by genome-wide screening in a Japanese population: the Suita study. NHGRI|-1
NM_001010989 HERPUD1 20686565 http://www.ncbi.nlm.nih.gov/pubmed/20686565 Lipids rs3764261 7E-380 "Biological, clinical and population relevance of 95 loci for blood lipids." NHGRI|-1
NM_001010989 HERPUD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs3764261 6.97E-29 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_001010989 HERPUD1 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs3764261 7.00E-07 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_001010989 HERPUD1 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs3764261 7.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001010989 HERPUD1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs3764261 3.00E-13 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001010990 HERPUD1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs2217332 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001010990 HERPUD1 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs9989419 3.00E-31 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001010990 HERPUD1 20031538 http://www.ncbi.nlm.nih.gov/pubmed/20031538 "Cholesterol, HDL" rs9989419 9.00E-27 Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions. NHGRI|-1
NM_001010990 HERPUD1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs9989419 1.00E-32 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001010990 HERPUD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs9989419 2.21E-09 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_001010990 HERPUD1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs173539 4.00E-75 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001010990 HERPUD1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs173539 5.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001010990 HERPUD1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs173539 1.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001010990 HERPUD1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs173539 9.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001010990 HERPUD1 20838585 http://www.ncbi.nlm.nih.gov/pubmed/20838585 Cardiovascular Diseases rs247616 1.00E-23 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. NHGRI|-1
NM_001010990 HERPUD1 18454146 http://www.ncbi.nlm.nih.gov/pubmed/18454146 "Cholesterol, HDL" rs3764261 1.00E-27 Common genetic variation near MC4R is associated with waist circumference and insulin resistance. NHGRI|-1
NM_001010990 HERPUD1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs3764261 1.00E-48 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001010990 HERPUD1 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs3764261 2.00E-57 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001010990 HERPUD1 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, HDL" rs3764261 7.00E-29 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001010990 HERPUD1 19359809 http://www.ncbi.nlm.nih.gov/pubmed/19359809 "Cholesterol, LDL" rs3764261 3.00E-12 Identification of genetic markers associated with high-density lipoprotein-cholesterol by genome-wide screening in a Japanese population: the Suita study. NHGRI|-1
NM_001010990 HERPUD1 20686565 http://www.ncbi.nlm.nih.gov/pubmed/20686565 Lipids rs3764261 7E-380 "Biological, clinical and population relevance of 95 loci for blood lipids." NHGRI|-1
NM_001010990 HERPUD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs3764261 6.97E-29 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_001010990 HERPUD1 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs3764261 7.00E-07 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_001010990 HERPUD1 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs3764261 7.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001010990 HERPUD1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs3764261 3.00E-13 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001011513 PDLIM5 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs12500426 1.00E-11 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001011513 PDLIM5 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs17021918 4.00E-15 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001011515 PDLIM5 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs12500426 1.00E-11 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001011515 PDLIM5 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs17021918 4.00E-15 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001011516 PDLIM5 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs12500426 1.00E-11 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001011516 PDLIM5 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs17021918 4.00E-15 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001011552 SLC9A4 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Eosinophils rs17027258 7.00E-06 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001011552 SLC9A4 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs917997 1.00E-15 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001011645 AR 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs5031002 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001011645 AR 18849991 http://www.ncbi.nlm.nih.gov/pubmed/18849991 Alopecia rs6625163 5.00E-11 Male-pattern baldness susceptibility locus at 20p11. NHGRI|-1
NM_001011649 CDK5RAP2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4642724 3.93E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001011649 CDK5RAP2 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs16909449 1.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001011649 CDK5RAP2 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Cornea rs4837752 6.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_001011655 TMEM44 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs789852 7.00E-07 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001011666 CREB5 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs11765845 7.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001011666 CREB5 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2237349 5.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_001011667 CHCHD7 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs9650315 4.00E-07 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001011667 CHCHD7 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs7815788 5.00E-06 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001011668 CHCHD7 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs9650315 4.00E-07 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001011668 CHCHD7 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs7815788 5.00E-06 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001011669 CHCHD7 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs9650315 4.00E-07 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001011669 CHCHD7 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs7815788 5.00E-06 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001011670 CHCHD7 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs9650315 4.00E-07 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001011670 CHCHD7 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs7815788 5.00E-06 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001011671 CHCHD7 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs9650315 4.00E-07 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001011671 CHCHD7 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs7815788 5.00E-06 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001011700 MCCD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113945015 6.93E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001011700 MCCD1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3115537 2.46E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001011700 MCCD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3093978 8.82E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001011703 FAM125B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs888219 2.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001011708 OLA1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11688834 1.04E-04 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001011713 NAA30 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11620639 1.59E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001011880 CLEC18B 18463975 http://www.ncbi.nlm.nih.gov/pubmed/18463975 Breast Neoplasms rs10871290 4.00E-07 A pilot genome-wide association study of early-onset breast cancer. NHGRI|-1
NM_001011885 BTBD1 21326860 http://www.ncbi.nlm.nih.gov/pubmed/21326860 Mucocutaneous Lymph Node Syndrome rs1568657 7.00E-06 Identification of novel susceptibility Loci for kawasaki disease in a han chinese population by a genome-wide association study. NHGRI|-1
NM_001012338 NTRK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs894290 3.03E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001012393 OPCML 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7125438 2.08E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001012393 OPCML 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs4397868 3.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_001012409 SGOL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6776153 9.43E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001012409 SGOL1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs11720452 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001012409 SGOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1395993 3.49E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001012410 SGOL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6776153 9.43E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001012410 SGOL1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs11720452 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001012410 SGOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1395993 3.49E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001012411 SGOL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6776153 9.43E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001012411 SGOL1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs11720452 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001012411 SGOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1395993 3.49E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001012412 SGOL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6776153 9.43E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001012412 SGOL1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs11720452 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001012412 SGOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1395993 3.49E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001012413 SGOL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6776153 9.43E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001012413 SGOL1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs11720452 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001012413 SGOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1395993 3.49E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001012426 FOXP4 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs1983891 8.00E-08 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_001012427 FOXP4 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs1983891 8.00E-08 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_001012456 SEC61G 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs2252586 8.00E-08 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_001012505 FOXP1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs17651978 6.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001012505 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9819066 4.55E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001012505 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9828629 8.89E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001012505 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6549392 2.33E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001012505 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11720523 2.09E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001012505 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6779258 1.11E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001012505 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11720121 1.28E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001012505 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6549400 8.46E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001012505 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10460943 7.33E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001012505 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1090502 8.12E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001012505 FOXP1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Mass Index rs1024889 6.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001012506 CCDC66 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs2054989 6.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001012507 CENPW 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs9388489 4.00E-13 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001012507 CENPW 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1361108 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001012507 CENPW 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1490388 6.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001012507 CENPW 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs4549631 5.00E-13 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001012509 SLC45A2 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs16891982 1.00E-12 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001012509 SLC45A2 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs16891982 4.00E-20 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001012509 SLC45A2 17999355 http://www.ncbi.nlm.nih.gov/pubmed/17999355 Skin Pigmentation rs16891982 3.00E-11 A genomewide association study of skin pigmentation in a South Asian population. NHGRI|-1
NM_001012509 SLC45A2 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs35391 3.00E-10 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_001012509 SLC45A2 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs28777 1.00E-17 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_001012509 SLC45A2 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs28777 9.00E-14 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_001012511 GOSR2 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs17608766 5.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001012512 GRP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9961404 1.02E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001012512 GRP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1517037 6.81E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001012512 GRP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9319943 3.34E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001012513 GRP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9961404 1.02E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001012513 GRP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1517037 6.81E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001012513 GRP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9319943 3.34E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001012706 C14orf182 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs8013833 6.01E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001012957 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001012957 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001012957 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001012957 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001012958 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001012958 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001012958 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001012958 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001012959 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001012959 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001012959 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001012959 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001012967 DDX60L 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs2710833 6.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001012975 RNASE10 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Nonalcoholic Fatty Liver Disease rs12147450 6.00E-07 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_001012980 SATL1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2285602 2.37E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001012980 SATL1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2188734 4.65E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001012993 C9orf152 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs7032940 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001013031 SORCS1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2245437 6.05E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001013031 SORCS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1931605 1.68E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001013031 SORCS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11592212 5.16E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001013253 LSP1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs907611 1.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001013253 LSP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11041553 2.86E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001013253 LSP1 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs3817198 3.00E-09 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_001013254 LSP1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs907611 1.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001013254 LSP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11041553 2.86E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001013254 LSP1 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs3817198 3.00E-09 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_001013255 LSP1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs907611 1.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001013255 LSP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11041553 2.86E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001013255 LSP1 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs3817198 3.00E-09 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_001013358 OR9G1 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Indices rs1397048 7.00E-08 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001013358 OR9G9 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1912373 5.30E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001013358 OR9G9 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1912373 6.33E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001013398 IGFBP3 21216879 http://www.ncbi.nlm.nih.gov/pubmed/21216879 Insulin-Like Growth Factor Binding Protein 3 rs11977526 3.00E-101 A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. NHGRI|-1
NM_001013403 CXorf66 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs5907577 3.65E-06 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001013403 CXorf66 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4825220 2.01E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001013403 CXorf66 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs677033 2.31E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001013403 CXorf66 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs613278 1.03E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001013403 CXorf66 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs5955415 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001013403 CXorf66 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs5955415 3.99E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001013415 FBXW7 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs360929 9.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_001013442 EPGN 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1350666 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001013619 AGPHD1 18780872 http://www.ncbi.nlm.nih.gov/pubmed/18780872 Lung Neoplasms rs8034191 1.00E-08 Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer. NHGRI|-1
NM_001013619 AGPHD1 18385676 http://www.ncbi.nlm.nih.gov/pubmed/18385676 Lung Neoplasms rs8034191 3.00E-18 Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. NHGRI|-1
NM_001013619 AGPHD1 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs8034191 3.00E-26 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_001013619 AGPHD1 18385738 http://www.ncbi.nlm.nih.gov/pubmed/18385738 Lung Neoplasms rs8034191 5.00E-20 A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. NHGRI|-1
NM_001013619 AGPHD1 19300482 http://www.ncbi.nlm.nih.gov/pubmed/19300482 "Pulmonary Disease, Chronic Obstructive" rs8034191 1.00E-10 A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci. NHGRI|-1
NM_001013619 AGPHD1 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs28675338 1.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001013620 ALG10B 19483685 http://www.ncbi.nlm.nih.gov/pubmed/19483685 Drug-Induced Liver Injury rs6582630 1.00E-06 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. NHGRI|-1
NM_001013625 C1orf192 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs10800309 3.00E-09 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_001013663 C2orf79 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs41523444 1.63E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001013672 C17orf97 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4247113 2.62E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001013672 C17orf97 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4130140 2.30E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001013717 C5orf56 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs2188962 1.00E-07 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_001013717 C5orf56 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2188962 2.00E-18 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001013717 C5orf56 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs12521868 1.00E-20 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001013717 C5orf56 20031576 http://www.ncbi.nlm.nih.gov/pubmed/20031576 Fibrinogen rs2522056 1.00E-15 Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. NHGRI|-1
NM_001013717 C5orf56 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs6596075 3.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001013717 C5orf56 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs1016988 1.00E-12 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_001013836 MAD1L1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs6952808 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001013836 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11764337 3.86E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001013836 MAD1L1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4721135 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001013836 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4721295 2.21E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001013836 MAD1L1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs1107592 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001013836 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1107592 3.85E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001013836 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10224497 4.88E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001013836 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs3800917 2.47E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001013837 MAD1L1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs6952808 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001013837 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11764337 3.86E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001013837 MAD1L1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4721135 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001013837 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4721295 2.21E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001013837 MAD1L1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs1107592 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001013837 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1107592 3.85E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001013837 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10224497 4.88E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001013837 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs3800917 2.47E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001013843 SLTM 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs7179456 7.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_001013848 EXOC6 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs1111875 3.00E-06 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001013848 EXOC6 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1111875 6.00E-10 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001013848 EXOC6 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs1111875 6.00E-10 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001013848 EXOC6 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs1111875 7.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001013848 EXOC6 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs5015480 1.00E-15 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001013848 EXOC6 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs5015480 5.00E-06 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001013848 EXOC6 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs5015480 7.00E-08 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001013848 EXOC6 20862305 http://www.ncbi.nlm.nih.gov/pubmed/20862305 "Diabetes Mellitus, Type 2" rs5015480 9.00E-06 Identification of new genetic risk variants for type 2 diabetes. NHGRI|-1
NM_001013848 EXOC6 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs2497306 5.00E-09 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001014342 FLG2 21666691 http://www.ncbi.nlm.nih.gov/pubmed/21666691 "Dermatitis, Atopic" rs3126085 6.00E-12 Genome-wide association study identifies two new susceptibility loci for atopic dermatitis in the Chinese Han population. NHGRI|-1
NM_001014342 FLG2 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Exploratory Behavior rs3120665 4.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_001014380 KATNAL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17505148 7.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001014380 KATNAL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17724817 3.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001014380 KATNAL1 20460270 http://www.ncbi.nlm.nih.gov/pubmed/20460270 Biliary Atresia rs9314986 2.00E-06 Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. NHGRI|-1
NM_001014437 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs729662 8.52E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001014437 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7481584 9.54E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001014437 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001014437 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 4.55E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001014437 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 7.54E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001014437 CARS 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs739401 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001014437 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs438384 1.07E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001014437 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 2.60E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001014437 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 3.06E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001014437 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 9.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001014437 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs369461 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001014437 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs369461 7.87E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001014440 ODF3B 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs131794 1.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001014447 CPZ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4696715 5.58E-07 NBL-GWAS version 2 dbGaP|2895
NM_001014448 CPZ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4696715 5.58E-07 NBL-GWAS version 2 dbGaP|2895
NM_001014797 KCNMA1 21708048 http://www.ncbi.nlm.nih.gov/pubmed/21708048 Obesity rs2116830 3.00E-10 Genome Wide Association Study Identifies KCNMA1 Contributing to Human Obesity. NHGRI|-1
NM_001014797 KCNMA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1247755 7.47E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001014797 KCNMA1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2917454 3.30E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001014797 KCNMA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12219105 9.68E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001014797 KCNMA1 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs4979906 7.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_001014809 CRMP1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4292278 7.31E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs505102 1.07E-40 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs505102 9.09E-46 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs800292 1.68E-07 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs800292 2.21E-47 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs800292 5.05E-11 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs800292 9.78E-42 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001014975 CFH 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs1329424 6.00E-16 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs572515 1.22E-15 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs572515 4.10E-21 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3766404 2.44E-21 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3766404 2.50E-23 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7529589 1.60E-14 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7529589 2.67E-19 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001014975 CFH 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs1061170 1.00E-261 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001014975 CFH 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs1061170 4.00E-117 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801555 1.33E-71 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801555 3.74E-84 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10754199 1.17E-85 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10754199 7.71E-73 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12038333 2.77E-20 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12038333 4.47E-15 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2019727 2.99E-12 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2019724 2.07E-88 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2019724 9.52E-75 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001014975 CFH 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs10737680 2.00E-76 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs203674 1.29E-25 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs203674 6.04E-18 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001014975 CFH 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 "Glomerulonephritis, IGA" rs6677604 3.00E-10 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6677604 1.65E-32 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6677604 9.46E-38 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs419137 1.06E-10 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs419137 2.33E-09 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001014975 CFH 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs1410996 2.00E-111 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs380390 1.75E-19 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs380390 4.00E-08 Complement factor H polymorphism in age-related macular degeneration. NHGRI|-1
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2284664 2.28E-36 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2284664 2.81E-41 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1329428 1.35E-16 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001014975 CFH 20861866 http://www.ncbi.nlm.nih.gov/pubmed/20861866 Macular Degeneration rs1329428 3.00E-64 Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. NHGRI|-1
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1329428 6.93E-76 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001014975 CFH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1329428 8.92E-92 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001014986 FOLH1B 20801717 http://www.ncbi.nlm.nih.gov/pubmed/20801717 Amyotrophic Lateral Sclerosis rs1488902 3.00E-06 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. NHGRI|-1
NM_001015 RPS11 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Proteins rs2280401 3.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001015045 FAM13A 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs2869967 1.00E-07 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001015045 FAM13A 20173748 http://www.ncbi.nlm.nih.gov/pubmed/20173748 "Pulmonary Disease, Chronic Obstructive" rs7671167 1.00E-11 Variants in FAM13A are associated with chronic obstructive pulmonary disease. NHGRI|-1
NM_001015045 FAM13A 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Cornea rs16996151 6.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_001015051 RUNX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4714860 7.86E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001015053 HDAC5 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs228769 2.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001015053 HDAC5 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs228769 4.00E-06 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001015072 UFSP1 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs12666989 2.00E-08 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_001015880 PAPSS2 19727025 http://www.ncbi.nlm.nih.gov/pubmed/19727025 Exercise rs10887741 4.00E-06 Genome-wide association study of exercise behavior in Dutch and American adults. NHGRI|-1
NM_001015887 IGSF11 17903300 http://www.ncbi.nlm.nih.gov/pubmed/17903300 Waist Circumference rs1875517 2.00E-06 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. NHGRI|-1
NM_001015887 IGSF11 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs6438424 1.00E-13 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001017364 C4BPB 20212171 http://www.ncbi.nlm.nih.gov/pubmed/20212171 Complement C4b-Binding Protein rs3813948 4.00E-10 C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies. NHGRI|-1
NM_001017365 C4BPB 20212171 http://www.ncbi.nlm.nih.gov/pubmed/20212171 Complement C4b-Binding Protein rs3813948 4.00E-10 C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies. NHGRI|-1
NM_001017366 C4BPB 20212171 http://www.ncbi.nlm.nih.gov/pubmed/20212171 Complement C4b-Binding Protein rs3813948 4.00E-10 C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies. NHGRI|-1
NM_001017367 C4BPB 20212171 http://www.ncbi.nlm.nih.gov/pubmed/20212171 Complement C4b-Binding Protein rs3813948 4.00E-10 C4BPB/C4BPA is a new susceptibility locus for venous thrombosis with unknown protein S-independent mechanism: results from genome-wide association and gene expression analyses followed by case-control studies. NHGRI|-1
NM_001017372 SLC27A6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12523161 9.20E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001017388 TLR10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6838905 6.46E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001017388 TLR10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6838905 7.66E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001017388 TLR10 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7658334 1.49E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001017424 KCNK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1377185 3.16E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001017424 KCNK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs556648 3.84E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001017425 KCNK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1377185 3.16E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001017425 KCNK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs556648 3.84E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001017523 BTBD11 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4964213 1.75E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001017915 INPP5D 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs10933436 7.00E-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001017923 C14orf28 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs17115674 7.76E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001017930 DCAF8L1 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs5971305 8.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001017961 FAM78B 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs10753713 3.47E-06 NBL-GWAS version 1 dbGaP|2845
NM_001017964 YDJC 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs2298428 3.00E-10 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_001017964 YDJC 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs2298428 2.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001017971 ATP6AP1L 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs1032757 2.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_001017971 ATP6AP1L 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1423515 1.61E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001017973 P4HA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4594848 7.35E-05 NBL-GWAS version 2 dbGaP|2895
NM_001017974 P4HA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4594848 7.35E-05 NBL-GWAS version 2 dbGaP|2895
NM_001017975 HFM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs469846 3.43E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001017975 HFM1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs164898 6.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001017980 VMA21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6627154 7.13E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001017980 VMA21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs5969786 7.52E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001017992 ACTBL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1454909 4.31E-05 NBL-GWAS version 2 dbGaP|2895
NM_001017992 ACTBL2 21190210 http://www.ncbi.nlm.nih.gov/pubmed/21190210 Obsessive-Compulsive Disorder rs1844437 2.00E-06 Genome-wide association study of hoarding traits. NHGRI|-1
NM_001018003 SORBS3 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs4872511 9.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_001018003 SORBS3 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs2280890 9.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_001018004 TPM1 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs11071720 2.00E-08 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001018005 TPM1 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs11071720 2.00E-08 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001018006 TPM1 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs11071720 2.00E-08 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001018007 TPM1 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs11071720 2.00E-08 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001018008 TPM1 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs11071720 2.00E-08 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001018011 ZBTB16 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs17116334 9.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001018016 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001018016 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001018017 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001018017 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001018020 TPM1 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs11071720 2.00E-08 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001018036 TSHR 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs17111394 4.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_001018036 TSHR 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs8017455 6.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001018037 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11145323 7.08E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001018037 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2150901 5.11E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001018037 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2183863 4.74E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001018037 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7030802 7.12E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001018037 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1574144 3.30E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001018038 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11145323 7.08E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001018038 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2150901 5.11E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001018038 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2183863 4.74E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001018038 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7030802 7.12E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001018038 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1574144 3.30E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001018039 SFMBT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs4748940 3.09E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001018039 SFMBT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1417032 1.94E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001018039 SFMBT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2486866 1.53E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001018039 SFMBT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2462692 1.57E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001018046 YSK4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6754977 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001018053 PFKFB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2243816 9.18E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001018054 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs5177 5.00E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001018054 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11206127 3.16E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001018054 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs869987 4.54E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001018054 LRP8 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs114216682 7.00E-08 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001018054 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17785382 1.74E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001018058 TFEC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1464776 1.55E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001018058 TFEC 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12673240 8.31E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001018064 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1034042 1.58E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018064 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769612 1.60E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018064 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769605 9.38E-06 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018064 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769600 1.35E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018064 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769595 1.17E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018064 NTRK2 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs2841498 4.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_001018065 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1034042 1.58E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018065 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769612 1.60E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018065 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769605 9.38E-06 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018065 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769600 1.35E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018065 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769595 1.17E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018065 NTRK2 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs2841498 4.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_001018066 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1034042 1.58E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018066 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769612 1.60E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018066 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769605 9.38E-06 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018066 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769600 1.35E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018066 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769595 1.17E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001018066 NTRK2 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs2841498 4.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_001018072 BTBD11 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4964213 1.75E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001018088 VPS13C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4143844 4.93E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001018088 VPS13C 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs17271305 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001018088 VPS13C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs3934516 5.53E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001018090 GCOM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs937254 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001018090 GCOM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs935549 3.91E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001018090 GCOM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs744318 3.60E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001018091 GCOM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs937254 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001018091 GCOM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs935549 3.91E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001018091 GCOM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs744318 3.60E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001018100 GCOM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs937254 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001018100 GCOM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs935549 3.91E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001018100 GCOM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs744318 3.60E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001018102 GRINL1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs597804 5.59E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001018102 GRINL1A 19609347 http://www.ncbi.nlm.nih.gov/pubmed/19609347 Hypertension rs1550576 3.00E-06 A genome-wide association study of hypertension and blood pressure in African Americans. NHGRI|-1
NM_001018112 FANCA 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12931267 3.00E-10 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001018112 FANCA 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12931267 5.00E-87 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001018112 FANCA 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Melanosis rs12931267 8.00E-62 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001018112 FANCA 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs16966142 6.00E-06 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_001018116 MURC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs13285273 5.75E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001020658 PUM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7536851 2.29E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001020658 PUM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10753241 2.20E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001020658 PUM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10753242 2.16E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001020658 PUM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7526662 1.86E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001023563 ZNF805 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs2014572 7.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001023567 GOLGA8B 20835239 http://www.ncbi.nlm.nih.gov/pubmed/20835239 Refractive Errors rs634990 2.00E-14 A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14. NHGRI|-1
NM_001024465 SOD2 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs4516970 1.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001024466 SOD2 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs4516970 1.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001024594 C1orf53 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs12134279 2.00E-14 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001024594 C1orf53 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922306 1.79E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001024594 C1orf53 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922306 7.55E-07 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001024594 C1orf53 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922313 3.56E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001024594 C1orf53 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922313 4.57E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001024628 NRP1 21682944 http://www.ncbi.nlm.nih.gov/pubmed/21682944 Schizophrenia rs1412115 6.00E-06 DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population. NHGRI|-1
NM_001024629 NRP1 21682944 http://www.ncbi.nlm.nih.gov/pubmed/21682944 Schizophrenia rs1412115 6.00E-06 DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population. NHGRI|-1
NM_001024630 RUNX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4714860 7.86E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001024644 XCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10510749 4.22E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001024644 XCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7631551 7.95E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001024644 XCR1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs13098911 3.00E-17 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001024666 SH3KBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs16997315 4.66E-11 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001024674 LIN52 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Circadian Rhythm rs2239557 3.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001024736 CD276 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs1038094 9.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_001024843 TNRC6B 19117981 http://www.ncbi.nlm.nih.gov/pubmed/19117981 Prostatic Neoplasms rs9623117 5.00E-07 Sequence variants at 22q13 are associated with prostate cancer risk. NHGRI|-1
NM_001024843 TNRC6B 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs12484776 3.00E-12 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_001024843 TNRC6B 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Body Height rs139909 2.00E-07 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_001024843 TNRC6B 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs6001877 7.17E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001024847 TGFBR2 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs3773643 2.00E-07 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001024847 TGFBR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2043136 9.09E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001024847 TGFBR2 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs4680878 7.50E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001024847 TGFBR2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9870410 3.76E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001024847 TGFBR2 17903298 http://www.ncbi.nlm.nih.gov/pubmed/17903298 Blood Glucose rs10510634 5.00E-06 Genome-wide association with diabetes-related traits in the Framingham Heart Study. NHGRI|-1
NM_001024847 TGFBR2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1117751 1.98E-06 NBL-GWAS version 1 dbGaP|2845
NM_001024847 TGFBR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4613502 1.65E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001024858 SPTB 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs229673 6.70E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001024858 SPTB 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2285002 1.43E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001024924 EXOC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4333263 1.12E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001024924 EXOC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs13120644 6.72E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001024948 FNBP1L 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs237438 5.24E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001024948 FNBP1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs237425 9.56E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001025076 CELF2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs3780993 6.86E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001025076 CELF2 21379329 http://www.ncbi.nlm.nih.gov/pubmed/21379329 Alzheimer Disease rs62209 2.00E-07 Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE. NHGRI|-1
NM_001025077 CELF2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs3780993 6.86E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001025077 CELF2 21379329 http://www.ncbi.nlm.nih.gov/pubmed/21379329 Alzheimer Disease rs62209 2.00E-07 Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE. NHGRI|-1
NM_001025087 CELF4 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs4799915 3.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001025087 CELF4 19359265 http://www.ncbi.nlm.nih.gov/pubmed/19359265 Telomere rs2162440 3.00E-06 A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere length. NHGRI|-1
NM_001025088 CELF4 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs4799915 3.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001025088 CELF4 19359265 http://www.ncbi.nlm.nih.gov/pubmed/19359265 Telomere rs2162440 3.00E-06 A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere length. NHGRI|-1
NM_001025089 CELF4 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs4799915 3.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001025089 CELF4 19359265 http://www.ncbi.nlm.nih.gov/pubmed/19359265 Telomere rs2162440 3.00E-06 A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere length. NHGRI|-1
NM_001025091 ABCF1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3132610 1.15E-08 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001025105 CSNK1A1 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs10058728 5.00E-09 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001025105 CSNK1A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17796714 1.02E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001025108 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs13385193 2.82E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001025108 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17437101 6.31E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001025108 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6736239 5.21E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001025108 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17352801 8.79E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001025108 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6743817 2.70E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001025108 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10199628 2.67E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001025108 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17023516 3.31E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001025108 AFF3 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs11676922 1.00E-14 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001025108 AFF3 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs9653442 5.00E-06 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_001025108 AFF3 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs10865035 2.00E-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001025109 CD34 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs2745967 7.00E-08 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_001025160 CD97 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs4528684 1.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_001025197 CHI3L2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17654531 1.16E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001025199 CHI3L2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17654531 1.16E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001025200 CTRB2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs7202877 3.00E-15 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001025200 CTRB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7202877 3.59E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001025232 CLLU1OS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs402436 1.98E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001025233 CLLU1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10219495 5.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001025248 DUT 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Adiponectin rs11637235 3.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001025249 DUT 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Adiponectin rs11637235 3.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001025266 C3orf70 21042317 http://www.ncbi.nlm.nih.gov/pubmed/21042317 "Depressive Disorder, Major" rs7647854 5.00E-06 "Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned." NHGRI|-1
NM_001025290 DPPA5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs9360664 8.27E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001025356 ANO6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12579771 2.29E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001025357 C8orf85 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs720133 3.20E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001025366 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001025366 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001025366 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001025366 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001025366 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001025367 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001025367 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001025367 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001025367 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001025367 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001025368 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001025368 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001025368 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001025368 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001025368 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001025369 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001025369 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001025369 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001025369 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001025369 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001025370 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001025370 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001025370 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001025370 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001025370 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001025389 AMPD3 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Bipolar Disorder rs6484218 4.00E-08 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_001025390 AMPD3 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Bipolar Disorder rs6484218 4.00E-08 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_001025616 ARHGAP24 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs7692808 6.00E-20 Genome-wide association study of PR interval. NHGRI|-1
NM_001025616 ARHGAP24 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs7660702 3.00E-17 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001025616 ARHGAP24 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs345328 2.91E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001026 RPS24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1916400 1.80E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001026 RPS24 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs2395528 6.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001026 RPS24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs35648 3.27E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001029 RPS26 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs12580100 1.00E-06 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_001029 RPS26 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs11171739 1.00E-11 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001029851 PDE8B 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs4457053 3.00E-12 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001029852 PDE8B 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs4457053 3.00E-12 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001029853 PDE8B 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs4457053 3.00E-12 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001029854 PDE8B 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs4457053 3.00E-12 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001029858 SLC35F1 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs281868 4.00E-10 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_001029858 SLC35F1 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs89107 1.00E-09 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_001029880 SFMBT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs4748940 3.09E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001029880 SFMBT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1417032 1.94E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001029880 SFMBT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2486866 1.53E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001029880 SFMBT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2462692 1.57E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001029883 C2orf71 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs882632 2.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_001029884 PLEKHG1 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs9372078 5.00E-07 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_001029887 HELT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6818704 4.66E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001029939 ZFAT 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1036819 1.00E-24 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001029939 ZFAT 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs12680655 2.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001029939 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1545240 1.52E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001029939 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs16905215 1.89E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001029939 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs9785140 1.26E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001029996 PCDP1 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2587695 3.00E-07 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_001030003 HNF4A 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs1800961 8.00E-10 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001030003 HNF4A 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs1800961 2.00E-09 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001030003 HNF4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs1800961 7.13E-07 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_001030003 HNF4A 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6017342 1.00E-20 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001030003 HNF4A 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs6017342 9.00E-17 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_001030004 HNF4A 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs1800961 8.00E-10 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001030004 HNF4A 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs1800961 2.00E-09 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001030004 HNF4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs1800961 7.13E-07 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_001030004 HNF4A 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6017342 1.00E-20 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001030004 HNF4A 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs6017342 9.00E-17 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_001030005 CPLX3 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs6495122 2.00E-10 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001030005 CPLX3 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs6495122 6.00E-07 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_001030013 NPS 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11018214 2.99E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001030013 NPS 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4363506 4.79E-07 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001030013 NPS 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4363506 7.00E-07 Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_001030013 NPS 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10830099 1.73E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001030013 NPS 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10765118 1.25E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001030019 SUN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2708909 3.44E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001030047 KLK3 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs17632542 3.00E-46 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001030047 KLK3 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs2735839 2.00E-18 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_001030047 KLK3 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs266849 6.00E-10 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001030048 KLK3 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs17632542 3.00E-46 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001030048 KLK3 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs2735839 2.00E-18 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_001030048 KLK3 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs266849 6.00E-10 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001030050 KLK3 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs17632542 3.00E-46 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001030050 KLK3 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs2735839 2.00E-18 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_001030050 KLK3 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs266849 6.00E-10 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001030060 SAMD5 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs9390537 8.00E-06 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_001030060 SAMD5 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs9497975 7.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001030060 SAMD5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs325105 1.95E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001030272 ARNTL 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs900145 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001030273 ARNTL 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs900145 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001030311 CERKL 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs993648 3.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001030312 CERKL 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs993648 3.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001030313 CERKL 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs993648 3.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001031672 CYB5RL 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7520966 6.54E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001031672 CYB5RL 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs682705 2.20E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001031679 MSRB3 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs10506525 6.00E-09 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001031679 MSRB3 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs10506525 9.00E-07 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001031679 MSRB3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10784460 2.18E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001031679 MSRB3 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic Nephropathies rs2358944 4.00E-06 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_001031680 RUNX3 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs11249215 9.00E-11 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_001031680 RUNX3 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs10903122 2.00E-10 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001031689 PLAA 20185149 http://www.ncbi.nlm.nih.gov/pubmed/20185149 Schizophrenia rs7045881 2.00E-06 Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. NHGRI|-1
NM_001031694 SCMH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs6686842 2.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001031701 NT5DC3 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs4964805 5.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_001031702 SEMA5B 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs9868873 1.00E-07 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001031709 RNLS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2162361 4.54E-06 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001031709 RNLS 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs10509540 1.00E-28 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001031715 IQCH 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7359257 2.00E-06 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001031720 GSTCD 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs10516526 2.00E-23 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_001031725 DDX59 19389651 http://www.ncbi.nlm.nih.gov/pubmed/19389651 Electrocardiography rs7512898 5.00E-06 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. NHGRI|-1
NM_001031726 C19orf12 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs8102137 2.00E-11 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_001031746 C10orf72 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs2244967 5.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_001031801 LIMK2 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic Nephropathies rs2106294 4.00E-06 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_001031804 MAF 19151714 http://www.ncbi.nlm.nih.gov/pubmed/19151714 Obesity rs1424233 4.00E-13 Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. NHGRI|-1
NM_001031804 MAF 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs17767419 9.00E-15 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001031804 MAF 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs3813579 4.00E-10 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001031804 MAF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1396702 6.06E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001031804 MAF 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4888984 4.71E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001031804 MAF 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4888984 9.48E-06 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001031804 MAF 20668459 http://www.ncbi.nlm.nih.gov/pubmed/20668459 Body Height rs7498403 5.00E-06 Genetic variants that affect length/height in infancy/early childhood in Vietnamese-Korean families. NHGRI|-1
NM_001031853 INSC 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7117858 6.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001031853 INSC 21104366 http://www.ncbi.nlm.nih.gov/pubmed/21104366 Bone Density rs11023787 5.00E-16 A genome-wide association analysis implicates SOX6 as a candidate gene for wrist bone mass. NHGRI|-1
NM_001032281 TFPI 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs7586970 9.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_001032281 TFPI 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1520475 8.56E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001032283 TMPO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs249851 1.20E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001032284 TMPO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs249851 1.20E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001032291 PSRC1 20442857 http://www.ncbi.nlm.nih.gov/pubmed/20442857 1-Alkyl-2-acetylglycerophosphocholine Esterase rs599839 3.00E-15 Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study. NHGRI|-1
NM_001032291 PSRC1 18262040 http://www.ncbi.nlm.nih.gov/pubmed/18262040 "Cholesterol, LDL" rs599839 1.00E-33 LDL-cholesterol concentrations: a genome-wide association study. NHGRI|-1
NM_001032291 PSRC1 18179892 http://www.ncbi.nlm.nih.gov/pubmed/18179892 "Cholesterol, LDL" rs599839 1.00E-07 Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. NHGRI|-1
NM_001032291 PSRC1 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs599839 6.00E-33 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001032291 PSRC1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs599839 3.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001032291 PSRC1 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs599839 4.00E-09 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_001032296 STK24 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs9517320 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001032363 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 2.00E-11 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001032363 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 3.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001032363 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12138950 3.00E-18 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001032363 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs10917468 1.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001032364 GGT1 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs4820599 4.00E-11 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_001032364 GGT1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 gamma-Glutamyltransferase rs5751901 2.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001032365 GGT1 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs4820599 4.00E-11 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_001032365 GGT1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 gamma-Glutamyltransferase rs5751901 2.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001032386 SUOX 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs1701704 3.00E-08 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_001032386 SUOX 18198356 http://www.ncbi.nlm.nih.gov/pubmed/18198356 "Diabetes Mellitus, Type 1" rs1701704 9.00E-10 A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study. NHGRI|-1
NM_001032387 SUOX 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs1701704 3.00E-08 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_001032387 SUOX 18198356 http://www.ncbi.nlm.nih.gov/pubmed/18198356 "Diabetes Mellitus, Type 1" rs1701704 9.00E-10 A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study. NHGRI|-1
NM_001032394 GPR126 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs6570507 2.00E-07 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_001032394 GPR126 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs6570507 4.00E-11 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001032394 GPR126 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs4896582 2.00E-18 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001032394 GPR126 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs3817928 1.00E-09 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001032394 GPR126 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs3748069 5.00E-14 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001032394 GPR126 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs9496398 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001032394 GPR126 21060863 http://www.ncbi.nlm.nih.gov/pubmed/21060863 Retinal Vein rs225717 1.00E-16 "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo." NHGRI|-1
NM_001032395 GPR126 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs6570507 2.00E-07 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_001032395 GPR126 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs6570507 4.00E-11 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001032395 GPR126 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs4896582 2.00E-18 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001032395 GPR126 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs3817928 1.00E-09 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001032395 GPR126 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs3748069 5.00E-14 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001032395 GPR126 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs9496398 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001032395 GPR126 21060863 http://www.ncbi.nlm.nih.gov/pubmed/21060863 Retinal Vein rs225717 1.00E-16 "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo." NHGRI|-1
NM_001032998 KYNU 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs352892 5.04E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001032998 KYNU 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2890652 1.00E-10 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001033024 FBXO7 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9609565 4.00E-10 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001033028 CYFIP1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs6606803 4.89E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001033046 C17orf62 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Insulin-Like Growth Factor I rs9303029 4.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001033057 MAGI1 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6795735 2.00E-16 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001033057 MAGI1 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs4607103 1.00E-08 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001033057 MAGI1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10510933 3.46E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001033083 PBLD 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1900004 2.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_001033083 PBLD 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1900004 3.00E-35 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_001033083 PBLD 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs3858145 2.00E-07 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_001033083 PBLD 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Optic Disk rs3858145 3.00E-10 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_001033083 PBLD 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Optic Disk rs12571093 2.00E-10 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_001033087 MACROD2 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs6079395 7.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001033087 MACROD2 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs6110278 4.00E-07 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001033087 MACROD2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6079482 4.19E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001033087 MACROD2 20663923 http://www.ncbi.nlm.nih.gov/pubmed/20663923 Autistic Disorder rs4141463 4.00E-08 A genome-wide scan for common alleles affecting risk for autism. NHGRI|-1
NM_001033087 MACROD2 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs6110577 5.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_001033087 MACROD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6043422 8.97E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001033087 MACROD2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6043600 6.18E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001033117 SRGAP3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2600178 1.52E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001033504 TMEM98 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9904938 7.03E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001033549 C19orf62 20852631 http://www.ncbi.nlm.nih.gov/pubmed/20852631 Breast Neoplasms rs8170 2.00E-09 A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population. NHGRI|-1
NM_001033549 C19orf62 20852633 http://www.ncbi.nlm.nih.gov/pubmed/20852633 Ovarian Neoplasms rs8170 4.00E-06 Common variants at 19p13 are associated with susceptibility to ovarian cancer. NHGRI|-1
NM_001033581 PRKCZ 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs3753242 1.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001033582 PRKCZ 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs3753242 1.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001033602 MTUS2 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Attention Deficit Disorder with Hyperactivity rs1161463 2.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001033756 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001033756 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001033756 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001033756 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001033756 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001033886 CXCL12 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs501120 9.00E-08 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_001033886 CXCL12 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs1746048 3.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001033886 CXCL12 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs1746048 7.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_001033910 TRAF5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3738200 4.83E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001033910 TRAF5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17189000 5.44E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001034172 MCART2 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs10438933 1.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001034837 KCNIP1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs11957313 9.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001034838 KCNIP1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs11957313 9.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001034842 PTCHD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10829219 2.55E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001034845 GALNTL6 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs7660673 8.92E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001034850 FAM134B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs26015 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001034850 FAM134B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs16868670 2.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001034852 SMOC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs227446 9.90E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001035 RYR2 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs7554607 2.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001035 RYR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs10925500 2.58E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001035 RYR2 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 Exercise Test rs2819770 4.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_001035 RYR2 21386754 http://www.ncbi.nlm.nih.gov/pubmed/21386754 Rhabdomyolysis rs2819742 2.00E-07 "Cerivastatin, genetic variants, and the risk of rhabdomyolysis." NHGRI|-1
NM_001035003 KCNIP4 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4697177 6.80E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001035003 KCNIP4 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs6825103 2.13E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001035003 KCNIP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs876477 5.40E-06 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001035003 KCNIP4 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs358592 3.00E-06 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_001035003 KCNIP4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4697227 1.84E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001035004 KCNIP4 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4697177 6.80E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001035004 KCNIP4 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs6825103 2.13E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001035004 KCNIP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs876477 5.40E-06 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001035004 KCNIP4 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs358592 3.00E-06 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_001035004 KCNIP4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4697227 1.84E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001035005 C18orf32 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs8099594 3.00E-07 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001035258 RPL38 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7219464 1.67E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001036 RYR3 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Carotid Artery Diseases rs2229116 3.00E-08 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_001036 RYR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6495001 8.90E-05 NBL-GWAS version 2 dbGaP|2895
NM_001037126 EXOC4 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs10488172 8.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001037132 NRCAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs409797 8.78E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001037164 ARL4A 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs732577 4.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001037165 FOXK1 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Factor VII rs10488360 7.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001037290 BCO2 20150558 http://www.ncbi.nlm.nih.gov/pubmed/20150558 Interleukin-18 rs2115763 4.00E-09 Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels. NHGRI|-1
NM_001037290 BCO2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Interleukin-18 rs2250417 7.00E-13 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001037317 LPPR5 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1351563 7.27E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001037324 ECE2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs3914188 3.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001037325 CCDC46 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs8074751 1.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_001037325 CCDC46 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs7209395 3.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001037325 CCDC46 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs757558 6.42E-06 NBL-GWAS version 1 dbGaP|2845
NM_001037331 C18orf62 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7235563 9.13E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001037331 C18orf62 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs3213875 9.37E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001037331 C18orf62 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7233038 3.43E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001037331 C18orf62 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11150911 7.69E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001037331 C18orf62 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1460277 1.50E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001037331 C18orf62 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2048135 2.86E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001037339 PDE4B 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 "Atrial Function, Left" rs10493389 7.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_001037339 PDE4B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs11208807 3.63E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001037339 PDE4B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2069278 2.18E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001037339 PDE4B 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs1892534 7.00E-21 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_001037339 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs1892534 4.77E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001037339 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs2889195 5.95E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001037339 PDE4B 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4420065 4.00E-62 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001037339 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs4420065 6.67E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001037339 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs12753193 3.76E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001037339 PDE4B 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Inflammation rs12753193 4.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001037340 PDE4B 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 "Atrial Function, Left" rs10493389 7.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_001037340 PDE4B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs11208807 3.63E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001037340 PDE4B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2069278 2.18E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001037340 PDE4B 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs1892534 7.00E-21 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_001037340 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs1892534 4.77E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001037340 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs2889195 5.95E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001037340 PDE4B 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4420065 4.00E-62 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001037340 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs4420065 6.67E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001037340 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs12753193 3.76E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001037340 PDE4B 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Inflammation rs12753193 4.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001037341 PDE4B 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 "Atrial Function, Left" rs10493389 7.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_001037341 PDE4B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs11208807 3.63E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001037341 PDE4B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2069278 2.18E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001037341 PDE4B 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs1892534 7.00E-21 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_001037341 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs1892534 4.77E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001037341 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs2889195 5.95E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001037341 PDE4B 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4420065 4.00E-62 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001037341 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs4420065 6.67E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001037341 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs12753193 3.76E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001037341 PDE4B 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Inflammation rs12753193 4.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001037442 RUFY3 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7686646 9.64E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001037442 RUFY3 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs6815629 9.64E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001037498 DEFB112 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2894779 2.25E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001037525 GALC 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs11624056 3.00E-08 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001037525 GALC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1385397 5.84E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001037525 GALC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2401711 9.82E-05 NBL-GWAS version 2 dbGaP|2895
NM_001037525 GALC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7152233 7.28E-06 NBL-GWAS version 2 dbGaP|2895
NM_001037631 CTLA4 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs3087243 1.00E-08 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001037631 CTLA4 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs3087243 1.00E-15 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001037631 CTLA4 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs3087243 8.00E-11 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_001037631 CTLA4 19503088 http://www.ncbi.nlm.nih.gov/pubmed/19503088 "Arthritis, Rheumatoid" rs231735 6.00E-09 "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis." NHGRI|-1
NM_001037631 CTLA4 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs1024161 4.00E-13 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_001037671 C12orf74 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10219495 5.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001037763 COL28A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2159710 5.50E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001037763 COL28A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10486158 3.39E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001037763 COL28A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7800159 2.42E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001037763 COL28A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4724977 1.78E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001037763 COL28A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10486156 3.69E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001037763 COL28A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2881814 4.90E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001037763 COL28A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6955140 4.99E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001037984 SLC38A10 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs10445407 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001038 SCNN1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10849446 3.66E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001038 SCNN1A 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs11064153 5.39E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001039112 FER1L6 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10808533 3.05E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001039112 FER1L6 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs10481151 4.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001039132 ICAM4 18604267 http://www.ncbi.nlm.nih.gov/pubmed/18604267 Intercellular Adhesion Molecule-1 rs5498 5.00E-25 "Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women." NHGRI|-1
NM_001039132 ICAM4 21533024 http://www.ncbi.nlm.nih.gov/pubmed/21533024 Intercellular Adhesion Molecule-1 rs5498 6.00E-89 "Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci." NHGRI|-1
NM_001039132 ICAM4 18604267 http://www.ncbi.nlm.nih.gov/pubmed/18604267 Intercellular Adhesion Molecule-1 rs281437 3.00E-10 "Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women." NHGRI|-1
NM_001039132 ICAM4 20167578 http://www.ncbi.nlm.nih.gov/pubmed/20167578 Intercellular Adhesion Molecule-1 rs3093030 4.00E-23 Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. NHGRI|-1
NM_001039141 TRIOBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs16985637 3.13E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001039152 RGS21 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs2816316 2.00E-17 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001039152 RGS21 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs2816316 3.00E-11 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_001039348 EFEMP1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs3791679 6.00E-11 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001039348 EFEMP1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs3791679 6.00E-09 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001039348 EFEMP1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs3791675 2.00E-12 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001039348 EFEMP1 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Body Height rs3791675 2.00E-09 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001039348 EFEMP1 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs3791675 3.00E-07 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_001039348 EFEMP1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs3791675 4.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001039348 EFEMP1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs6751715 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001039348 EFEMP1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs7577894 1.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001039349 EFEMP1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs3791679 6.00E-11 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001039349 EFEMP1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs3791679 6.00E-09 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001039349 EFEMP1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs3791675 2.00E-12 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001039349 EFEMP1 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Body Height rs3791675 2.00E-09 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001039349 EFEMP1 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs3791675 3.00E-07 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_001039349 EFEMP1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs3791675 4.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001039349 EFEMP1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs6751715 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001039349 EFEMP1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs7577894 1.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001039350 DPP6 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs6464375 4.00E-07 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_001039350 DPP6 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10260404 3.00E-06 A genome-wide association study of sporadic ALS in a homogenous Irish population. NHGRI|-1
NM_001039350 DPP6 18987618 http://www.ncbi.nlm.nih.gov/pubmed/18987618 Amyotrophic Lateral Sclerosis rs10260404 3.00E-06 Screening for replication of genome-wide SNP associations in sporadic ALS. NHGRI|-1
NM_001039350 DPP6 18084291 http://www.ncbi.nlm.nih.gov/pubmed/18084291 Amyotrophic Lateral Sclerosis rs10260404 5.00E-08 Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis. NHGRI|-1
NM_001039350 DPP6 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6952728 5.15E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001039366 ATP6V1E1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9604779 5.29E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001039367 ATP6V1E1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9604779 5.29E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001039459 ELMO1 17653210 http://www.ncbi.nlm.nih.gov/pubmed/17653210 Diabetic Nephropathies rs741301 8.00E-06 Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population. NHGRI|-1
NM_001039459 ELMO1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs10488031 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001039459 ELMO1 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs4723619 3.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001039459 ELMO1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs6974491 2.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001039459 ELMO1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs6974491 4.00E-08 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001039459 ELMO1 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs11984075 5.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_001039508 SIRPG 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2281808 1.00E-11 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001039535 SKA1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2119547 3.65E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001039535 SKA1 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs1036935 2.00E-06 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_001039538 MAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9288410 2.71E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001039538 MAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9288410 3.28E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001039538 MAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9288410 5.64E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001039547 GK5 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs347685 3.00E-11 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001039573 SEC14L1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs3744064 7.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001039614 C15orf59 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs1038094 9.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_001039617 ZDHHC19 21160409 http://www.ncbi.nlm.nih.gov/pubmed/21160409 HIV-1 rs11924930 7.00E-06 Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population. NHGRI|-1
NM_001039651 C6orf26 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6905572 1.50E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001039753 EML6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs13401661 8.69E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001039753 EML6 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs6726292 1.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_001039753 EML6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2971884 7.79E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001039753 EML6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2941577 9.89E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001039753 EML6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2666035 4.88E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001039762 FAM196A 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4363506 4.79E-07 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001039762 FAM196A 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4363506 7.00E-07 Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_001039762 FAM196A 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10830099 1.73E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001039762 FAM196A 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10765118 1.25E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001039763 TMEM232 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs17132261 9.00E-07 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_001039763 TMEM232 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Plasminogen Activator Inhibitor 1 rs4460176 3.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001039802 CDC42 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2473323 3.13E-09 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001039803 CDK20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10868677 8.79E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001039885 FKRP 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs11668878 4.00E-07 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_001039936 CHN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs39059 5.91E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001040020 FAM3C 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Bone Density rs7776725 1.00E-11 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001040020 FAM3C 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Bone Density rs7776725 2.00E-06 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001040022 SIRPA 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs6136489 8.00E-11 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001040022 SIRPA 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs6045676 3.00E-08 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_001040023 SIRPA 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs6136489 8.00E-11 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001040023 SIRPA 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs6045676 3.00E-08 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_001040033 CD53 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7513168 1.49E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001040033 CD53 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1282020 8.95E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001040033 CD53 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1282023 8.95E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001040033 CD53 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1548342 8.72E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001040033 CD53 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6701134 6.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001040058 SPP1 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs2725236 5.00E-06 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_001040060 SPP1 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs2725236 5.00E-06 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_001040061 C3orf72 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs1511412 2.00E-13 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_001040092 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7000665 1.12E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001040092 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9643136 1.15E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001040092 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6993464 6.39E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001040092 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11782176 5.55E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001040092 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6991756 5.01E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001040097 MOSPD3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7786877 3.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001040098 MOSPD3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7786877 3.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001040099 MOSPD3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7786877 3.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001040109 MLN 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs2274459 6.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_001040118 ARAP1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs1552224 1.00E-22 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001040135 ACTR3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs56216502 4.67E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001040142 SCN2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2116658 1.48E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001040142 SCN2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs13025009 2.16E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001040142 SCN2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs764660 7.83E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001040143 SCN2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2116658 1.48E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001040143 SCN2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs13025009 2.16E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001040143 SCN2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs764660 7.83E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001040157 KIAA1712 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs6852435 6.00E-06 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_001040158 H2AFY 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs31198 8.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001040158 H2AFY 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs254560 1.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001040158 H2AFY 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs477687 6.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_001040159 SPOCK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7657608 2.65E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001040169 HTR4 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs11168048 1.00E-11 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001040169 HTR4 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs3995090 4.00E-09 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_001040172 HTR4 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs11168048 1.00E-11 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001040172 HTR4 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs3995090 4.00E-09 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_001040173 HTR4 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs11168048 1.00E-11 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001040173 HTR4 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs3995090 4.00E-09 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_001040177 AKR1E2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs6601764 9.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001040177 AKR1E2 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs2031577 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001040177 AKR1E2 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Mass Index rs10458787 1.00E-06 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_001040177 AKR1E2 20662065 http://www.ncbi.nlm.nih.gov/pubmed/20662065 Lupus Vulgaris rs1391511 7.00E-06 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. NHGRI|-1
NM_001040179 MCHR2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2841307 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001040179 MCHR2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs4840086 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001040179 MCHR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4431442 5.59E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001040194 AGTRAP 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs4846033 4.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_001040195 AGTRAP 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs4846033 4.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_001040196 AGTRAP 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs4846033 4.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_001040197 AGTRAP 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs4846033 4.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_001040202 PAQR3 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1455311 1.00E-18 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001040214 NKAIN2 20634892 http://www.ncbi.nlm.nih.gov/pubmed/20634892 Neurotic Disorders rs9491140 3.00E-07 A genome-wide association study of neuroticism in a population-based sample. NHGRI|-1
NM_001040214 NKAIN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs781484 1.83E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001040260 DCLK2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2654831 8.63E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001040261 DCLK2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2654831 8.63E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001040272 ADAMTSL1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10963676 1.76E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001040272 ADAMTSL1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10963676 4.79E-07 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001040272 ADAMTSL1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs10810865 4.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001040272 ADAMTSL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs1755289 9.84E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001040272 ADAMTSL1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1755289 3.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001040272 ADAMTSL1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1755289 9.10E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001040272 ADAMTSL1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs2210327 7.00E-07 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_001040274 SYCP2L 19448621 http://www.ncbi.nlm.nih.gov/pubmed/19448621 Menarche rs2153157 5.00E-08 Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. NHGRI|-1
NM_001040275 ESR2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1256065 8.27E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001040275 ESR2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1256059 4.61E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001040275 ESR2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1256044 4.68E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001040275 ESR2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1269056 5.46E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001040276 ESR2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1256065 8.27E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001040276 ESR2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1256059 4.61E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001040276 ESR2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1256044 4.68E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001040276 ESR2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1269056 5.46E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001040280 CD83 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2094923 2.89E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001040280 CD83 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2274822 1.56E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001040280 CD83 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs6914079 2.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_001040280 CD83 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs7770731 1.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001040280 CD83 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs6941421 6.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001040280 CD83 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12333130 5.60E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001040280 CD83 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1003024 6.43E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001040280 CD83 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs1003024 7.51E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_001040280 CD83 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1555051 7.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001040280 CD83 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs7750009 7.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001040282 TBC1D3G 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Chemokine CCL4 rs4796217 4.00E-21 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001040424 PRDM15 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs7279297 3.00E-06 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_001040428 SPATA7 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs17124581 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001040437 C6orf48 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4711279 1.06E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001040437 C6orf48 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs9368699 5.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001040437 C6orf48 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs17207629 3.36E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001040437 C6orf48 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs733539 4.64E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001040437 C6orf48 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs733539 5.49E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001040438 C6orf48 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4711279 1.06E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001040438 C6orf48 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs9368699 5.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001040438 C6orf48 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs17207629 3.36E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001040438 C6orf48 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs733539 4.64E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001040438 C6orf48 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs733539 5.49E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001040443 PHF11 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs2031532 5.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001040444 PHF11 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs2031532 5.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001040445 ASB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2878083 4.21E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001040445 ASB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12692245 4.48E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001040445 ASB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9798281 3.87E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001040451 RUFY1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4701136 1.95E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001040452 RUFY1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4701136 1.95E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001040458 ERAP1 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs27524 3.00E-11 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_001040458 ERAP1 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Aminopeptidases rs13160562 7.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_001040458 ERAP1 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs30187 2.00E-27 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_001040458 ERAP1 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs27434 5.00E-12 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_001040610 EFTUD1 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs12324805 7.00E-06 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_001040633 PRKAG2 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs7805747 4.00E-12 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001040633 PRKAG2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs10224002 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001040633 PRKAG2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs10224002 6.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001040633 PRKAG2 21305692 http://www.ncbi.nlm.nih.gov/pubmed/21305692 Bipolar Disorder rs7795096 2.00E-06 Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder. NHGRI|-1
NM_001040647 CRCP 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs875971 4.00E-06 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_001040648 CRCP 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs875971 4.00E-06 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_001040655 TTC23 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs7170952 1.25E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001040656 TTC23 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs7170952 1.25E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001040657 TTC23 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs7170952 1.25E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001040658 TTC23 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs7170952 1.25E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001040659 TTC23 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs7170952 1.25E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001040660 TTC23 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs7170952 1.25E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001040708 HEY1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11997947 9.55E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001040709 SYPL2 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs1933182 1.00E-07 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001040712 PTPRD 18660810 http://www.ncbi.nlm.nih.gov/pubmed/18660810 Restless Legs Syndrome rs1975197 6.00E-09 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. NHGRI|-1
NM_001040712 PTPRD 20174558 http://www.ncbi.nlm.nih.gov/pubmed/20174558 "Diabetes Mellitus, Type 2" rs17584499 9.00E-10 A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. NHGRI|-1
NM_001040712 PTPRD 18660810 http://www.ncbi.nlm.nih.gov/pubmed/18660810 Restless Legs Syndrome rs4626664 6.00E-10 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. NHGRI|-1
NM_001040712 PTPRD 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs2475335 9.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_001040712 PTPRD 21647700 http://www.ncbi.nlm.nih.gov/pubmed/21647700 "Diabetes Mellitus, Type 2" rs649891 6.00E-06 "Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals." NHGRI|-1
NM_001040712 PTPRD 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Braces rs1535480 4.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001040712 PTPRD 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7044355 1.00E-07 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001040712 PTPRD 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10815798 6.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001040875 GDAP1 17903300 http://www.ncbi.nlm.nih.gov/pubmed/17903300 Waist Circumference rs4471028 2.00E-07 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. NHGRI|-1
NM_001040875 GDAP1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Myoglobin rs6472866 8.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001041 SI 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs7427021 5.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001042355 CYLD 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs8060598 3.34E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001042355 CYLD 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs10521222 9.00E-13 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001042376 INS-IGF2 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs3741208 2.00E-07 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_001042376 INS-IGF2 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 "Diabetes Mellitus, Type 1" rs1004446 4.00E-09 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NM_001042376 INS-IGF2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7924316 7.07E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001042383 CEP63 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs10935120 7.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001042384 CEP63 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs10935120 7.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001042400 CEP63 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs10935120 7.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001042412 CYLD 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs8060598 3.34E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001042412 CYLD 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs10521222 9.00E-13 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001042413 GLIS3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10491899 1.52E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001042413 GLIS3 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs7034200 1.00E-12 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001042413 GLIS3 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs7034200 1.00E-13 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001042413 GLIS3 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs7020673 5.00E-12 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001042413 GLIS3 18840781 http://www.ncbi.nlm.nih.gov/pubmed/18840781 "Diabetes Mellitus, Type 1" rs10758593 3.00E-06 Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes. NHGRI|-1
NM_001042429 FAM98B 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs11073328 2.00E-09 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001042432 CLN3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs151181 2.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001042440 CAST 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4434401 6.76E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001042440 CAST 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10053056 2.19E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001042440 CAST 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs27524 3.00E-11 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_001042440 CAST 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9918149 4.77E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001042467 MLPH 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs2292884 4.00E-08 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_001042471 GSDMB 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs2305480 1.00E-07 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_001042471 GSDMB 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs2305480 3.00E-08 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_001042471 GSDMB 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2290400 6.00E-13 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001042471 GSDMB 17611496 http://www.ncbi.nlm.nih.gov/pubmed/17611496 Asthma rs7216389 9.00E-11 Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. NHGRI|-1
NM_001042471 GSDMB 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs2872507 9.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001042471 GSDMB 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2872507 5.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001042471 GSDMB 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2872507 5.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001042471 GSDMB 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs8067378 1.00E-07 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_001042475 C6orf204 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs12210810 2.00E-17 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001042475 C6orf204 19587794 http://www.ncbi.nlm.nih.gov/pubmed/19587794 "Arrhythmias, Cardiac" rs11153730 2.00E-29 Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies. NHGRI|-1
NM_001042475 C6orf204 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11153730 1.00E-18 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001042475 C6orf204 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs11970286 2.00E-24 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001042475 C6orf204 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs11970286 8.00E-07 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001042478 AJAP1 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Height rs7513590 5.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001042478 AJAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4400585 1.58E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001042478 AJAP1 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Factor VII rs966321 8.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001042478 AJAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6679220 1.00E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001042478 AJAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4654432 7.20E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001042478 AJAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4654433 9.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001042481 FRMD6 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs7140150 5.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001042481 FRMD6 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs7153703 3.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001042481 FRMD6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17123958 1.04E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001042482 TPK1 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs10487524 9.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_001042482 TPK1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1468375 1.41E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001042483 NUPR1 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs4788084 3.00E-13 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001042500 DEFA1 21151130 http://www.ncbi.nlm.nih.gov/pubmed/21151130 Endometriosis rs2738113 3.00E-07 Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. NHGRI|-1
NM_001042510 ZNF706 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs1264202 2.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001042510 ZNF706 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3491 1.79E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001042511 ZNF706 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs1264202 2.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001042511 ZNF706 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3491 1.79E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001042517 DIAPH3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs7336489 8.33E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001042517 DIAPH3 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs10492604 4.00E-06 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_001042517 DIAPH3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7988007 6.28E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001042517 DIAPH3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs9538078 7.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001042517 DIAPH3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1330748 1.01E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001042517 DIAPH3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs1537473 7.53E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001042517 DIAPH3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs9569918 7.11E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001042517 DIAPH3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12428128 1.19E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001042517 DIAPH3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12428128 2.02E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001042536 INSC 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7117858 6.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001042536 INSC 21104366 http://www.ncbi.nlm.nih.gov/pubmed/21104366 Bone Density rs11023787 5.00E-16 A genome-wide association analysis implicates SOX6 as a candidate gene for wrist bone mass. NHGRI|-1
NM_001042543 GLRA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6824735 3.90E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001042550 SMC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1867347 2.08E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001042551 SMC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1867347 2.08E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001042555 FRS2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs10748128 2.00E-20 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001042555 FRS2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs11177669 3.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001042574 CRTC3 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs12915189 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001042583 CD1E 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1065457 6.43E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001042584 CD1E 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1065457 6.43E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001042585 CD1E 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1065457 6.43E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001042586 CD1E 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1065457 6.43E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001042587 CD1E 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1065457 6.43E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001042599 ERBB4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1851196 5.11E-06 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001042599 ERBB4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs839511 2.58E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001042599 ERBB4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs16849204 3.22E-05 NBL-GWAS version 2 dbGaP|2895
NM_001042599 ERBB4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7600221 6.53E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001042599 ERBB4 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Eosinophils rs12619285 5.00E-10 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_001042610 DBNDD1 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs11648785 3.00E-09 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_001042625 CAPSL 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs1445898 8.00E-06 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_001042625 CAPSL 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs860413 1.00E-11 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001042625 CAPSL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2194225 6.57E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001042635 NGDN 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs223116 3.00E-08 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_001042669 ARHGAP24 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs7692808 6.00E-20 Genome-wide association study of PR interval. NHGRI|-1
NM_001042669 ARHGAP24 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs7660702 3.00E-17 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001042669 ARHGAP24 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs345328 2.91E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001042681 RERE 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs4908760 7.00E-15 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_001042681 RERE 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs12025126 6.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_001042682 RERE 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs4908760 7.00E-15 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_001042682 RERE 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs12025126 6.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_001042692 C2orf86 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Interleukin-6 rs11683229 6.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001042724 PVRL2 20885792 http://www.ncbi.nlm.nih.gov/pubmed/20885792 Alzheimer Disease rs6859 1.00E-07 Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. NHGRI|-1
NM_001042724 PVRL2 18823527 http://www.ncbi.nlm.nih.gov/pubmed/18823527 Alzheimer Disease rs6859 6.00E-14 A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. NHGRI|-1
NM_001042749 STAG2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs5910058 9.96E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001042750 STAG2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs5910058 9.96E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001042751 STAG2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs5910058 9.96E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001042758 SRGAP2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2336938 2.83E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001042762 FIGNL1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs12718597 5.00E-13 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001042780 TNNT3 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs909116 7.00E-07 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001042781 TNNT3 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs909116 7.00E-07 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001042782 TNNT3 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs909116 7.00E-07 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001044390 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001044390 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001044391 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001044391 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001044392 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001044392 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001046 SLC12A2 21139019 http://www.ncbi.nlm.nih.gov/pubmed/21139019 Carcinoid Tumor rs10089 2.00E-06 A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum. NHGRI|-1
NM_001048209 NTM 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs1550976 3.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_001048209 NTM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs1550976 5.59E-06 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_001048209 NTM 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs992564 4.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001048230 ADORA1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs16851020 4.14E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001048252 CTXN3 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs245201 9.00E-08 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_001048252 CTXN3 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs374499 8.86E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001050 SSTR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1037260 6.50E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001051 SSTR3 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs229541 2.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001051 SSTR3 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs229541 2.00E-08 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_001059 TACR3 19483681 http://www.ncbi.nlm.nih.gov/pubmed/19483681 Testicular Neoplasms rs4699052 2.00E-07 A genome-wide association study of testicular germ cell tumor. NHGRI|-1
NM_001062 TCN1 19303062 http://www.ncbi.nlm.nih.gov/pubmed/19303062 Vitamin B 12 rs526934 2.00E-06 "Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations." NHGRI|-1
NM_001063 TF 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1799852 5.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001063 TF 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs1799899 1.00E-09 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_001063 TF 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs3811647 1.00E-35 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_001063 TF 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs3811647 3.00E-47 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_001063 TF 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs3811647 3.00E-15 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001063 TF 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs1049296 5.00E-43 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_001063 TF 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1830084 1.00E-09 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001064 TKT 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs4687718 6.00E-09 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001065 TNFRSF1A 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs1800693 2.00E-09 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001065 TNFRSF1A 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs1800693 2.00E-11 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_001065 TNFRSF1A 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs4149584 5.00E-06 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_001072 UGT1A6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1604144 4.75E-05 NBL-GWAS version 2 dbGaP|2895
NM_001072 UGT1A6 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs887829 1.00E-69 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_001072 UGT1A6 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs6742078 5E-324 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_001072 UGT1A6 21646302 http://www.ncbi.nlm.nih.gov/pubmed/21646302 Bilirubin rs4148325 5.00E-62 Mayo genome consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. NHGRI|-1
NM_001075099 SKAP1 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs2084881 2.00E-06 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_001075099 SKAP1 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs9303542 1.00E-06 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_001076678 ZNF493 19207018 http://www.ncbi.nlm.nih.gov/pubmed/19207018 Pain Measurement rs2562456 2.00E-10 Genome-wide association study of acute post-surgical pain in humans. NHGRI|-1
NM_001076682 NCAM1 21212386 http://www.ncbi.nlm.nih.gov/pubmed/21212386 Blood Vessels rs1436109 3.00E-07 Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. NHGRI|-1
NM_001076682 NCAM1 21212386 http://www.ncbi.nlm.nih.gov/pubmed/21212386 Blood Vessels rs1436109 4.00E-09 Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. NHGRI|-1
NM_001076682 NCAM1 21212386 http://www.ncbi.nlm.nih.gov/pubmed/21212386 Blood Vessels rs1436109 9.00E-07 Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. NHGRI|-1
NM_001076682 NCAM1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs12279261 9.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001076682 NCAM1 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs7105881 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001076778 FAM107A 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs13315591 5.00E-08 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001076780 PKD1L2 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs4889240 7.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001076780 PKD1L2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9931907 1.18E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001076780 PKD1L2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs8060294 9.40E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001076780 PKD1L2 19185284 http://www.ncbi.nlm.nih.gov/pubmed/19185284 beta Carotene rs6564851 2.00E-24 "Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study." NHGRI|-1
NM_001076786 QSER1 19772629 http://www.ncbi.nlm.nih.gov/pubmed/19772629 Parkinson Disease rs10767971 5.00E-07 Genomewide association study for onset age in Parkinson disease. NHGRI|-1
NM_001076787 TP53I11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7121790 1.34E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001077183 TSC2 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs2516739 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001077188 HS6ST2 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs17324272 2.00E-07 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001077243 GRIA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10895889 7.40E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001077244 GRIA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10895889 7.40E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001077261 NCOR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7956328 6.36E-06 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001077261 NCOR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7956328 8.55E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001077394 DPH5 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs17410015 2.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001077395 DPH5 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs17410015 2.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001077397 IRF2BP2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs744487 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001077442 HNRNPC 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8016099 3.74E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001077442 HNRNPC 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs17197037 2.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_001077443 HNRNPC 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8016099 3.74E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001077443 HNRNPC 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs17197037 2.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_001077484 SLC38A1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs1373549 8.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_001077488 GNAS 21046636 http://www.ncbi.nlm.nih.gov/pubmed/21046636 Brain Waves rs13831 6.00E-06 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. NHGRI|-1
NM_001077489 GNAS 21046636 http://www.ncbi.nlm.nih.gov/pubmed/21046636 Brain Waves rs13831 6.00E-06 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. NHGRI|-1
NM_001077490 GNAS 21046636 http://www.ncbi.nlm.nih.gov/pubmed/21046636 Brain Waves rs13831 6.00E-06 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. NHGRI|-1
NM_001077511 TCF19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3130453 2.06E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001077511 TCF19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3094187 3.73E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001077511 TCF19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7750641 5.60E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001077511 TCF19 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs7750641 7.36E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001077511 TCF19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9263794 9.83E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001077511 TCF19 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2073723 5.10E-08 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001077523 AP3D1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Mass Index rs3803915 5.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001077594 C14orf73 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs8017161 3.00E-13 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001077624 ZNF846 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2112837 5.59E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001077653 TBX20 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs1362212 1.00E-13 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001077653 TBX20 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs2392362 2.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001077653 TBX20 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Liver Cirrhosis rs343064 3.00E-08 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001077653 TBX20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs74992754 6.07E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001077685 AGAP7 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs3123078 1.00E-19 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001077710 FAM110C 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs11542478 9.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001077710 FAM110C 21423239 http://www.ncbi.nlm.nih.gov/pubmed/21423239 "Suicide, Attempted" rs300774 5.00E-08 A genome-wide association study of attempted suicide. NHGRI|-1
NM_001078170 RGPD2 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs12714207 5.00E-07 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_001078650 TMEM134 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7124630 4.90E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001078651 TMEM134 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7124630 4.90E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001079515 TBCE 19557161 http://www.ncbi.nlm.nih.gov/pubmed/19557161 Adiposity rs6429082 3.00E-07 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. NHGRI|-1
NM_001079520 DACT1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10150529 1.49E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001079526 IKZF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs16849204 3.22E-05 NBL-GWAS version 2 dbGaP|2895
NM_001079526 IKZF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7600221 6.53E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001079526 IKZF2 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Eosinophils rs12619285 5.00E-10 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_001079533 CPEB1 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs783540 4.00E-06 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_001079534 CPEB1 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs783540 4.00E-06 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_001079535 CPEB1 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs783540 4.00E-06 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_001079668 NKX2-1 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs17104630 8.00E-06 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001079670 CAB39L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7328100 8.21E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001079684 KIAA1191 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3749804 3.54E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001079684 KIAA1191 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11134974 4.26E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001079684 KIAA1191 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10063877 3.75E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001079685 KIAA1191 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3749804 3.54E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001079685 KIAA1191 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11134974 4.26E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001079685 KIAA1191 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10063877 3.75E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001079810 XIRP2 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs13015447 7.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001079811 GLB1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs13314993 3.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001079811 GLB1 21105107 http://www.ncbi.nlm.nih.gov/pubmed/21105107 "Carcinoma, Hepatocellular" rs4678680 2.00E-07 Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma. NHGRI|-1
NM_001079817 INSR 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs2115386 3.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001079818 ITGA6 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs12621278 9.00E-23 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001079821 NLRP3 20031576 http://www.ncbi.nlm.nih.gov/pubmed/20031576 Fibrinogen rs1539019 1.00E-08 Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. NHGRI|-1
NM_001079821 NLRP3 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs12239046 1.00E-15 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001079821 NLRP3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10399826 2.06E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001079821 NLRP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11802371 1.11E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001079823 LAMA2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs17799083 1.88E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001079843 CASZ1 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs880315 3.00E-10 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_001079843 CASZ1 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs880315 7.00E-07 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_001079843 CASZ1 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs12046278 5.00E-06 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001079843 CASZ1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1280975 4.93E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001079858 GPR64 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs5955711 9.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001079859 GPR64 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs5955711 9.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001079860 GPR64 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs5955711 9.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001079867 PEX2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7821178 3.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001079867 PEX2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs7846385 5.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001079867 PEX2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs3864663 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001079867 PEX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10091852 8.64E-05 NBL-GWAS version 2 dbGaP|2895
NM_001079878 CNGA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7571001 1.95E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001079880 PRKD2 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs11083846 4.00E-09 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NM_001079880 PRKD2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs425105 3.00E-11 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001079881 PRKD2 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs11083846 4.00E-09 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NM_001079881 PRKD2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs425105 3.00E-11 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001079882 PRKD2 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs11083846 4.00E-09 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NM_001079882 PRKD2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs425105 3.00E-11 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001080121 PRNP 19081515 http://www.ncbi.nlm.nih.gov/pubmed/19081515 Creutzfeldt-Jakob Syndrome rs1799990 2.00E-21 Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. NHGRI|-1
NM_001080121 PRNP 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs6052699 2.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001080122 PRNP 19081515 http://www.ncbi.nlm.nih.gov/pubmed/19081515 Creutzfeldt-Jakob Syndrome rs1799990 2.00E-21 Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. NHGRI|-1
NM_001080122 PRNP 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs6052699 2.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001080123 PRNP 19081515 http://www.ncbi.nlm.nih.gov/pubmed/19081515 Creutzfeldt-Jakob Syndrome rs1799990 2.00E-21 Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. NHGRI|-1
NM_001080123 PRNP 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs6052699 2.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001080209 TMEM200C 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4798376 7.57E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001080209 TMEM200C 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11662763 5.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_001080378 PACRG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2206256 1.04E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001080378 PACRG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs11966842 2.88E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001080378 PACRG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs11966948 1.12E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001080378 PACRG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6904305 2.32E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001080379 PACRG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2206256 1.04E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001080379 PACRG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs11966842 2.88E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001080379 PACRG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs11966948 1.12E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001080379 PACRG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6904305 2.32E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001080395 AATK 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs7225354 9.76E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001080396 FAM155A 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs957788 8.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_001080396 FAM155A 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10492664 1.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001080396 FAM155A 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs1927745 5.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_001080408 PROX2 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs8014204 5.00E-06 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_001080411 ZNF433 20598377 http://www.ncbi.nlm.nih.gov/pubmed/20598377 Multiple Sclerosis rs3745672 1.00E-06 Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. NHGRI|-1
NM_001080412 ZBTB38 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs6440003 2.00E-24 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001080412 ZBTB38 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs6763931 1.00E-27 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001080412 ZBTB38 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs6763931 3.00E-12 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001080412 ZBTB38 18193045 http://www.ncbi.nlm.nih.gov/pubmed/18193045 Body Height rs724016 1.00E-06 Common variants in the GDF5-UQCC region are associated with variation in human height. NHGRI|-1
NM_001080412 ZBTB38 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs724016 8.00E-22 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001080412 ZBTB38 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs9825379 6.00E-09 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001080412 ZBTB38 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Body Height rs10513137 6.00E-12 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001080412 ZBTB38 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs10513137 8.00E-08 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001080420 SHANK3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs9616906 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001080421 UNC13A 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs12608932 3.00E-14 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001080426 DUSP27 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs869714 1.54E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001080426 DUSP27 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7527143 2.65E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001080427 THSD7B 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs934299 9.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_001080427 THSD7B 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs1427593 7.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_001080430 TOX3 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs3803662 1.00E-36 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_001080430 TOX3 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs3803662 1.00E-09 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_001080430 TOX3 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs3803662 3.00E-15 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001080430 TOX3 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs3803662 4.00E-07 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_001080430 TOX3 17529974 http://www.ncbi.nlm.nih.gov/pubmed/17529974 Breast Neoplasms rs3803662 6.00E-19 Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer. NHGRI|-1
NM_001080430 TOX3 20585626 http://www.ncbi.nlm.nih.gov/pubmed/20585626 Breast Neoplasms rs4784227 1.00E-28 Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium. NHGRI|-1
NM_001080430 TOX3 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs3112612 4.00E-10 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_001080430 TOX3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3104807 1.01E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001080430 TOX3 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Exploratory Behavior rs4131099 4.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_001080430 TOX3 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1362756 5.00E-09 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_001080431 SLC45A4 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs7386474 3.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001080432 FTO 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6499640 4.00E-13 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001080432 FTO 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6499640 6.00E-14 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001080432 FTO 19151714 http://www.ncbi.nlm.nih.gov/pubmed/19151714 Obesity rs1421085 1.00E-28 Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. NHGRI|-1
NM_001080432 FTO 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs1558902 5.00E-120 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001080432 FTO 21544081 http://www.ncbi.nlm.nih.gov/pubmed/21544081 Obesity rs1558902 1.00E-07 "Replication of 13 obesity loci among Singaporean Chinese, Malay and Asian-Indian populations." NHGRI|-1
NM_001080432 FTO 20421936 http://www.ncbi.nlm.nih.gov/pubmed/20421936 Obesity rs1558902 7.00E-13 Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups. NHGRI|-1
NM_001080432 FTO 19557197 http://www.ncbi.nlm.nih.gov/pubmed/19557197 Waist Circumference rs1558902 5.00E-19 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. NHGRI|-1
NM_001080432 FTO 18454148 http://www.ncbi.nlm.nih.gov/pubmed/18454148 Body Mass Index rs1121980 4.00E-08 "Common variants near MC4R are associated with fat mass, weight and risk of obesity." NHGRI|-1
NM_001080432 FTO 18159244 http://www.ncbi.nlm.nih.gov/pubmed/18159244 Obesity rs1121980 1.00E-07 Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants. NHGRI|-1
NM_001080432 FTO 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17817449 2.00E-12 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001080432 FTO 21706003 http://www.ncbi.nlm.nih.gov/pubmed/21706003 Adiposity rs8050136 3.00E-26 Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile. NHGRI|-1
NM_001080432 FTO 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs8050136 1.00E-47 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001080432 FTO 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs8050136 5.00E-36 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001080432 FTO 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs8050136 1.00E-12 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001080432 FTO 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs8050136 2.00E-17 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001080432 FTO 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs8050136 7.00E-14 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001080432 FTO 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs8050136 7.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001080432 FTO 21037115 http://www.ncbi.nlm.nih.gov/pubmed/21037115 Obesity rs8050136 4.00E-08 Genome-Wide Association Analysis of Body Mass in Chronic Obstructive Pulmonary Disease. NHGRI|-1
NM_001080432 FTO 17434869 http://www.ncbi.nlm.nih.gov/pubmed/17434869 Body Mass Index rs9939609 2.00E-20 A common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesity. NHGRI|-1
NM_001080432 FTO 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Body Mass Index rs9939609 2.00E-07 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001080432 FTO 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs9939609 4.00E-51 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_001080432 FTO 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs9939609 2.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001080432 FTO 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs9939609 3.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001080432 FTO 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs9941349 6.00E-12 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_001080432 FTO 17658951 http://www.ncbi.nlm.nih.gov/pubmed/17658951 Body Mass Index rs9930506 9.00E-07 Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. NHGRI|-1
NM_001080432 FTO 17658951 http://www.ncbi.nlm.nih.gov/pubmed/17658951 Waist-Hip Ratio rs9930506 3.00E-08 Genome-wide association scan shows genetic variants in the FTO gene are associated with obesity-related traits. NHGRI|-1
NM_001080432 FTO 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs11642841 3.00E-08 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001080433 CCDC85A 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs17268785 1.00E-10 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001080433 CCDC85A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1468958 8.06E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001080433 CCDC85A 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs6751715 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001080440 OTOL1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs6808138 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001080440 OTOL1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Behavior rs6808138 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001080444 IGSF5 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs1735151 9.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001080444 IGSF5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2837170 1.32E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001080444 IGSF5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2837170 2.39E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001080448 EPHA6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1825828 1.82E-07 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001080452 GPR108 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs171094 1.39E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001080455 SLC35F4 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Bipolar Disorder rs10134944 7.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001080455 SLC35F4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1092015 2.23E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001080455 SLC35F4 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs8013190 7.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001080455 SLC35F4 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs1335515 8.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_001080455 SLC35F4 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Maximal Midexpiratory Flow Rate rs808225 7.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_001080455 SLC35F4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2747100 1.13E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001080458 EVX2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs847126 6.56E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001080463 DYNC2H1 21118971 http://www.ncbi.nlm.nih.gov/pubmed/21118971 Small Cell Lung Carcinoma rs716274 9.00E-08 Genome-wide interrogation identifies YAP1 variants associated with survival of small-cell lung cancer patients. NHGRI|-1
NM_001080463 DYNC2H1 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs1917445 6.00E-07 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001080463 DYNC2H1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs974819 2.00E-09 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_001080467 MYO5B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1705533 6.07E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001080471 PEAR1 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs12566888 4.00E-16 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001080471 PEAR1 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs12566888 5.00E-19 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001080473 MFSD2B 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 C-Reactive Protein rs7561273 6.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001080476 GRXCR1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs4861040 2.00E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001080476 GRXCR1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1074454 2.00E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001080476 GRXCR1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1074453 2.00E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001080479 RGNEF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs6869486 4.61E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001080479 RGNEF 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs16871023 1.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001080480 MBOAT1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1202199 9.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001080491 USP6NL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7085769 1.11E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001080491 USP6NL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs4445554 7.16E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001080491 USP6NL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs10508425 1.56E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001080509 TSPAN11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3741869 3.19E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001080511 CLEC2L 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs10954654 2.79E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001080515 FAM163B 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs3025343 4.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001080520 DRGX 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs4838508 2.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001080522 CC2D2A 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1861050 8.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001080529 WIPF3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs850084 2.86E-09 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001080532 TMC3 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4778944 9.28E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001080534 UNC13C 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs1897031 1.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001080534 UNC13C 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Alkaline Phosphatase rs10518765 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001080534 UNC13C 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10518765 2.19E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001080534 UNC13C 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs16976033 7.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001080538 AKR1B15 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4732038 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001080546 TMEM218 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs585977 6.15E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001080744 DGKG 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs7647305 7.00E-11 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001080744 DGKG 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7647305 4.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001080744 DGKG 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs9816226 2.00E-18 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001080745 DGKG 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs7647305 7.00E-11 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001080745 DGKG 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7647305 4.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001080745 DGKG 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs9816226 2.00E-18 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001080997 RTBDN 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7255045 2.00E-12 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001081 CUBN 21355061 http://www.ncbi.nlm.nih.gov/pubmed/21355061 Albuminuria rs1801239 1.00E-11 CUBN is a gene locus for albuminuria. NHGRI|-1
NM_001081 CUBN 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Blood Pressure rs10508517 6.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001081 CUBN 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs12246329 2.06E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001081 CUBN 19303062 http://www.ncbi.nlm.nih.gov/pubmed/19303062 Vitamin B 12 rs11254363 1.00E-06 "Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations." NHGRI|-1
NM_001081 CUBN 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs6602175 3.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001081573 GAB3 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2664170 8.00E-09 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001081676 SCN3A 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Foot rs776488 2.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001081677 SCN3A 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Foot rs776488 2.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001081686 G6PC2 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs1402837 5.00E-10 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_001081686 G6PC2 19060907 http://www.ncbi.nlm.nih.gov/pubmed/19060907 Blood Glucose rs560887 1.00E-57 Variants in MTNR1B influence fasting glucose levels. NHGRI|-1
NM_001081686 G6PC2 18451265 http://www.ncbi.nlm.nih.gov/pubmed/18451265 Blood Glucose rs560887 4.00E-23 A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels. NHGRI|-1
NM_001081686 G6PC2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs560887 9.00E-218 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001081686 G6PC2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs560887 2.00E-66 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001081686 G6PC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs560887 5.69E-10 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_001081686 G6PC2 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Glucose rs560887 6.00E-10 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001081686 G6PC2 18521185 http://www.ncbi.nlm.nih.gov/pubmed/18521185 Blood Glucose rs563694 4.00E-07 Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels. NHGRI|-1
NM_001081686 G6PC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs563694 1.17E-07 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_001081955 RGS9 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs8068707 2.40E-06 NBL-GWAS version 1 dbGaP|2845
NM_001081976 ADORA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10857899 3.06E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001081976 ADORA3 20548944 http://www.ncbi.nlm.nih.gov/pubmed/20548944 Bone Density rs494453 4.00E-08 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. NHGRI|-1
NM_001082 CYP4F2 19578179 http://www.ncbi.nlm.nih.gov/pubmed/19578179 Acenocoumarol rs2108622 3.00E-10 A genome-wide association study of acenocoumarol maintenance dosage. NHGRI|-1
NM_001082 CYP4F2 21729881 http://www.ncbi.nlm.nih.gov/pubmed/21729881 Vitamin E rs2108622 1.00E-10 Genome-wide association study identifies common variants associated with circulating vitamin E levels NHGRI|-1
NM_001082 CYP4F2 19300499 http://www.ncbi.nlm.nih.gov/pubmed/19300499 Warfarin rs2108622 3.00E-10 "A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose." NHGRI|-1
NM_001082 CYP4F2 20833655 http://www.ncbi.nlm.nih.gov/pubmed/20833655 Warfarin rs2108622 3.00E-08 Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. NHGRI|-1
NM_001082533 CA10 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs8073783 8.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001082533 CA10 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs9635759 7.00E-13 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001082534 CA10 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs8073783 8.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001082534 CA10 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs9635759 7.00E-13 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001082575 RBFOX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs898528 4.94E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001082618 CD33 18976728 http://www.ncbi.nlm.nih.gov/pubmed/18976728 Alzheimer Disease rs3826656 6.00E-06 Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE. NHGRI|-1
NM_001082618 CD33 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs3865444 2.00E-09 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_001082959 SCARB1 21729881 http://www.ncbi.nlm.nih.gov/pubmed/21729881 Vitamin E rs11057830 8.00E-09 Genome-wide association study identifies common variants associated with circulating vitamin E levels NHGRI|-1
NM_001082959 SCARB1 20442857 http://www.ncbi.nlm.nih.gov/pubmed/20442857 1-Alkyl-2-acetylglycerophosphocholine Esterase rs10846744 1.00E-08 Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study. NHGRI|-1
NM_001082959 SCARB1 21131975 http://www.ncbi.nlm.nih.gov/pubmed/21131975 "Carcinoma, Renal Cell" rs4765623 3.00E-08 Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3. NHGRI|-1
NM_001082959 SCARB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7956328 6.36E-06 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001082959 SCARB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7956328 8.55E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001082967 FAM19A5 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs130110 4.58E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001082967 FAM19A5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs78492 4.91E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001082967 FAM19A5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11090762 9.31E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001082967 FAM19A5 18821564 http://www.ncbi.nlm.nih.gov/pubmed/18821564 Attention Deficit Disorder with Hyperactivity rs9627183 3.00E-06 Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder. NHGRI|-1
NM_001082971 DDC 19465909 http://www.ncbi.nlm.nih.gov/pubmed/19465909 Malaria rs1451375 6.00E-06 Genome-wide and fine-resolution association analysis of malaria in West Africa. NHGRI|-1
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12510138 7.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1383532 6.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6534139 4.40E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6835635 3.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs13128602 3.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1552095 3.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1010740 3.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs3736115 2.10E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17050695 5.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs1845344 7.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11098524 7.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9993199 9.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2389803 1.12E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1480931 1.11E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10518329 1.12E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10006706 6.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6849561 7.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12508504 9.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001083112 GPD2 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs7601713 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001083113 ZGPAT 18758464 http://www.ncbi.nlm.nih.gov/pubmed/18758464 Inflammatory Bowel Diseases rs2315008 9.00E-15 Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. NHGRI|-1
NM_001083113 ZGPAT 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs4809330 3.00E-15 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001083116 PRF1 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs10999409 5.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_001083308 PYDC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6444558 1.54E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001083308 PYDC2 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7635839 3.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001083335 ZFP112 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2609881 5.38E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001083591 CELF2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs3780993 6.86E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001083591 CELF2 21379329 http://www.ncbi.nlm.nih.gov/pubmed/21379329 Alzheimer Disease rs62209 2.00E-07 Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE. NHGRI|-1
NM_001083592 ROR1 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs2749097 2.00E-09 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_001083592 ROR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11208285 9.59E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001083592 ROR1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2819130 1.23E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001083602 PTCH1 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs16909898 5.00E-07 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001083602 PTCH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs10512248 4.00E-11 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001083602 PTCH1 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs10988802 4.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NM_001083603 PTCH1 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs16909898 5.00E-07 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001083603 PTCH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs10512248 4.00E-11 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001083603 PTCH1 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs10988802 4.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NM_001083604 PTCH1 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs16909898 5.00E-07 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001083604 PTCH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs10512248 4.00E-11 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001083604 PTCH1 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs10988802 4.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NM_001083605 PTCH1 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs16909898 5.00E-07 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001083605 PTCH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs10512248 4.00E-11 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001083605 PTCH1 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs10988802 4.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NM_001083606 PTCH1 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs16909898 5.00E-07 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001083606 PTCH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs10512248 4.00E-11 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001083606 PTCH1 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs10988802 4.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NM_001083607 PTCH1 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs16909898 5.00E-07 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001083607 PTCH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs10512248 4.00E-11 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001083607 PTCH1 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs10988802 4.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NM_001083612 AGPHD1 18780872 http://www.ncbi.nlm.nih.gov/pubmed/18780872 Lung Neoplasms rs8034191 1.00E-08 Familial aggregation of common sequence variants on 15q24-25.1 in lung cancer. NHGRI|-1
NM_001083612 AGPHD1 18385676 http://www.ncbi.nlm.nih.gov/pubmed/18385676 Lung Neoplasms rs8034191 3.00E-18 Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. NHGRI|-1
NM_001083612 AGPHD1 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs8034191 3.00E-26 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_001083612 AGPHD1 18385738 http://www.ncbi.nlm.nih.gov/pubmed/18385738 Lung Neoplasms rs8034191 5.00E-20 A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25. NHGRI|-1
NM_001083612 AGPHD1 19300482 http://www.ncbi.nlm.nih.gov/pubmed/19300482 "Pulmonary Disease, Chronic Obstructive" rs8034191 1.00E-10 A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci. NHGRI|-1
NM_001083612 AGPHD1 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs28675338 1.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001083621 ZBTB40 20601957 http://www.ncbi.nlm.nih.gov/pubmed/20601957 Endometriosis rs16826658 2.00E-06 A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese. NHGRI|-1
NM_001083621 ZBTB40 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs7521902 5.00E-06 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_001083621 ZBTB40 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs7524102 1.00E-16 New sequence variants associated with bone mineral density. NHGRI|-1
NM_001083621 ZBTB40 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs7524102 1.00E-06 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_001083621 ZBTB40 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7524102 3.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001083621 ZBTB40 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs7524102 5.00E-16 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_001083621 ZBTB40 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs7524102 9.00E-07 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_001083621 ZBTB40 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs7524102 9.00E-09 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_001083621 ZBTB40 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs7524102 2.00E-13 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001083621 ZBTB40 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs7524102 3.00E-07 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_001083621 ZBTB40 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs6696981 2.00E-08 New sequence variants associated with bone mineral density. NHGRI|-1
NM_001083621 ZBTB40 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs6426749 9.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001083625 ANKRD12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1114591 3.23E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001083899 GP6 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs1671152 8.00E-14 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001083907 BANK1 18204447 http://www.ncbi.nlm.nih.gov/pubmed/18204447 "Lupus Erythematosus, Systemic" rs10516487 4.00E-10 Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus. NHGRI|-1
NM_001083907 BANK1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7694392 4.26E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001083907 BANK1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4640677 6.62E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001083907 BANK1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs12648641 9.89E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001083914 CTBP2 18264096 http://www.ncbi.nlm.nih.gov/pubmed/18264096 Prostatic Neoplasms rs4962416 2.00E-07 Multiple loci identified in a genome-wide association study of prostate cancer. NHGRI|-1
NM_001083953 THADA 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs7590268 9.00E-08 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_001083953 THADA 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs1465618 2.00E-08 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001083953 THADA 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs6732426 1.00E-07 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001083953 THADA 21151128 http://www.ncbi.nlm.nih.gov/pubmed/21151128 Polycystic Ovary Syndrome rs13429458 2.00E-23 "Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3." NHGRI|-1
NM_001083953 THADA 21151128 http://www.ncbi.nlm.nih.gov/pubmed/21151128 Polycystic Ovary Syndrome rs12478601 3.00E-23 "Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3." NHGRI|-1
NM_001083953 THADA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7578597 1.00E-09 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001083953 THADA 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs10495903 2.00E-14 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001083956 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Anthropometry rs7792939 5.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001083956 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weight rs7792939 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001083956 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weights and Measures rs7792939 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001083962 TCF4 19571811 http://www.ncbi.nlm.nih.gov/pubmed/19571811 Schizophrenia rs17594526 1.00E-07 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. NHGRI|-1
NM_001083962 TCF4 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs9960767 4.00E-09 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_001083962 TCF4 20825314 http://www.ncbi.nlm.nih.gov/pubmed/20825314 Fuchs Endothelial Dystrophy rs613872 1.00E-18 E2-2 protein and Fuchs's corneal dystrophy. NHGRI|-1
NM_001083962 TCF4 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs1970671 3.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001085049 MRAS 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs2306374 3.00E-08 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001085049 MRAS 19198612 http://www.ncbi.nlm.nih.gov/pubmed/19198612 Coronary Artery Disease rs9818870 7.00E-13 New susceptibility locus for coronary artery disease on chromosome 3q22.3. NHGRI|-1
NM_001085357 BTLA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2633580 3.66E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001085357 BTLA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2633578 3.53E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001085366 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Anthropometry rs7792939 5.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001085366 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weight rs7792939 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001085366 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weights and Measures rs7792939 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001085367 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Anthropometry rs7792939 5.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001085367 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weight rs7792939 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001085367 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weights and Measures rs7792939 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001085368 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Anthropometry rs7792939 5.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001085368 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weight rs7792939 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001085368 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weights and Measures rs7792939 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001085377 MCC 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs1318772 1.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_001085420 PLSCR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2868452 3.18E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001085423 C17orf60 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs6504218 1.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_001085425 ARSA 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs9616906 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001085426 ARSA 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs9616906 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001085427 ARSA 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs9616906 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001085428 ARSA 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs9616906 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001085429 TMEM213 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6969815 1.36E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001085429 TMEM213 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12670097 2.85E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001085429 TMEM213 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12670097 9.68E-06 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001085430 C17orf67 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs227731 1.00E-08 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_001085430 C17orf67 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs4794665 1.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001085480 FAM162B 21460395 http://www.ncbi.nlm.nih.gov/pubmed/21460395 Telomere length rs654128 3.00E-06 A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer. NHGRI|-1
NM_001085481 MAP1LC3B2 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs2089222 8.00E-08 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001085487 MYSM1 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs2811893 3.00E-07 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_001086 AADAC 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs6798928 3.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_001090 ABCF1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3132610 1.15E-08 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001091 ABP1 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs2968864 8.00E-16 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001091 ABP1 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs2968863 2.00E-15 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001091 ABP1 20062061 http://www.ncbi.nlm.nih.gov/pubmed/20062061 Electrocardiography rs4725982 3.00E-06 Genetic variation in SCN10A influences cardiac conduction. NHGRI|-1
NM_001091 ABP1 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs4725982 5.00E-16 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001093772 KIT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11732323 5.78E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001093772 KIT 18193045 http://www.ncbi.nlm.nih.gov/pubmed/18193045 Body Height rs17690232 4.00E-07 Common variants in the GDF5-UQCC region are associated with variation in human height. NHGRI|-1
NM_001093772 KIT 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Count rs218237 2.00E-17 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001093772 KIT 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs218237 3.00E-25 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001093772 KIT 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs172629 1.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001093772 KIT 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs2537859 4.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001094 ACCN1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs11650066 6.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_001097633 GCNT1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs6560517 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001097634 GCNT1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs6560517 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001097635 GCNT1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs6560517 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001097636 GCNT1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs6560517 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001097638 FUT2 18776911 http://www.ncbi.nlm.nih.gov/pubmed/18776911 Vitamin B 12 rs492602 5.00E-17 Common variants of FUT2 are associated with plasma vitamin B12 levels. NHGRI|-1
NM_001097638 FUT2 19303062 http://www.ncbi.nlm.nih.gov/pubmed/19303062 Vitamin B 12 rs602662 3.00E-20 "Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations." NHGRI|-1
NM_001097638 FUT2 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs504963 2.00E-08 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_001097638 FUT2 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs281379 7.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001098169 BSX 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs6589964 2.00E-12 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001098268 LIG4 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10492664 1.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001098478 HLA-F 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1362126 7.54E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001098479 HLA-F 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1362126 7.54E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001098482 CRTC1 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs10423674 6.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001098486 SLC17A3 18834626 http://www.ncbi.nlm.nih.gov/pubmed/18834626 Uric Acid rs1165205 4.00E-29 Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study. NHGRI|-1
NM_001098486 SLC17A3 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs1408272 1.00E-11 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001098486 SLC17A3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1408272 4.00E-39 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001098486 SLC17A3 21149283 http://www.ncbi.nlm.nih.gov/pubmed/21149283 Iron-Regulatory Proteins rs1408272 9.00E-09 Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. NHGRI|-1
NM_001098500 KIAA1217 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 "Ear, External" rs11013962 3.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001098500 KIAA1217 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11014058 6.43E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001098503 PTPRJ 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs11039571 9.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001098506 CEACAM21 21682944 http://www.ncbi.nlm.nih.gov/pubmed/21682944 Schizophrenia rs4803480 1.00E-07 DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population. NHGRI|-1
NM_001098510 PELI3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1791682 1.08E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001098511 KIF2A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2030889 6.48E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001098511 KIF2A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6449558 7.12E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001098512 PRKG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7080306 9.57E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001098517 CADM1 17903292 http://www.ncbi.nlm.nih.gov/pubmed/17903292 Albumins rs1712790 2.00E-06 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001098533 CDK10 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs258322 2.00E-23 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_001098533 CDK10 19578364 http://www.ncbi.nlm.nih.gov/pubmed/19578364 Melanoma rs258322 3.00E-27 Genome-wide association study identifies three loci associated with melanoma risk. NHGRI|-1
NM_001098534 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1077393 3.83E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001098534 BAT3 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs760293 9.72E-20 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001098534 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs805303 2.79E-119 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001098534 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs805303 1.25E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001098534 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3130050 1.52E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001098534 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3117583 3.33E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001098534 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3117582 2.62E-83 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001098534 BAT3 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs3117582 4.00E-10 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_001098534 BAT3 18978787 http://www.ncbi.nlm.nih.gov/pubmed/18978787 Lung Neoplasms rs3117582 5.00E-10 Common 5p15.33 and 6p21.33 variants influence lung cancer risk. NHGRI|-1
NM_001098534 BAT3 19836008 http://www.ncbi.nlm.nih.gov/pubmed/19836008 Lung Neoplasms rs3117582 5.00E-12 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. NHGRI|-1
NM_001098534 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3117582 4.53E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001098579 MRVI1 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7940646 1.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001098579 MRVI1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2018368 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001098579 MRVI1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11042937 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001098623 OBSCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs435776 5.30E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001098624 MID1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs5934953 1.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001098624 MID1 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs12388359 4.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_001098627 IRF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7808907 6.08E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001098627 IRF5 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs10488631 4.00E-11 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001098627 IRF5 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs10488631 2.00E-07 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_001098627 IRF5 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs10488631 3.00E-10 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_001098627 IRF5 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 1.65E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001098627 IRF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10488631 2.48E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001098627 IRF5 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 2.00E-11 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_001098627 IRF5 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs10488631 7.00E-18 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_001098627 IRF5 20383147 http://www.ncbi.nlm.nih.gov/pubmed/20383147 "Scleroderma, Systemic" rs10488631 2.00E-13 Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. NHGRI|-1
NM_001098627 IRF5 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs10488631 4.00E-07 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_001098627 IRF5 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs4728142 2.00E-08 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001098627 IRF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs4728142 7.30E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001098627 IRF5 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs4728142 8.00E-19 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_001098629 IRF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7808907 6.08E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001098629 IRF5 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs10488631 4.00E-11 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001098629 IRF5 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs10488631 2.00E-07 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_001098629 IRF5 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs10488631 3.00E-10 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_001098629 IRF5 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 1.65E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001098629 IRF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10488631 2.48E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001098629 IRF5 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 2.00E-11 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_001098629 IRF5 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs10488631 7.00E-18 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_001098629 IRF5 20383147 http://www.ncbi.nlm.nih.gov/pubmed/20383147 "Scleroderma, Systemic" rs10488631 2.00E-13 Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. NHGRI|-1
NM_001098629 IRF5 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs10488631 4.00E-07 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_001098629 IRF5 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs4728142 2.00E-08 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001098629 IRF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs4728142 7.30E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001098629 IRF5 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs4728142 8.00E-19 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_001098630 IRF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7808907 6.08E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001098630 IRF5 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs10488631 4.00E-11 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001098630 IRF5 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs10488631 2.00E-07 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_001098630 IRF5 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs10488631 3.00E-10 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_001098630 IRF5 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 1.65E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001098630 IRF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10488631 2.48E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001098630 IRF5 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 2.00E-11 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_001098630 IRF5 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs10488631 7.00E-18 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_001098630 IRF5 20383147 http://www.ncbi.nlm.nih.gov/pubmed/20383147 "Scleroderma, Systemic" rs10488631 2.00E-13 Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. NHGRI|-1
NM_001098630 IRF5 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs10488631 4.00E-07 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_001098630 IRF5 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs4728142 2.00E-08 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001098630 IRF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs4728142 7.30E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001098630 IRF5 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs4728142 8.00E-19 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_001098721 GNG4 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Menopause rs291353 6.00E-06 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_001098722 GNG4 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Menopause rs291353 6.00E-06 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_001098725 TCL1A 21172079 http://www.ncbi.nlm.nih.gov/pubmed/21172079 Aromatase Inhibitors rs11849538 7.00E-07 Genome-wide case-control study of musculoskeletal adverse events and functional genomics in women receiving aromatase inhibitors: going beyond associations. NHGRI|-1
NM_001098725 TCL1A 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs2369304 9.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001098725 TCL1A 20876420 http://www.ncbi.nlm.nih.gov/pubmed/20876420 Aromatase Inhibitors rs7158782 8.00E-07 Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors. NHGRI|-1
NM_001098787 BET1L 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs11602954 1.00E-14 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001098787 BET1L 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs2280543 4.00E-12 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_001098796 TOX2 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs6031252 6.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001098796 TOX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6073330 3.85E-05 NBL-GWAS version 2 dbGaP|2895
NM_001098796 TOX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11696193 6.20E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001098797 TOX2 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs6031252 6.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001098797 TOX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6073330 3.85E-05 NBL-GWAS version 2 dbGaP|2895
NM_001098797 TOX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11696193 6.20E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001098798 TOX2 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs6031252 6.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001098798 TOX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6073330 3.85E-05 NBL-GWAS version 2 dbGaP|2895
NM_001098798 TOX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11696193 6.20E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001098816 ODZ4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7931512 9.62E-06 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001098816 ODZ4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs880762 1.49E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001098816 ODZ4 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs530965 4.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_001098816 ODZ4 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs12290811 4.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001098816 ODZ4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs489257 5.34E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001098816 ODZ4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs472186 2.71E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001098816 ODZ4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11237826 1.68E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001098816 ODZ4 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs1357339 5.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_001098816 ODZ4 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Mass Index rs1458095 7.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001098816 ODZ4 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs678021 2.95E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001098816 ODZ4 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2851687 2.83E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001098816 ODZ4 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs480213 2.69E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001098835 MS4A15 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs7930940 2.00E-10 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001099218 RAD51AP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2042079 3.40E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001099271 POC5 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2112347 2.00E-13 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001099272 BTBD9 17637780 http://www.ncbi.nlm.nih.gov/pubmed/17637780 Restless Legs Syndrome rs9296249 4.00E-18 Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. NHGRI|-1
NM_001099272 BTBD9 17634447 http://www.ncbi.nlm.nih.gov/pubmed/17634447 Restless Legs Syndrome rs3923809 1.00E-17 A genetic risk factor for periodic limb movements in sleep. NHGRI|-1
NM_001099289 SH3RF3 20885792 http://www.ncbi.nlm.nih.gov/pubmed/20885792 Alzheimer Disease rs4676049 4.00E-08 Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. NHGRI|-1
NM_001099336 C12orf42 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs10745954 2.00E-11 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001099336 C12orf42 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs10778213 1.00E-10 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_001099403 PRDM8 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs16998073 1.00E-21 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_001099404 SCN5A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs11129795 5.00E-10 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001099404 SCN5A 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs11129795 5.00E-14 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001099404 SCN5A 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12053903 1.00E-14 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001099404 SCN5A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs12053903 1.00E-07 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001099404 SCN5A 19389651 http://www.ncbi.nlm.nih.gov/pubmed/19389651 Electrocardiography rs7638909 2.00E-06 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. NHGRI|-1
NM_001099404 SCN5A 21347284 http://www.ncbi.nlm.nih.gov/pubmed/21347284 Electrocardiography rs3922844 3.00E-23 Genome-wide association studies of the PR interval in African Americans. NHGRI|-1
NM_001099404 SCN5A 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs11708996 6.00E-26 Genome-wide association study of PR interval. NHGRI|-1
NM_001099404 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11708996 7.00E-06 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001099404 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11710077 1.00E-06 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001099404 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9851724 6.00E-16 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001099405 SCN5A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs11129795 5.00E-10 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001099405 SCN5A 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs11129795 5.00E-14 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001099405 SCN5A 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12053903 1.00E-14 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001099405 SCN5A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs12053903 1.00E-07 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001099405 SCN5A 19389651 http://www.ncbi.nlm.nih.gov/pubmed/19389651 Electrocardiography rs7638909 2.00E-06 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. NHGRI|-1
NM_001099405 SCN5A 21347284 http://www.ncbi.nlm.nih.gov/pubmed/21347284 Electrocardiography rs3922844 3.00E-23 Genome-wide association studies of the PR interval in African Americans. NHGRI|-1
NM_001099405 SCN5A 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs11708996 6.00E-26 Genome-wide association study of PR interval. NHGRI|-1
NM_001099405 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11708996 7.00E-06 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001099405 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11710077 1.00E-06 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001099405 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9851724 6.00E-16 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001099409 EHBP1L1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs6591182 9.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001099414 HAVCR1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs1501908 1.00E-11 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001099432 BCAS3 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs8068952 3.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_001099432 BCAS3 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Creatinine rs9895661 1.00E-15 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001099436 ULK3 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs6495122 2.00E-10 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001099436 ULK3 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs6495122 6.00E-07 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_001099645 RPL22L1 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs4955755 7.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_001099650 GXYLT1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2220999 1.09E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001099650 GXYLT1 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 "Cholesterol, HDL" rs871392 3.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001099650 GXYLT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11532502 1.30E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001099650 GXYLT1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10880174 5.06E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001099650 GXYLT1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10785303 5.06E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001099650 GXYLT1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs1472402 8.20E-06 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001099650 GXYLT1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs978797 3.38E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001099667 ARMS2 20861866 http://www.ncbi.nlm.nih.gov/pubmed/20861866 Macular Degeneration rs10490924 1.00E-60 Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. NHGRI|-1
NM_001099667 ARMS2 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs10490924 4E-322 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001099667 ARMS2 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs10490924 5.00E-119 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_001099667 ARMS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10490924 9.55E-15 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001099667 ARMS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2014307 1.48E-23 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001099667 ARMS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2014307 4.35E-08 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001099667 ARMS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2014307 4.49E-21 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001099667 ARMS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2014307 5.43E-07 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001099667 ARMS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2280141 1.06E-21 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001099667 ARMS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2280141 1.37E-23 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001099667 ARMS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2292627 2.68E-17 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001099667 ARMS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2292627 4.68E-18 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001099667 ARMS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1882907 4.02E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001099667 ARMS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1882907 6.27E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001099677 C8orf79 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Survival rs4831837 5.00E-07 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_001099691 TGFA 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs454305 5.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001099691 TGFA 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs432203 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001099772 CYP4B1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11583588 6.44E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001099784 FBXL19 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs10782001 9.00E-10 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_001099791 SYS1 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs1008953 1.00E-07 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_001099952 ITPR1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs746039 2.06E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001100120 ECE2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs3914188 3.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001100121 ECE2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs3914188 3.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001100163 MRVI1 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7940646 1.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001100163 MRVI1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2018368 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001100163 MRVI1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11042937 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001100164 PHACTR2 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs11155313 2.07E-05 Tier2a Allelic Association of Parkinson's Disease with Case-Unrelated Control Pairs dbGaP|2841
NM_001100165 PHACTR2 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs11155313 2.07E-05 Tier2a Allelic Association of Parkinson's Disease with Case-Unrelated Control Pairs dbGaP|2841
NM_001100166 PHACTR2 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs11155313 2.07E-05 Tier2a Allelic Association of Parkinson's Disease with Case-Unrelated Control Pairs dbGaP|2841
NM_001100167 MRVI1 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7940646 1.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001100167 MRVI1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2018368 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001100167 MRVI1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11042937 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001100168 CCR5 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs6441975 5.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_001100391 RALYL 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs7837606 1.08E-06 NBL-GWAS version 1 dbGaP|2845
NM_001100391 RALYL 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1427065 2.79E-07 NBL-GWAS version 1 dbGaP|2845
NM_001100391 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs6473383 2.29E-05 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_001100391 RALYL 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs6473383 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_001100391 RALYL 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs1375785 8.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001100391 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6473464 8.19E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001100391 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4524788 5.67E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001100391 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs7006609 6.24E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001100391 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6980733 1.02E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001100391 RALYL 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs731956 4.54E-06 NBL-GWAS version 1 dbGaP|2845
NM_001100392 RALYL 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs7837606 1.08E-06 NBL-GWAS version 1 dbGaP|2845
NM_001100392 RALYL 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1427065 2.79E-07 NBL-GWAS version 1 dbGaP|2845
NM_001100392 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs6473383 2.29E-05 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_001100392 RALYL 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs6473383 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_001100392 RALYL 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs1375785 8.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001100392 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6473464 8.19E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001100392 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4524788 5.67E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001100392 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs7006609 6.24E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001100392 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6980733 1.02E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001100392 RALYL 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs731956 4.54E-06 NBL-GWAS version 1 dbGaP|2845
NM_001100393 RALYL 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs7837606 1.08E-06 NBL-GWAS version 1 dbGaP|2845
NM_001100393 RALYL 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1427065 2.79E-07 NBL-GWAS version 1 dbGaP|2845
NM_001100393 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs6473383 2.29E-05 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_001100393 RALYL 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs6473383 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_001100393 RALYL 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs1375785 8.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001100393 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6473464 8.19E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001100393 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4524788 5.67E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001100393 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs7006609 6.24E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001100393 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6980733 1.02E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001100393 RALYL 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs731956 4.54E-06 NBL-GWAS version 1 dbGaP|2845
NM_001100397 RAPGEF4 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs6433379 1.00E-08 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001100397 RAPGEF4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs10187560 8.98E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001100398 RAP1GAP2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs12603284 3.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001100407 C17orf62 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Insulin-Like Growth Factor I rs9303029 4.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001100408 C17orf62 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Insulin-Like Growth Factor I rs9303029 4.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001100422 SPATS2L 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs1569175 9.00E-07 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001100422 SPATS2L 19727025 http://www.ncbi.nlm.nih.gov/pubmed/19727025 Exercise rs12612420 8.00E-06 Genome-wide association study of exercise behavior in Dutch and American adults. NHGRI|-1
NM_001100423 SPATS2L 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs1569175 9.00E-07 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001100423 SPATS2L 19727025 http://www.ncbi.nlm.nih.gov/pubmed/19727025 Exercise rs12612420 8.00E-06 Genome-wide association study of exercise behavior in Dutch and American adults. NHGRI|-1
NM_001100424 SPATS2L 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs1569175 9.00E-07 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001100424 SPATS2L 19727025 http://www.ncbi.nlm.nih.gov/pubmed/19727025 Exercise rs12612420 8.00E-06 Genome-wide association study of exercise behavior in Dutch and American adults. NHGRI|-1
NM_001100426 RAP1GDS1 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Triglycerides rs10516430 6.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001100427 RAP1GDS1 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Triglycerides rs10516430 6.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001100428 RAP1GDS1 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Triglycerides rs10516430 6.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001100429 RAP1GDS1 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Triglycerides rs10516430 6.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001100430 RAP1GDS1 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Triglycerides rs10516430 6.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001100590 KIAA0232 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4626203 7.83E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001100594 SNRK 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs17075286 8.00E-07 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_001100619 CABLES1 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs11082304 6.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001100619 CABLES1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs4800148 4.00E-09 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001100619 CABLES1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs4369779 3.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001100619 CABLES1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs4369779 6.86E-04 Genome-wide association between genotype and incident stroke in participants of primarily self-described European ancestry dbGaP|2886
NM_001100626 ERLIN1 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs11597390 2.00E-08 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_001100818 PID1 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs6436839 3.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001100875 10-Mar 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs2251393 4.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001101341 SFTA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4902467 7.98E-05 NBL-GWAS version 2 dbGaP|2895
NM_001101376 FAM183A 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs16830359 1.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001101417 ISPD 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10486776 6.16E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001101417 ISPD 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10486776 6.00E-06 A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. NHGRI|-1
NM_001101421 MYO1H 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs9943753 3.00E-06 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001101426 ISPD 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10486776 6.16E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001101426 ISPD 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10486776 6.00E-06 A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. NHGRI|-1
NM_001101654 CXXC1 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs1036935 2.00E-06 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_001101669 INPP4B 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs17007695 9.00E-07 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001101676 SAMD12 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs723268 8.86E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001101802 PHF21A 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs16938437 6.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001101802 PHF21A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11038830 1.81E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001102 ACTN1 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs2268983 7.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001102402 PCTP 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs1431318 9.00E-07 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_001102402 PCTP 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs8065311 2.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_001102406 ALPK1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs7658978 3.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001102416 KNG1 20303064 http://www.ncbi.nlm.nih.gov/pubmed/20303064 Partial Thromboplastin Time rs710446 1.00E-21 "Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time." NHGRI|-1
NM_001102416 KNG1 20876611 http://www.ncbi.nlm.nih.gov/pubmed/20876611 Adiponectin rs11924390 2.00E-09 Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ. NHGRI|-1
NM_001102420 ZFAND5 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs11143230 7.00E-06 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_001102420 ZFAND5 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs11143230 8.00E-07 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_001102421 ZFAND5 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs11143230 7.00E-06 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_001102421 ZFAND5 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs11143230 8.00E-07 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_001102426 TBC1D8 20548944 http://www.ncbi.nlm.nih.gov/pubmed/20548944 Osteoporosis rs2278729 1.00E-07 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. NHGRI|-1
NM_001102445 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2343331 2.46E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001102445 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2343278 9.28E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001102445 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2841974 4.67E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001102445 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2841979 9.97E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001102467 AQP12B 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs4676406 8.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001102469 LIPN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs303478 1.27E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001102469 LIPN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs303499 4.14E-06 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001102469 LIPN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs303502 1.54E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001102562 11-Mar 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs13158763 4.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001102562 11-Mar 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs163065 1.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001102562 11-Mar 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs171817 3.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001102564 C14orf179 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs935334 3.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001102575 SNX18 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4865879 6.81E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001102575 SNX18 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10940434 3.27E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001102614 POLR2A 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Sex Hormone-Binding Globulin rs6761 3.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001102654 NTF3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7302032 4.99E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001102669 RRAS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11023186 9.66E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001103184 FMN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6495001 8.90E-05 NBL-GWAS version 2 dbGaP|2895
NM_001103184 FMN1 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs1258763 1.00E-06 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_001104 ACTN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10791881 1.93E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001104 ACTN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10791881 6.16E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001104554 PAQR5 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11072089 3.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001104629 C4orf19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6830100 1.86E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001104631 PDE4D 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs10052657 2.00E-19 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001104631 PDE4D 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs1823068 3.00E-08 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_001104631 PDE4D 17667963 http://www.ncbi.nlm.nih.gov/pubmed/17667963 Neurotic Disorders rs702543 2.00E-06 A whole genome association study of neuroticism using DNA pooling. NHGRI|-1
NM_001104631 PDE4D 19426955 http://www.ncbi.nlm.nih.gov/pubmed/19426955 Asthma rs1588265 3.00E-08 Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. NHGRI|-1
NM_001105 ACVR1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10183640 5.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001105 ACVR1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2444769 9.19E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001105077 MECOM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs16852880 9.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001105078 MECOM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs16852880 9.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001105192 TLE3 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs6494849 7.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001105243 PCDH19 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs5921594 3.79E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001105244 PTPRM 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs7243299 8.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001105244 PTPRM 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs8098064 4.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001105244 PTPRM 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs12455846 5.15E-06 NBL-GWAS version 1 dbGaP|2845
NM_001105244 PTPRM 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs16951664 6.29E-06 NBL-GWAS version 1 dbGaP|2845
NM_001105250 NRXN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17107542 7.51E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001105250 NRXN3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs918270 5.55E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001105250 NRXN3 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10150332 3.00E-11 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001105250 NRXN3 19557197 http://www.ncbi.nlm.nih.gov/pubmed/19557197 Waist Circumference rs10146997 5.00E-08 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. NHGRI|-1
NM_001105250 NRXN3 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs11624704 3.00E-09 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001105515 ABCC4 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4148546 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001105515 ABCC4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1189428 2.40E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001105515 ABCC4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4148490 2.10E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001105515 ABCC4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4148475 4.40E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001105515 ABCC4 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs1926657 2.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001105515 ABCC4 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs9302001 3.00E-07 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_001105521 JAKMIP3 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs7098827 3.40E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001105528 C18orf34 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9956150 5.48E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001105529 ATP8A1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs13139219 7.85E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001105539 ZBTB10 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs272594 1.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001105539 ZBTB10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6992476 9.10E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001105540 DGKZ 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11038871 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_001105541 NEFM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1457266 4.27E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001105543 PLXNA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3734991 1.62E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001105543 PLXNA4 17903300 http://www.ncbi.nlm.nih.gov/pubmed/17903300 Body Mass Index rs1106683 1.00E-07 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. NHGRI|-1
NM_001105543 PLXNA4 17903300 http://www.ncbi.nlm.nih.gov/pubmed/17903300 Body Mass Index rs1106684 2.00E-06 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. NHGRI|-1
NM_001105563 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs1265086 2.69E-11 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001105563 CCHCR1 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 "Colitis, Ulcerative" rs9263739 4.00E-67 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_001105563 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11967883 3.15E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001105563 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs1265078 2.04E-21 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001105563 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs17196989 3.96E-10 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001105563 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9263749 5.60E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001105563 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111962041 4.16E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001105563 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113481038 8.56E-14 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001105563 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3130453 2.06E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001105563 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3094187 3.73E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001105564 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs1265086 2.69E-11 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001105564 CCHCR1 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 "Colitis, Ulcerative" rs9263739 4.00E-67 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_001105564 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11967883 3.15E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001105564 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs1265078 2.04E-21 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001105564 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs17196989 3.96E-10 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001105564 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9263749 5.60E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001105564 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111962041 4.16E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001105564 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113481038 8.56E-14 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001105564 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3130453 2.06E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001105564 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3094187 3.73E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001105580 GABRR3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7638369 4.19E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001105580 GABRR3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7638369 7.15E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001105581 LRRC30 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs12455846 5.15E-06 NBL-GWAS version 1 dbGaP|2845
NM_001105581 LRRC30 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs16951664 6.29E-06 NBL-GWAS version 1 dbGaP|2845
NM_001105659 LRRIQ3 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs11210359 8.00E-06 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_001109619 HIGD1C 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs12304921 7.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001109662 C12orf51 21270382 http://www.ncbi.nlm.nih.gov/pubmed/21270382 Alcohol Drinking rs2074356 9.00E-59 Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men. NHGRI|-1
NM_001109662 C12orf51 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs2074356 2.00E-31 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001109662 C12orf51 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Waist-Hip Ratio rs2074356 8.00E-12 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001109662 C12orf51 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs11066280 1.00E-35 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_001109662 C12orf51 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs11066280 8.00E-31 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_001109662 C12orf51 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs11066280 2.00E-15 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001109763 GSG1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs8051871 1.14E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001109809 ZFP57 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal Neoplasms rs3129055 7.00E-11 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_001109809 ZFP57 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3131863 5.63E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001109878 TBX22 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1474563 3.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001109879 TBX22 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1474563 3.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001110514 EBF4 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1810636 1.00E-10 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001111018 NAV2 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs874426 4.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_001111019 NAV2 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs874426 4.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_001111031 ACVR1C 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2444769 9.19E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001111032 ACVR1C 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2444769 9.19E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001111033 ACVR1C 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2444769 9.19E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001111034 ACP5 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs7253363 9.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001111035 ACP5 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs7253363 9.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001111036 ACP5 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs7253363 9.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001111067 ACVR1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10183640 5.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001111067 ACVR1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2444769 9.19E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001111077 EZR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs744893 2.53E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001111101 CNRIP1 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Sphingomyelins rs9309413 2.00E-09 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_001111283 IGF1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs5742692 4.00E-08 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001111283 IGF1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs35767 3.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001111283 IGF1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Insulin Resistance rs35767 2.00E-09 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001111283 IGF1 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs2172873 2.00E-06 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_001111283 IGF1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs1520223 9.00E-07 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001111284 IGF1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs5742692 4.00E-08 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001111284 IGF1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs35767 3.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001111284 IGF1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Insulin Resistance rs35767 2.00E-09 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001111284 IGF1 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs2172873 2.00E-06 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_001111284 IGF1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs1520223 9.00E-07 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001111285 IGF1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs5742692 4.00E-08 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001111285 IGF1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs35767 3.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001111285 IGF1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Insulin Resistance rs35767 2.00E-09 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001111285 IGF1 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs2172873 2.00E-06 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_001111285 IGF1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs1520223 9.00E-07 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001111298 PPIL6 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs9487094 4.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001112 ADARB1 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Respiratory Function Tests rs2838815 3.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_001112704 VAX1 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs7078160 2.00E-08 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_001112736 C3orf63 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs9835332 5.00E-13 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001112800 SLC8A1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs977867 4.31E-06 NBL-GWAS version 1 dbGaP|2845
NM_001112800 SLC8A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7569590 3.30E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001112800 SLC8A1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs719593 5.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001112801 SLC8A1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs977867 4.31E-06 NBL-GWAS version 1 dbGaP|2845
NM_001112801 SLC8A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7569590 3.30E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001112801 SLC8A1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs719593 5.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001112802 SLC8A1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs977867 4.31E-06 NBL-GWAS version 1 dbGaP|2845
NM_001112802 SLC8A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7569590 3.30E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001112802 SLC8A1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs719593 5.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001112808 TNNI3K 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs1514175 8.00E-14 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001112812 GRIA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10895889 7.40E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001113178 NFAT5 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1364063 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001113226 NTNG1 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs10494067 6.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_001113228 NTNG1 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs10494067 6.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_001113239 HIPK2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs10954654 2.79E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001113380 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2343331 2.46E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001113380 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2343278 9.28E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001113380 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2841974 4.67E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001113380 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2841979 9.97E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001113381 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2343331 2.46E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001113381 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2343278 9.28E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001113381 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2841974 4.67E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001113381 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2841979 9.97E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001113397 ZNF385B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1517702 3.83E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001113397 ZNF385B 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs16866933 6.00E-14 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001113397 ZNF385B 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4556941 8.69E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001113397 ZNF385B 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4556941 8.25E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001113398 ZNF385B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1517702 3.83E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001113398 ZNF385B 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs16866933 6.00E-14 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001113398 ZNF385B 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4556941 8.69E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001113398 ZNF385B 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4556941 8.25E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001113411 FGGY 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 "Diabetes Mellitus, Type 2" rs17119280 7.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_001113411 FGGY 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs12727131 3.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001113411 FGGY 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs4601609 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001113434 C17orf51 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs1975974 1.00E-07 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_001113434 C17orf51 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4889730 2.83E-11 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001113490 AMOT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs547425 1.12E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001113490 AMOT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs648170 7.30E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001113491 9-Sep 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs9906155 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001113491 9-Sep 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs647861 5.97E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001113492 9-Sep 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs9906155 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001113492 9-Sep 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs647861 5.97E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001113493 9-Sep 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs9906155 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001113493 9-Sep 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs647861 5.97E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001113494 9-Sep 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs9906155 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001113494 9-Sep 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs647861 5.97E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001113495 9-Sep 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs9906155 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001113495 9-Sep 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs647861 5.97E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001113496 9-Sep 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs9906155 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001113496 9-Sep 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs647861 5.97E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001113498 MDGA2 18762592 http://www.ncbi.nlm.nih.gov/pubmed/18762592 Neurotic Disorders rs12883384 7.00E-07 Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism. NHGRI|-1
NM_001113498 MDGA2 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Blood Viscosity rs7159841 2.00E-07 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001113511 ARHGEF7 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs4773330 8.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_001113512 ARHGEF7 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs4773330 8.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_001113513 ARHGEF7 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs4773330 8.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_001113523 PARP15 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs2650951 1.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001113755 TYMP 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs470119 4.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001113756 TYMP 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs470119 4.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001114086 CLIC5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4714860 7.86E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001114092 THUMPD3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2600178 1.52E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001114099 SEZ6L2 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Waist Circumference rs4787483 2.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001114100 SEZ6L2 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Waist Circumference rs4787483 2.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001114106 SLC44A3 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs12029080 6.00E-52 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001114132 NBEAL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10182274 9.90E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001114173 CTSC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17754282 4.30E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001114183 GRIA1 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Height rs12658202 9.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001114183 GRIA1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs12189362 3.00E-10 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001114185 MVK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs3759387 9.45E-05 NBL-GWAS version 2 dbGaP|2895
NM_001114309 ELF3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4436440 5.16E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001114309 ELF3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10800812 1.62E-08 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001114309 ELF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2819358 1.39E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001114380 ITGAL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2285459 3.38E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001114382 TSC2 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs2516739 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001114393 PAPD4 20673876 http://www.ncbi.nlm.nih.gov/pubmed/20673876 "Depressive Disorder, Major" rs7713917 1.00E-06 "Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression." NHGRI|-1
NM_001114393 PAPD4 21700879 http://www.ncbi.nlm.nih.gov/pubmed/21700879 Adiponectin rs13358260 5.00E-06 Novel Locus FER Is Associated With Serum HMW Adiponectin Levels. NHGRI|-1
NM_001114394 PAPD4 20673876 http://www.ncbi.nlm.nih.gov/pubmed/20673876 "Depressive Disorder, Major" rs7713917 1.00E-06 "Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression." NHGRI|-1
NM_001114394 PAPD4 21700879 http://www.ncbi.nlm.nih.gov/pubmed/21700879 Adiponectin rs13358260 5.00E-06 Novel Locus FER Is Associated With Serum HMW Adiponectin Levels. NHGRI|-1
NM_001114617 MGAT1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 "Cholesterol, HDL" rs655601 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001114617 MGAT1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs12517906 6.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001114617 MGAT1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs12517906 7.00E-08 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001114618 MGAT1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 "Cholesterol, HDL" rs655601 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001114618 MGAT1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs12517906 6.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001114618 MGAT1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs12517906 7.00E-08 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001114619 MGAT1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 "Cholesterol, HDL" rs655601 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001114619 MGAT1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs12517906 6.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001114619 MGAT1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs12517906 7.00E-08 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001114620 MGAT1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 "Cholesterol, HDL" rs655601 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001114620 MGAT1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs12517906 6.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001114620 MGAT1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs12517906 7.00E-08 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001114634 PLAG1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10958476 7.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001114634 PLAG1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs7833986 8.00E-10 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001114634 PLAG1 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Body Height rs13273123 1.00E-09 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001114634 PLAG1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs13273123 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001114635 PLAG1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10958476 7.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001114635 PLAG1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs7833986 8.00E-10 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001114635 PLAG1 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Body Height rs13273123 1.00E-09 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001114635 PLAG1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs13273123 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001114636 FANCL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs848291 3.41E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001114753 ENG 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Blood Pressure rs7865146 1.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001114937 SH2D1A 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1846322 9.49E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001114937 SH2D1A 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1781115 1.67E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001114978 TP63 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs4488809 7.00E-26 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_001114978 TP63 20871597 http://www.ncbi.nlm.nih.gov/pubmed/20871597 Lung Neoplasms rs10937405 7.00E-12 Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations. NHGRI|-1
NM_001114978 TP63 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1515496 8.68E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001114978 TP63 18794855 http://www.ncbi.nlm.nih.gov/pubmed/18794855 Urinary Bladder Neoplasms rs710521 1.00E-07 Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001114978 TP63 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs710521 2.00E-10 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_001114978 TP63 20348956 http://www.ncbi.nlm.nih.gov/pubmed/20348956 Urinary Bladder Neoplasms rs710521 6.00E-08 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001114979 TP63 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs4488809 7.00E-26 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_001114979 TP63 20871597 http://www.ncbi.nlm.nih.gov/pubmed/20871597 Lung Neoplasms rs10937405 7.00E-12 Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations. NHGRI|-1
NM_001114979 TP63 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1515496 8.68E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001114979 TP63 18794855 http://www.ncbi.nlm.nih.gov/pubmed/18794855 Urinary Bladder Neoplasms rs710521 1.00E-07 Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001114979 TP63 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs710521 2.00E-10 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_001114979 TP63 20348956 http://www.ncbi.nlm.nih.gov/pubmed/20348956 Urinary Bladder Neoplasms rs710521 6.00E-08 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001114980 TP63 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs4488809 7.00E-26 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_001114980 TP63 20871597 http://www.ncbi.nlm.nih.gov/pubmed/20871597 Lung Neoplasms rs10937405 7.00E-12 Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations. NHGRI|-1
NM_001114980 TP63 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1515496 8.68E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001114980 TP63 18794855 http://www.ncbi.nlm.nih.gov/pubmed/18794855 Urinary Bladder Neoplasms rs710521 1.00E-07 Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001114980 TP63 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs710521 2.00E-10 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_001114980 TP63 20348956 http://www.ncbi.nlm.nih.gov/pubmed/20348956 Urinary Bladder Neoplasms rs710521 6.00E-08 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001114981 TP63 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs4488809 7.00E-26 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_001114981 TP63 20871597 http://www.ncbi.nlm.nih.gov/pubmed/20871597 Lung Neoplasms rs10937405 7.00E-12 Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations. NHGRI|-1
NM_001114981 TP63 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1515496 8.68E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001114981 TP63 18794855 http://www.ncbi.nlm.nih.gov/pubmed/18794855 Urinary Bladder Neoplasms rs710521 1.00E-07 Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001114981 TP63 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs710521 2.00E-10 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_001114981 TP63 20348956 http://www.ncbi.nlm.nih.gov/pubmed/20348956 Urinary Bladder Neoplasms rs710521 6.00E-08 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001114982 TP63 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs4488809 7.00E-26 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_001114982 TP63 20871597 http://www.ncbi.nlm.nih.gov/pubmed/20871597 Lung Neoplasms rs10937405 7.00E-12 Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations. NHGRI|-1
NM_001114982 TP63 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1515496 8.68E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001114982 TP63 18794855 http://www.ncbi.nlm.nih.gov/pubmed/18794855 Urinary Bladder Neoplasms rs710521 1.00E-07 Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001114982 TP63 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs710521 2.00E-10 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_001114982 TP63 20348956 http://www.ncbi.nlm.nih.gov/pubmed/20348956 Urinary Bladder Neoplasms rs710521 6.00E-08 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001115 ADCY8 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs263238 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001115016 KIAA1310 21046636 http://www.ncbi.nlm.nih.gov/pubmed/21046636 Brain Waves rs4907240 4.00E-06 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. NHGRI|-1
NM_001115156 GDI2 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2380205 5.00E-07 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001116 ADCY9 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2444217 9.00E-08 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001116 ADCY9 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs2601828 1.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_001118 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2267727 3.79E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001118 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2267742 4.79E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001118 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1558477 2.58E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001118 ADCYAP1R1 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1558477 3.00E-07 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001118 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7791986 8.41E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001118885 GLRA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs3020867 1.46E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001118886 GLRA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs3020867 1.46E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001121 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7090030 7.39E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001121 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11194995 7.62E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001121 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11194996 7.62E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001121 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11195001 7.19E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001121 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7917994 8.56E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001121 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7921757 8.56E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001121 ADD3 20460270 http://www.ncbi.nlm.nih.gov/pubmed/20460270 Biliary Atresia rs17095355 7.00E-09 Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. NHGRI|-1
NM_001122607 RUNX1 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs2014300 8.00E-22 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001122608 HCCS 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs5934953 1.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001122630 CDKN1C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2078786 9.55E-06 NBL-GWAS version 2 dbGaP|2895
NM_001122631 CDKN1C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2078786 9.55E-06 NBL-GWAS version 2 dbGaP|2895
NM_001122633 CPS1 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Creatinine rs1047891 1.00E-15 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001122633 CPS1 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs1047891 9.00E-09 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_001122633 CPS1 20154341 http://www.ncbi.nlm.nih.gov/pubmed/20154341 Homocysteine rs1047891 5.00E-09 Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults. NHGRI|-1
NM_001122634 CPS1 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Creatinine rs1047891 1.00E-15 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001122634 CPS1 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs1047891 9.00E-09 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_001122634 CPS1 20154341 http://www.ncbi.nlm.nih.gov/pubmed/20154341 Homocysteine rs1047891 5.00E-09 Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults. NHGRI|-1
NM_001122659 EDNRB 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs9574199 7.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001122659 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6563036 6.86E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001122659 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7996252 2.72E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001122659 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7996252 8.44E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001122659 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2248525 3.14E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001122659 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2248525 8.12E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001122659 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2265775 5.77E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001122659 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2987526 3.23E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001122679 ODZ2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17384913 1.26E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001122679 ODZ2 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs2122554 3.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001122679 ODZ2 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs17404956 1.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001122740 ESR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2941740 2.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001122740 ESR1 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs1999805 2.00E-08 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_001122740 ESR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2504063 6.00E-11 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001122740 ESR1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs543650 1.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001122740 ESR1 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs6902771 8.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_001122740 ESR1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs2982694 7.00E-10 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001122740 ESR1 19219042 http://www.ncbi.nlm.nih.gov/pubmed/19219042 Breast Neoplasms rs2046210 2.00E-15 Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. NHGRI|-1
NM_001122741 ESR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2941740 2.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001122741 ESR1 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs1999805 2.00E-08 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_001122741 ESR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2504063 6.00E-11 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001122741 ESR1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs543650 1.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001122741 ESR1 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs6902771 8.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_001122741 ESR1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs2982694 7.00E-10 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001122741 ESR1 19219042 http://www.ncbi.nlm.nih.gov/pubmed/19219042 Breast Neoplasms rs2046210 2.00E-15 Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. NHGRI|-1
NM_001122742 ESR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2941740 2.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001122742 ESR1 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs1999805 2.00E-08 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_001122742 ESR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2504063 6.00E-11 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001122742 ESR1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs543650 1.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001122742 ESR1 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs6902771 8.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_001122742 ESR1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs2982694 7.00E-10 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001122742 ESR1 19219042 http://www.ncbi.nlm.nih.gov/pubmed/19219042 Breast Neoplasms rs2046210 2.00E-15 Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. NHGRI|-1
NM_001122769 LCA5 21190210 http://www.ncbi.nlm.nih.gov/pubmed/21190210 Obsessive-Compulsive Disorder rs3747767 7.00E-07 Genome-wide association study of hoarding traits. NHGRI|-1
NM_001122821 SET 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4836618 5.41E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001122824 TACC1 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs7832232 5.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_001122838 NAPEPLD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1968199 1.46E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001122951 DARC 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs2814778 1.00E-08 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001122951 DARC 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Chemokine CCL2 rs10489849 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001122964 SMEK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Blood Pressure rs10496050 1.28E-05 Genomewide association analysis of systolic blood pressure (SBP) in a birth cohort from a founder population dbGaP|2903
NM_001123041 CCR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9990343 2.76E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001123041 CCR2 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs9990343 4.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001123041 CCR2 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs6441961 3.00E-07 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_001123065 C7orf65 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs12670472 2.77E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001123066 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17563986 3.44E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001123066 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs242557 9.00E-18 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_001123066 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1981997 2.02E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001123066 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs8070723 3.36E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001123066 MAPT 21044948 http://www.ncbi.nlm.nih.gov/pubmed/21044948 Parkinson Disease rs8070723 7.00E-12 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. NHGRI|-1
NM_001123066 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs8070723 2.00E-118 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_001123067 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17563986 3.44E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001123067 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs242557 9.00E-18 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_001123067 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1981997 2.02E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001123067 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs8070723 3.36E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001123067 MAPT 21044948 http://www.ncbi.nlm.nih.gov/pubmed/21044948 Parkinson Disease rs8070723 7.00E-12 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. NHGRI|-1
NM_001123067 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs8070723 2.00E-118 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_001123376 TMEM72 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11239177 3.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001123376 TMEM72 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1480597 1.33E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001123376 TMEM72 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1480597 2.00E-06 Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_001123376 TMEM72 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1480597 3.08E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001123376 TMEM72 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4356177 5.00E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001123376 TMEM72 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs999473 7.83E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001123376 TMEM72 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7097094 7.83E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001123376 TMEM72 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs7911712 6.00E-06 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_001123377 PARK7 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs35675666 5.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001123377 PARK7 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs12727642 9.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001123396 CCR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9990343 2.76E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001123396 CCR2 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs9990343 4.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001123396 CCR2 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs6441961 3.00E-07 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_001124 ADM 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Bipolar Disorder rs6484218 4.00E-08 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_001126044 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001126044 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 8.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001126044 PTGER3 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs10458561 4.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NM_001126060 NOS1AP 20062061 http://www.ncbi.nlm.nih.gov/pubmed/20062061 Electrocardiography rs1415259 7.00E-10 Genetic variation in SCN10A influences cardiac conduction. NHGRI|-1
NM_001126060 NOS1AP 16648850 http://www.ncbi.nlm.nih.gov/pubmed/16648850 Electrocardiography rs10494366 1.00E-10 A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. NHGRI|-1
NM_001126060 NOS1AP 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs10494366 5.00E-22 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001126060 NOS1AP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12140791 5.12E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001126060 NOS1AP 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs16857031 1.00E-34 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001126060 NOS1AP 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12029454 3.00E-45 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001126060 NOS1AP 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs4657178 7.00E-33 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001126060 NOS1AP 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs2880058 2.00E-10 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001126060 NOS1AP 19587794 http://www.ncbi.nlm.nih.gov/pubmed/19587794 "Arrhythmias, Cardiac" rs12143842 1.00E-83 Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies. NHGRI|-1
NM_001126060 NOS1AP 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12143842 2.00E-78 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001126060 NOS1AP 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs12143842 2.00E-78 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001126111 OSGIN2 20018961 http://www.ncbi.nlm.nih.gov/pubmed/20018961 Leprosy rs40457 1.00E-12 Genomewide association study of leprosy. NHGRI|-1
NM_001126121 SLC25A19 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs9892996 2.23E-07 NBL-GWAS version 1 dbGaP|2845
NM_001126122 SLC25A19 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs9892996 2.23E-07 NBL-GWAS version 1 dbGaP|2845
NM_001126131 POLG 18193045 http://www.ncbi.nlm.nih.gov/pubmed/18193045 Body Height rs4932217 8.00E-07 Common variants in the GDF5-UQCC region are associated with variation in human height. NHGRI|-1
NM_001126181 NRGN 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs12807809 2.00E-09 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_001126328 LNX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1391759 1.78E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001126328 LNX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1391759 6.11E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001126328 LNX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1391758 1.84E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001126328 LNX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1391758 6.29E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001126335 SLC7A9 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Cystatin C rs12460876 3.00E-15 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001126335 SLC7A9 21572414 http://www.ncbi.nlm.nih.gov/pubmed/21572414 Metabolism rs8101881 6.00E-27 A genome-wide association study of metabolic traits in human urine. NHGRI|-1
NM_001126336 VCAN 20516156 http://www.ncbi.nlm.nih.gov/pubmed/20516156 "Depressive Disorder, Major" rs310501 7.00E-06 Genome-wide association study of major recurrent depression in the U.K. population. NHGRI|-1
NM_001127173 CADM3 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Chemokine CCL2 rs1474747 3.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001127183 CFLAR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12621441 3.43E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001127184 CFLAR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12621441 3.43E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001127190 CSK 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs1378942 1.00E-23 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_001127208 TET2 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs10005603 7.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_001127208 TET2 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs7679673 3.00E-14 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001127211 KIAA1598 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs7078160 2.00E-08 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_001127214 ACSF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3743979 2.02E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001127231 AUTS2 21471458 http://www.ncbi.nlm.nih.gov/pubmed/21471458 Alcohol Drinking rs6943555 4.00E-08 Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. NHGRI|-1
NM_001127231 AUTS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Body Mass Index rs10263639 3.04E-05 Genomewide association analysis of body mass index (BMI) in a birth cohort from a founder population dbGaP|2896
NM_001127231 AUTS2 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs10263639 3.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001127231 AUTS2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs6961611 7.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001127232 AUTS2 21471458 http://www.ncbi.nlm.nih.gov/pubmed/21471458 Alcohol Drinking rs6943555 4.00E-08 Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. NHGRI|-1
NM_001127232 AUTS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Body Mass Index rs10263639 3.04E-05 Genomewide association analysis of body mass index (BMI) in a birth cohort from a founder population dbGaP|2896
NM_001127232 AUTS2 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs10263639 3.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001127232 AUTS2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs6961611 7.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001127257 SLC39A10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1561451 8.86E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001127257 SLC39A10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6714748 1.98E-05 NBL-GWAS version 2 dbGaP|2895
NM_001127257 SLC39A10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4505549 4.83E-06 NBL-GWAS version 2 dbGaP|2895
NM_001127258 HHIPL1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs2895811 1.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001127323 GRM8 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Carotid Artery Diseases rs17691394 9.00E-07 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_001127323 GRM8 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs11971186 9.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NM_001127323 GRM8 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs17864092 6.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_001127328 ACADM 20037589 http://www.ncbi.nlm.nih.gov/pubmed/20037589 Nonalcoholic Fatty Liver Disease rs211718 1.00E-63 A genome-wide perspective of genetic variation in human metabolism. NHGRI|-1
NM_001127366 PAX3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs348970 1.96E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001127370 CDCA7L 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs1175000 5.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001127370 CDCA7L 17903292 http://www.ncbi.nlm.nih.gov/pubmed/17903292 Thyrotropin rs10499559 8.00E-06 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001127370 CDCA7L 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs13227860 1.26E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001127371 CDCA7L 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs1175000 5.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001127371 CDCA7L 17903292 http://www.ncbi.nlm.nih.gov/pubmed/17903292 Thyrotropin rs10499559 8.00E-06 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001127371 CDCA7L 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs13227860 1.26E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001127380 SAA2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs12282742 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001127381 PPP2R2B 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs1864982 3.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_001127381 PPP2R2B 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs9325032 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_001127384 CTNNA3 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs16922827 1.00E-09 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001127384 CTNNA3 19187332 http://www.ncbi.nlm.nih.gov/pubmed/19187332 Asthma rs10762058 6.00E-06 Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis. NHGRI|-1
NM_001127384 CTNNA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1948946 2.98E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001127384 CTNNA3 17158188 http://www.ncbi.nlm.nih.gov/pubmed/17158188 Tobacco Use Disorder rs4142041 6.00E-06 Novel genes identified in a high-density genome wide association study for nicotine dependence. NHGRI|-1
NM_001127384 CTNNA3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4746675 2.46E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001127385 CTXN3 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs245201 9.00E-08 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_001127385 CTXN3 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs374499 8.86E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001127394 TSEN15 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs2274432 8.00E-09 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001127399 YPEL5 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs7579944 1.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_001127400 YPEL5 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs7579944 1.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_001127401 YPEL5 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs7579944 1.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_001127441 CPA5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4731688 1.52E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001127442 CPA5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4731688 1.52E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001127443 CD36 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs10499859 3.00E-06 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NM_001127444 CD36 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs10499859 3.00E-06 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NM_001127457 CRY2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs11605924 1.00E-14 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001127461 NLRP3 20031576 http://www.ncbi.nlm.nih.gov/pubmed/20031576 Fibrinogen rs1539019 1.00E-08 Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. NHGRI|-1
NM_001127461 NLRP3 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs12239046 1.00E-15 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001127461 NLRP3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10399826 2.06E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001127461 NLRP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11802371 1.11E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001127462 NLRP3 20031576 http://www.ncbi.nlm.nih.gov/pubmed/20031576 Fibrinogen rs1539019 1.00E-08 Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. NHGRI|-1
NM_001127462 NLRP3 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs12239046 1.00E-15 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001127462 NLRP3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10399826 2.06E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001127462 NLRP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11802371 1.11E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001127464 ZNF469 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs12447690 6.00E-22 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_001127464 ZNF469 20485516 http://www.ncbi.nlm.nih.gov/pubmed/20485516 Cornea rs12447690 9.00E-11 Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. NHGRI|-1
NM_001127493 ANK2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4834308 6.98E-06 NBL-GWAS version 1 dbGaP|2845
NM_001127496 SPRY4 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs17577085 4.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001127496 SPRY4 20543847 http://www.ncbi.nlm.nih.gov/pubmed/20543847 Testicular Neoplasms rs4624820 1.00E-14 "Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer." NHGRI|-1
NM_001127496 SPRY4 19483681 http://www.ncbi.nlm.nih.gov/pubmed/19483681 Testicular Neoplasms rs4624820 3.00E-13 A genome-wide association study of testicular germ cell tumor. NHGRI|-1
NM_001127500 MET 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs10243024 6.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001127501 ALPL 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs1780324 7.00E-15 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_001127501 ALPL 20558539 http://www.ncbi.nlm.nih.gov/pubmed/20558539 Phosphorus rs1697421 1.00E-27 Common genetic variants associate with serum phosphorus concentration. NHGRI|-1
NM_001127507 BANK1 18204447 http://www.ncbi.nlm.nih.gov/pubmed/18204447 "Lupus Erythematosus, Systemic" rs10516487 4.00E-10 Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus. NHGRI|-1
NM_001127507 BANK1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7694392 4.26E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001127507 BANK1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4640677 6.62E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001127507 BANK1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs12648641 9.89E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001127598 IGF2 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs3741208 2.00E-07 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_001127598 IGF2 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 "Diabetes Mellitus, Type 1" rs1004446 4.00E-09 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NM_001127605 LIPA 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs1412444 3.00E-13 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_001127605 LIPA 21606135 http://www.ncbi.nlm.nih.gov/pubmed/21606135 Coronary Artery Disease rs1412444 4.00E-08 A Genome-wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease. NHGRI|-1
NM_001127615 ENOX1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs1324015 9.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001127649 PEX26 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs462904 3.01E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001127656 CSRP3 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs12146588 8.75E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001127668 KCNE1 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs727957 2.00E-12 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001127669 KCNE1 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs727957 2.00E-12 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001127670 KCNE1 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs727957 2.00E-12 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001127692 PCCA 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs681561 9.81E-07 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001127713 ATL1 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs17122693 3.00E-07 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001127715 STXBP5 20231535 http://www.ncbi.nlm.nih.gov/pubmed/20231535 Blood Coagulation Factors rs9390459 1.00E-22 "Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium." NHGRI|-1
NM_001127715 STXBP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs9390459 2.10E-04 Genome-wide association between genotype and incident heart failure in African-American participants dbGaP|2885
NM_001127715 STXBP5 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs9373523 1.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_001127892 SALL1 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs10521222 9.00E-13 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001127895 CHST8 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs4805924 6.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001127896 CHST8 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs4805924 6.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001127898 CLCN5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1553510 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001127899 CLCN5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1553510 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001128128 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2839658 1.84E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001128128 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2839658 8.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001128128 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12217563 3.40E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001128128 ZEB1 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001128141 DPEP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs154659 7.56E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001128141 DPEP1 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs154659 7.00E-08 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_001128142 RWDD3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1858111 4.19E-06 NBL-GWAS version 1 dbGaP|2845
NM_001128142 RWDD3 19207018 http://www.ncbi.nlm.nih.gov/pubmed/19207018 Pain Measurement rs6693882 2.00E-06 Genome-wide association study of acute post-surgical pain in humans. NHGRI|-1
NM_001128142 RWDD3 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1414896 2.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001128148 TFRC 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9859260 8.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001128148 TFRC 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs11915082 8.00E-13 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001128160 UBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1807844 5.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001128160 UBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1357540 2.69E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001128161 UBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1807844 5.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001128161 UBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1357540 2.69E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001128164 ATXN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs3812205 2.44E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001128164 ATXN1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs697739 4.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001128164 ATXN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1573134 5.35E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001128176 THRB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs9310736 3.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001128176 THRB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs9310736 4.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001128176 THRB 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs3903470 8.59E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001128177 THRB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs9310736 3.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001128177 THRB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs9310736 4.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001128177 THRB 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs3903470 8.59E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001128202 C10orf122 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs9422897 7.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001128209 SGCD 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Anthropometry rs157350 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001128209 SGCD 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Waist-Hip Ratio rs157350 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_001128209 SGCD 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs4704970 7.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001128210 SPRED2 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs934734 5.00E-10 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001128210 SPRED2 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs1876518 2.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_001128215 LIPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs303478 1.27E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001128215 LIPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs303499 4.14E-06 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001128215 LIPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs303502 1.54E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001128219 VGLL4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs892932 6.66E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001128219 VGLL4 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs6782029 9.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_001128220 VGLL4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs892932 6.66E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001128220 VGLL4 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs6782029 9.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_001128221 VGLL4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs892932 6.66E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001128221 VGLL4 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs6782029 9.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_001128303 C13orf31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3764147 7.36E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001128303 C13orf31 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs3764147 2.00E-13 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001128303 C13orf31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs3764147 1.21E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001128303 C13orf31 20018961 http://www.ncbi.nlm.nih.gov/pubmed/20018961 Leprosy rs3764147 4.00E-54 Genomewide association study of leprosy. NHGRI|-1
NM_001128303 C13orf31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2121037 4.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001128303 C13orf31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs10507522 1.33E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001128303 C13orf31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs687582 6.19E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001128427 FSTL5 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs17638464 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001128427 FSTL5 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs6840361 4.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001128427 FSTL5 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs4470583 4.00E-07 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_001128428 FSTL5 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs17638464 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001128428 FSTL5 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs6840361 4.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001128428 FSTL5 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs4470583 4.00E-07 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_001128429 SMARCAD1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11097407 4.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001128429 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11097407 2.46E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001128429 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2664871 2.59E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001128429 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2632401 1.74E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001128429 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2087170 3.46E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001128429 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12646184 1.96E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001128430 SMARCAD1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11097407 4.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001128430 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11097407 2.46E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001128430 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2664871 2.59E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001128430 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2632401 1.74E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001128430 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2087170 3.46E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001128430 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12646184 1.96E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001128595 TC2N 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17127600 2.74E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001128596 TC2N 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17127600 2.74E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001128602 RASGRP1 18840781 http://www.ncbi.nlm.nih.gov/pubmed/18840781 "Diabetes Mellitus, Type 1" rs8035957 4.00E-06 Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes. NHGRI|-1
NM_001128602 RASGRP1 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs12912251 1.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001128615 ARHGEF3 19110211 http://www.ncbi.nlm.nih.gov/pubmed/19110211 Platelet Count rs12485738 4.00E-27 A genome-wide association study identifies three loci associated with mean platelet volume. NHGRI|-1
NM_001128615 ARHGEF3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs12485738 6.00E-31 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001128615 ARHGEF3 21452313 http://www.ncbi.nlm.nih.gov/pubmed/21452313 "Arthritis, Rheumatoid" rs2062583 2.00E-06 Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci. NHGRI|-1
NM_001128616 ARHGEF3 19110211 http://www.ncbi.nlm.nih.gov/pubmed/19110211 Platelet Count rs12485738 4.00E-27 A genome-wide association study identifies three loci associated with mean platelet volume. NHGRI|-1
NM_001128616 ARHGEF3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs12485738 6.00E-31 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001128616 ARHGEF3 21452313 http://www.ncbi.nlm.nih.gov/pubmed/21452313 "Arthritis, Rheumatoid" rs2062583 2.00E-06 Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci. NHGRI|-1
NM_001128620 PAK1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1377470 9.03E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001128633 RIMBP3C 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs131654 1.00E-16 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_001128844 SMARCA4 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11669133 1.00E-08 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001128844 SMARCA4 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs1122608 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001128844 SMARCA4 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs1122608 2.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_001128844 SMARCA4 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs11668477 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001128844 SMARCA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs11668477 1.51E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001128845 SMARCA4 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11669133 1.00E-08 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001128845 SMARCA4 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs1122608 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001128845 SMARCA4 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs1122608 2.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_001128845 SMARCA4 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs11668477 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001128845 SMARCA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs11668477 1.51E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001128846 SMARCA4 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11669133 1.00E-08 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001128846 SMARCA4 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs1122608 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001128846 SMARCA4 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs1122608 2.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_001128846 SMARCA4 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs11668477 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001128846 SMARCA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs11668477 1.51E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001128847 SMARCA4 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11669133 1.00E-08 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001128847 SMARCA4 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs1122608 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001128847 SMARCA4 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs1122608 2.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_001128847 SMARCA4 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs11668477 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001128847 SMARCA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs11668477 1.51E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001128848 SMARCA4 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11669133 1.00E-08 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001128848 SMARCA4 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs1122608 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001128848 SMARCA4 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs1122608 2.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_001128848 SMARCA4 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs11668477 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001128848 SMARCA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs11668477 1.51E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001128849 SMARCA4 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11669133 1.00E-08 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001128849 SMARCA4 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs1122608 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001128849 SMARCA4 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs1122608 2.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_001128849 SMARCA4 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs11668477 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001128849 SMARCA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs11668477 1.51E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001128852 SRRT 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs12666989 2.00E-08 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_001128853 SRRT 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs12666989 2.00E-08 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_001128854 SRRT 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs12666989 2.00E-08 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_001128916 TOMM40 19125160 http://www.ncbi.nlm.nih.gov/pubmed/19125160 Alzheimer Disease rs157580 1.00E-40 Examination of the current top candidate genes for AD in a genome-wide association study. NHGRI|-1
NM_001128916 TOMM40 21123754 http://www.ncbi.nlm.nih.gov/pubmed/21123754 Alzheimer Disease rs157580 1.00E-06 "Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort." NHGRI|-1
NM_001128916 TOMM40 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs157580 8.00E-89 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_001128916 TOMM40 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, HDL" rs157580 4.00E-07 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001128916 TOMM40 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs157580 2.00E-19 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001128916 TOMM40 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs157580 5.00E-08 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001128916 TOMM40 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs157580 4.96E-08 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001128916 TOMM40 20460622 http://www.ncbi.nlm.nih.gov/pubmed/20460622 Alzheimer Disease rs2075650 1.00E-295 Genome-wide analysis of genetic loci associated with Alzheimer disease. NHGRI|-1
NM_001128916 TOMM40 21123754 http://www.ncbi.nlm.nih.gov/pubmed/21123754 Alzheimer Disease rs2075650 1.00E-06 "Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort." NHGRI|-1
NM_001128916 TOMM40 19734902 http://www.ncbi.nlm.nih.gov/pubmed/19734902 Alzheimer Disease rs2075650 2.00E-157 Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. NHGRI|-1
NM_001128916 TOMM40 19734903 http://www.ncbi.nlm.nih.gov/pubmed/19734903 Alzheimer Disease rs2075650 2.00E-16 Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. NHGRI|-1
NM_001128916 TOMM40 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs2075650 3.00E-11 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_001128916 TOMM40 20885792 http://www.ncbi.nlm.nih.gov/pubmed/20885792 Alzheimer Disease rs2075650 5.00E-36 Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. NHGRI|-1
NM_001128916 TOMM40 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs2075650 3.00E-19 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001128916 TOMM40 18439552 http://www.ncbi.nlm.nih.gov/pubmed/18439552 C-Reactive Protein rs2075650 1.00E-07 Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein. NHGRI|-1
NM_001128916 TOMM40 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs2075650 1.05E-05 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001128916 TOMM40 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs2075650 8.00E-12 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001128916 TOMM40 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs2075650 1.81E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001128917 TOMM40 19125160 http://www.ncbi.nlm.nih.gov/pubmed/19125160 Alzheimer Disease rs157580 1.00E-40 Examination of the current top candidate genes for AD in a genome-wide association study. NHGRI|-1
NM_001128917 TOMM40 21123754 http://www.ncbi.nlm.nih.gov/pubmed/21123754 Alzheimer Disease rs157580 1.00E-06 "Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort." NHGRI|-1
NM_001128917 TOMM40 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs157580 8.00E-89 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_001128917 TOMM40 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, HDL" rs157580 4.00E-07 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001128917 TOMM40 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs157580 2.00E-19 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001128917 TOMM40 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs157580 5.00E-08 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001128917 TOMM40 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs157580 4.96E-08 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001128917 TOMM40 20460622 http://www.ncbi.nlm.nih.gov/pubmed/20460622 Alzheimer Disease rs2075650 1.00E-295 Genome-wide analysis of genetic loci associated with Alzheimer disease. NHGRI|-1
NM_001128917 TOMM40 21123754 http://www.ncbi.nlm.nih.gov/pubmed/21123754 Alzheimer Disease rs2075650 1.00E-06 "Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort." NHGRI|-1
NM_001128917 TOMM40 19734902 http://www.ncbi.nlm.nih.gov/pubmed/19734902 Alzheimer Disease rs2075650 2.00E-157 Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. NHGRI|-1
NM_001128917 TOMM40 19734903 http://www.ncbi.nlm.nih.gov/pubmed/19734903 Alzheimer Disease rs2075650 2.00E-16 Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. NHGRI|-1
NM_001128917 TOMM40 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs2075650 3.00E-11 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_001128917 TOMM40 20885792 http://www.ncbi.nlm.nih.gov/pubmed/20885792 Alzheimer Disease rs2075650 5.00E-36 Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. NHGRI|-1
NM_001128917 TOMM40 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs2075650 3.00E-19 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001128917 TOMM40 18439552 http://www.ncbi.nlm.nih.gov/pubmed/18439552 C-Reactive Protein rs2075650 1.00E-07 Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein. NHGRI|-1
NM_001128917 TOMM40 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs2075650 1.05E-05 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001128917 TOMM40 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs2075650 8.00E-12 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001128917 TOMM40 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs2075650 1.81E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001128922 LRRC32 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3740778 7.68E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001128922 LRRC32 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2155219 5.00E-16 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001128922 LRRC32 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs7927894 1.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001128922 LRRC32 19349984 http://www.ncbi.nlm.nih.gov/pubmed/19349984 "Dermatitis, Atopic" rs7927894 8.00E-10 A common variant on chromosome 11q13 is associated with atopic dermatitis. NHGRI|-1
NM_001128925 CYP2C18 19578179 http://www.ncbi.nlm.nih.gov/pubmed/19578179 Acenocoumarol rs12772169 8.00E-12 A genome-wide association study of acenocoumarol maintenance dosage. NHGRI|-1
NM_001128925 CYP2C18 19706858 http://www.ncbi.nlm.nih.gov/pubmed/19706858 Ticlopidine rs12777823 2.00E-13 Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy. NHGRI|-1
NM_001128929 ROBO2 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs9836484 4.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_001128929 ROBO2 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs9831754 8.00E-06 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_001128929 ROBO2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Glycoproteins rs9834373 4.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001128931 NAF1 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs6840361 4.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001129758 DPEP3 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, HDL" rs255049 3.00E-08 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001129758 DPEP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs255049 3.06E-08 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_001129827 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129827 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129827 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129827 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129829 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129829 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129829 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129829 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129830 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129830 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129830 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129830 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129831 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129831 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129831 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129831 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129832 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129832 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129832 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129832 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129833 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129833 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129833 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129833 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129834 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129834 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129834 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129834 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129835 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129835 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129835 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129835 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129836 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129836 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129836 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129836 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129837 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129837 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129837 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129837 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129838 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129838 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129838 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129838 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129839 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129839 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129839 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129839 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129840 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129840 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129840 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129840 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129841 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129841 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129841 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129841 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129842 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129842 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129842 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129842 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129843 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129843 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129843 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129843 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129844 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129844 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129844 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129844 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129846 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001129846 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001129846 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001129846 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001129890 LRRC69 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4609161 5.18E-06 NBL-GWAS version 2 dbGaP|2895
NM_001129891 FAM196B 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs259892 1.10E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001129994 KCTD15 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs29941 3.00E-09 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001129994 KCTD15 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs29941 7.00E-12 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001129994 KCTD15 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs29941 5.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001129994 KCTD15 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs11084753 2.00E-08 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_001129995 KCTD15 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs29941 3.00E-09 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001129995 KCTD15 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs29941 7.00E-12 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001129995 KCTD15 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs29941 5.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001129995 KCTD15 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs11084753 2.00E-08 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_001130004 ACTN1 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs2268983 7.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001130005 ACTN1 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs2268983 7.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001130015 ANKRD33 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs17126180 9.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001130033 PLEKHB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs593927 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001130034 PLEKHB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs593927 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001130035 PLEKHB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs593927 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001130036 PLEKHB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs593927 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001130037 ELMOD1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Personality rs10431058 8.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001130046 CCL20 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs7591163 3.00E-07 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001130058 SLC44A5 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs1857353 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001130064 GAP43 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4831199 1.07E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001130064 GAP43 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11926976 7.10E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001130067 TRIM2 21654844 http://www.ncbi.nlm.nih.gov/pubmed/21654844 Multiple Sclerosis rs12644284 4.00E-06 Genome-wide association study of severity in multiple sclerosis. NHGRI|-1
NM_001130081 PLD1 21701570 http://www.ncbi.nlm.nih.gov/pubmed/21701570 Body Mass Index rs6794092 2.00E-06 Genome-Wide Association of BMI in African Americans. NHGRI|-1
NM_001130101 NR1H3 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, HDL" rs7120118 4.00E-08 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001130101 NR1H3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs7120118 3.57E-08 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_001130102 NR1H3 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, HDL" rs7120118 4.00E-08 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001130102 NR1H3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs7120118 3.57E-08 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_001130103 COL13A1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs7077164 7.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001130103 COL13A1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1227756 2.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001130110 SETBP1 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs991014 6.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001130110 SETBP1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs616444 9.00E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001130110 SETBP1 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs2243803 3.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001130110 SETBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6507618 7.92E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001130110 SETBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs8099273 6.66E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001130110 SETBP1 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Albumins rs10502868 7.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001130112 RFC5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7295696 1.77E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001130113 RFC5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7295696 1.77E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001130140 ERAP2 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs2549794 1.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001130141 PCBP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2839020 6.58E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130141 PCBP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9976523 7.46E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001130141 PCBP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs9980967 2.07E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001130141 PCBP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11701130 2.79E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130141 PCBP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4819143 7.47E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130142 VWA5A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs880321 7.55E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001130145 YAP1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs2852894 1.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001130156 MLF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1714524 1.36E-05 NBL-GWAS version 2 dbGaP|2895
NM_001130156 MLF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1656377 4.94E-05 NBL-GWAS version 2 dbGaP|2895
NM_001130157 MLF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1714524 1.36E-05 NBL-GWAS version 2 dbGaP|2895
NM_001130157 MLF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1656377 4.94E-05 NBL-GWAS version 2 dbGaP|2895
NM_001130172 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs7775698 1.00E-14 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001130172 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs7775698 1.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001130172 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-56 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001130172 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-66 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001130172 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 5.00E-13 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001130172 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 8.00E-18 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001130172 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7776054 7.00E-69 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001130172 MYB 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs9399137 3.00E-36 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_001130172 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Platelet Count rs9399137 1.00E-09 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001130172 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9373124 7.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001130172 MYB 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs9373124 1.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001130172 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4895441 7.00E-86 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001130172 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs4895441 2.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001130172 MYB 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs9376092 2.00E-11 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_001130172 MYB 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9402686 7.00E-42 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001130172 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs9494145 3.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001130172 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Count rs9483788 1.00E-47 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001130172 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs9483788 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001130172 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 1.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001130172 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 3.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001130172 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 6.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001130173 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs7775698 1.00E-14 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001130173 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs7775698 1.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001130173 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-56 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001130173 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-66 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001130173 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 5.00E-13 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001130173 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 8.00E-18 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001130173 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7776054 7.00E-69 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001130173 MYB 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs9399137 3.00E-36 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_001130173 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Platelet Count rs9399137 1.00E-09 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001130173 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9373124 7.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001130173 MYB 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs9373124 1.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001130173 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4895441 7.00E-86 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001130173 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs4895441 2.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001130173 MYB 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs9376092 2.00E-11 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_001130173 MYB 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9402686 7.00E-42 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001130173 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs9494145 3.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001130173 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Count rs9483788 1.00E-47 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001130173 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs9483788 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001130173 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 1.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001130173 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 3.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001130173 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 6.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001130182 DNAJA4 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Exploratory Behavior rs1533665 7.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_001130183 DNAJA4 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Exploratory Behavior rs1533665 7.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_001130404 PRR20A 20833655 http://www.ncbi.nlm.nih.gov/pubmed/20833655 Warfarin rs1512651 6.00E-06 Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. NHGRI|-1
NM_001130405 PRR20A 20833655 http://www.ncbi.nlm.nih.gov/pubmed/20833655 Warfarin rs1512651 6.00E-06 Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. NHGRI|-1
NM_001130406 PRR20A 20833655 http://www.ncbi.nlm.nih.gov/pubmed/20833655 Warfarin rs1512651 6.00E-06 Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. NHGRI|-1
NM_001130407 PRR20A 20833655 http://www.ncbi.nlm.nih.gov/pubmed/20833655 Warfarin rs1512651 6.00E-06 Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. NHGRI|-1
NM_001130417 SLC8A3 21602797 http://www.ncbi.nlm.nih.gov/pubmed/21602797 Cystic Fibrosis rs12883884 8.00E-06 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. NHGRI|-1
NM_001130455 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001130480 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1016771 1.26E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130480 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2043890 1.53E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130480 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2717055 4.33E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130480 VRK2 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs2312147 3.00E-07 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_001130481 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1016771 1.26E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130481 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2043890 1.53E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130481 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2717055 4.33E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130481 VRK2 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs2312147 3.00E-07 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_001130482 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1016771 1.26E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130482 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2043890 1.53E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130482 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2717055 4.33E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130482 VRK2 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs2312147 3.00E-07 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_001130483 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1016771 1.26E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130483 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2043890 1.53E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130483 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2717055 4.33E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001130483 VRK2 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs2312147 3.00E-07 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_001130518 CSGALNACT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6983139 2.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001130518 CSGALNACT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6983139 5.10E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001130524 AP1M1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12185505 3.68E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001130675 CLGN 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Bilirubin rs1594468 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001130690 PDE10A 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs475061 1.23E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001130690 PDE10A 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs7762160 1.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001130690 PDE10A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1389923 7.18E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001130691 PPP3CA 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Piperazines rs1405687 5.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001130692 PPP3CA 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Piperazines rs1405687 5.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001130709 RUFY3 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7686646 9.64E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001130709 RUFY3 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs6815629 9.64E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001130713 LEF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17038960 3.00E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001130714 LEF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17038960 3.00E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001130720 AHCYL2 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs7787531 9.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_001130721 ELOVL6 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs10011926 8.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_001130722 AHCYL2 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs7787531 9.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_001130723 AHCYL2 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs7787531 9.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_001130845 BCL6 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Blood Urea Nitrogen rs9820070 1.00E-11 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001130851 CDKN3 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs4293296 3.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001130860 HEPH 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs5965182 6.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001130863 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7000665 1.12E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001130863 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9643136 1.15E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001130863 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6993464 6.39E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001130863 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11782176 5.55E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001130863 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6991756 5.01E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001130865 DMRT2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs17641078 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001130910 CCRL2 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs1015164 9.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_001130910 CCRL2 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs6441975 5.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_001130915 MAMSTR 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs281379 7.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001130918 TTLL6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs8073596 7.62E-05 NBL-GWAS version 2 dbGaP|2895
NM_001130976 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001130977 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001130978 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001130979 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001130980 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001130981 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001130982 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001130983 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001130984 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001130985 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001130986 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001130987 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001130996 HMGCR 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs12654264 1.00E-20 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_001130996 HMGCR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs3846662 2.00E-11 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001130996 HMGCR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs3846662 3.00E-19 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001130996 HMGCR 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 "Cholesterol, LDL" rs3846663 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001130996 HMGCR 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs3846663 8.00E-12 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001130996 HMGCR 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Cholesterol rs3846663 6.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001130996 HMGCR 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs12916 1.00E-11 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001130996 HMGCR 18802019 http://www.ncbi.nlm.nih.gov/pubmed/18802019 "Cholesterol, LDL" rs7703051 1.00E-08 Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. NHGRI|-1
NM_001131005 MEF2C 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs770189 3.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001131005 MEF2C 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs10037512 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001131005 MEF2C 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1366594 1.00E-13 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001131005 MEF2C 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs1366594 1.00E-07 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_001131005 MEF2C 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs1366594 8.00E-10 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_001131005 MEF2C 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs12518099 7.00E-07 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001131005 MEF2C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2972956 6.07E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001131005 MEF2C 21060863 http://www.ncbi.nlm.nih.gov/pubmed/21060863 Retinal Vein rs17421627 7.00E-16 "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo." NHGRI|-1
NM_001131010 SATB1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs6792314 8.60E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001131010 SATB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11914608 1.42E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001131010 SATB1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs13073817 7.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001131010 SATB1 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs6809854 1.00E-07 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_001131027 PDLIM4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4594848 7.35E-05 NBL-GWAS version 2 dbGaP|2895
NM_001131034 RNF212 18239089 http://www.ncbi.nlm.nih.gov/pubmed/18239089 "Recombination, Genetic" rs1670533 2.00E-12 Sequence variants in the RNF212 gene associate with genome-wide recombination rate. NHGRI|-1
NM_001131034 RNF212 18239089 http://www.ncbi.nlm.nih.gov/pubmed/18239089 "Recombination, Genetic" rs3796619 3.00E-24 Sequence variants in the RNF212 gene associate with genome-wide recombination rate. NHGRI|-1
NM_001131034 RNF212 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6839931 2.09E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001131034 RNF212 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7669622 4.53E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001131034 RNF212 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6827357 5.15E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001134222 IRX2 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs12653946 4.00E-18 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_001134222 IRX2 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs6879627 8.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_001134222 IRX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs370672 6.66E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001134223 USP46 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Triglycerides rs346923 2.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001134233 C1orf204 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs2501354 8.08E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001134285 ESRRG 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs12757165 1.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001134285 ESRRG 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs1436900 7.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_001134285 ESRRG 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs1497828 4.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001134367 SLC6A6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9834678 5.65E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001134367 SLC6A6 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs9036 3.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001134368 SLC6A6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9834678 5.65E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001134368 SLC6A6 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs9036 3.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001134373 NT5C2 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs11191548 4.00E-17 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_001134373 NT5C2 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs11191548 7.00E-12 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_001134373 NT5C2 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs11191548 7.00E-24 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_001134382 IQSEC1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs765248 1.04E-04 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001134395 C7orf50 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs10256972 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001134396 C7orf50 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs10256972 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001134398 VAV2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2810545 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001134398 VAV2 20598377 http://www.ncbi.nlm.nih.gov/pubmed/20598377 Multiple Sclerosis rs3780792 1.00E-06 Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. NHGRI|-1
NM_001134407 GRIN2A 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs8050385 1.90E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001134407 GRIN2A 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs1463132 8.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001134407 GRIN2A 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs17550532 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001134408 GRIN2A 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs8050385 1.90E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001134408 GRIN2A 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs1463132 8.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001134408 GRIN2A 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs17550532 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001134418 LEPREL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs16865151 1.71E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001134418 LEPREL1 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs16865258 2.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001134418 LEPREL1 18794855 http://www.ncbi.nlm.nih.gov/pubmed/18794855 Urinary Bladder Neoplasms rs710521 1.00E-07 Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001134418 LEPREL1 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs710521 2.00E-10 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_001134418 LEPREL1 20348956 http://www.ncbi.nlm.nih.gov/pubmed/20348956 Urinary Bladder Neoplasms rs710521 6.00E-08 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001134434 SPOCK2 21216879 http://www.ncbi.nlm.nih.gov/pubmed/21216879 Insulin-Like Growth Factor I rs1245541 5.00E-07 A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. NHGRI|-1
NM_001134445 DDAH1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1523993 6.03E-05 NBL-GWAS version 2 dbGaP|2895
NM_001134470 C3orf58 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs800082 3.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001134470 C3orf58 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Prostatic Neoplasms rs345013 5.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001134477 PARN 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1659127 4.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001134479 LRRC8D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1215582 8.52E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001134492 HS2ST1 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs7553864 3.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001134492 HS2ST1 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Eosinophils rs6576878 6.00E-06 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001134649 EIF4E3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10460943 7.33E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001134650 EIF4E3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10460943 7.33E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001134651 EIF4E3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10460943 7.33E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001134659 PRR23A 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs1511412 2.00E-13 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_001134663 SAMD13 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs1085093 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001134664 SAMD13 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs1085093 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001134672 C10orf84 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11198446 7.49E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001134673 NFIA 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs6691768 1.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001134673 NFIA 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9436640 5.00E-18 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001134673 NFIA 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs2989476 3.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_001134673 NFIA 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs472913 2.00E-07 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001134734 C1orf94 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2994598 3.11E-06 NBL-GWAS version 1 dbGaP|2845
NM_001134734 C1orf94 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs10914952 1.64E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001134734 C1orf94 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2359631 6.37E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001134734 C1orf94 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs612353 9.05E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001134738 BCL6 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Blood Urea Nitrogen rs9820070 1.00E-11 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001134745 LRRTM4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1921246 5.63E-06 NBL-GWAS version 1 dbGaP|2845
NM_001134745 LRRTM4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs17012789 4.44E-06 NBL-GWAS version 1 dbGaP|2845
NM_001134778 PBX3 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs888219 2.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001134888 RTL1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs3825569 3.69E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001135 ACAN 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs8041863 8.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001135031 GFI1B 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs2905072 6.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001135037 MFAP3 21701570 http://www.ncbi.nlm.nih.gov/pubmed/21701570 Body Mass Index rs2033195 6.00E-06 Genome-Wide Association of BMI in African Americans. NHGRI|-1
NM_001135047 JDP2 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs7155603 1.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001135048 JDP2 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs7155603 1.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001135049 JDP2 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs7155603 1.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001135052 SYK 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic Nephropathies rs773506 6.00E-06 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_001135055 TKT 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs4687718 6.00E-09 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001135098 UPP2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10183640 5.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001135101 CRELD2 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs28372448 8.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_001135109 RIC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4758051 2.83E-08 NBL-GWAS version 2 dbGaP|2895
NM_001135109 RIC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10840002 6.01E-06 NBL-GWAS version 2 dbGaP|2895
NM_001135111 KCNK17 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2395721 5.53E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001135111 KCNK17 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs9471058 5.65E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001135111 KCNK17 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10807204 6.70E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001135146 SLC39A8 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs13107325 2.00E-13 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001135147 SLC39A8 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs13107325 2.00E-13 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001135148 SLC39A8 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs13107325 2.00E-13 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001135155 DPF1 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs8102476 2.00E-11 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_001135156 DPF1 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs8102476 2.00E-11 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_001135170 C1QTNF7 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs16891867 3.00E-09 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001135170 C1QTNF7 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1861046 6.00E-08 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001135171 C1QTNF7 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs16891867 3.00E-09 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001135171 C1QTNF7 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1861046 6.00E-08 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001135190 ARAP1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs1552224 1.00E-22 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001135191 ASAP2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1109670 9.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001135196 C10orf71 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs4838508 2.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001135211 FKBP6 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17339199 4.21E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001135213 GIT2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs2292354 7.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001135213 GIT2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11068997 7.24E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001135214 GIT2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs2292354 7.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001135214 GIT2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11068997 7.24E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001135215 ZNF323 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs853679 2.52E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001135215 ZNF323 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs853676 5.22E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001135215 ZNF323 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs853676 6.14E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001135216 ZNF323 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs853679 2.52E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001135216 ZNF323 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs853676 5.22E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001135216 ZNF323 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs853676 6.14E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001135239 LDHA 21124955 http://www.ncbi.nlm.nih.gov/pubmed/21124955 Serum Amyloid A Protein rs2896526 4.00E-22 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. NHGRI|-1
NM_001135247 MFAP2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2284746 4.00E-29 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001135248 MFAP2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2284746 4.00E-29 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001135254 PAX7 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs12063142 5.00E-07 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_001135564 HSF2 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs9398652 4.00E-15 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_001135564 HSF2 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Heart Rate rs12110693 2.00E-09 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001135590 ZNF577 21424380 http://www.ncbi.nlm.nih.gov/pubmed/21424380 Breast Neoplasms rs10411161 7.00E-06 Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility. NHGRI|-1
NM_001135599 TGFB2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1018040 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001135599 TGFB2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1018040 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001135602 GLB1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs13314993 3.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001135602 GLB1 21105107 http://www.ncbi.nlm.nih.gov/pubmed/21105107 "Carcinoma, Hepatocellular" rs4678680 2.00E-07 Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma. NHGRI|-1
NM_001135604 ESM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4865879 6.81E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001135604 ESM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10940434 3.27E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001135608 ARHGAP26 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs27779 2.53E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001135608 ARHGAP26 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs245852 6.94E-05 NBL-GWAS version 2 dbGaP|2895
NM_001135608 ARHGAP26 18759275 http://www.ncbi.nlm.nih.gov/pubmed/18759275 Uric Acid rs3776331 8.00E-06 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. NHGRI|-1
NM_001135610 PRDM2 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs2245218 2.13E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001135639 CNGB1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs3784900 6.67E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001135639 CNGB1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs3784901 5.51E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001135648 PTPRK 20068591 http://www.ncbi.nlm.nih.gov/pubmed/20068591 Hearing Loss rs10499138 2.00E-06 A genome-wide association study for age-related hearing impairment in the Saami. NHGRI|-1
NM_001135648 PTPRK 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs802734 3.00E-14 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001135659 NRXN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10196324 6.42E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001135659 NRXN1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs1356888 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001135659 NRXN1 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Exploratory Behavior rs10176705 9.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_001135659 NRXN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs991902 3.48E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001135659 NRXN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2839839 7.09E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001135659 NRXN1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1156742 8.14E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001135662 RAB7L1 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson Disease rs947211 2.00E-12 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_001135663 RAB7L1 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson Disease rs947211 2.00E-12 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_001135664 RAB7L1 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson Disease rs947211 2.00E-12 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_001135670 MSRA 21679298 http://www.ncbi.nlm.nih.gov/pubmed/21679298 Schizophrenia rs7017212 4.00E-06 A genome-wide association study for quantitative traits in schizophrenia in China. NHGRI|-1
NM_001135670 MSRA 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs11775334 4.00E-06 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001135670 MSRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6992153 9.14E-05 NBL-GWAS version 2 dbGaP|2895
NM_001135670 MSRA 20452100 http://www.ncbi.nlm.nih.gov/pubmed/20452100 Neurofibrillary Tangles rs11782819 3.00E-06 Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study. NHGRI|-1
NM_001135670 MSRA 19557161 http://www.ncbi.nlm.nih.gov/pubmed/19557161 Adiposity rs545854 9.00E-09 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. NHGRI|-1
NM_001135670 MSRA 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs545854 3.57E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001135671 MSRA 21679298 http://www.ncbi.nlm.nih.gov/pubmed/21679298 Schizophrenia rs7017212 4.00E-06 A genome-wide association study for quantitative traits in schizophrenia in China. NHGRI|-1
NM_001135671 MSRA 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs11775334 4.00E-06 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001135671 MSRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6992153 9.14E-05 NBL-GWAS version 2 dbGaP|2895
NM_001135671 MSRA 20452100 http://www.ncbi.nlm.nih.gov/pubmed/20452100 Neurofibrillary Tangles rs11782819 3.00E-06 Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study. NHGRI|-1
NM_001135671 MSRA 19557161 http://www.ncbi.nlm.nih.gov/pubmed/19557161 Adiposity rs545854 9.00E-09 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. NHGRI|-1
NM_001135671 MSRA 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs545854 3.57E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001135674 C8orf40 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs6474412 1.00E-08 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_001135675 C8orf40 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs6474412 1.00E-08 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_001135676 C8orf40 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs6474412 1.00E-08 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_001135699 YWHAZ 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3491 1.79E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001135699 YWHAZ 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs931812 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001135700 YWHAZ 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3491 1.79E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001135700 YWHAZ 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs931812 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001135701 YWHAZ 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3491 1.79E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001135701 YWHAZ 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs931812 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001135702 YWHAZ 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3491 1.79E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001135702 YWHAZ 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs931812 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001135703 LRP12 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs16872085 1.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001135703 LRP12 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Benzodiazepines rs977396 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001135704 ACBD4 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs12946454 1.00E-08 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_001135704 ACBD4 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs4986172 2.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001135705 ACBD4 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs12946454 1.00E-08 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_001135705 ACBD4 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs4986172 2.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001135706 ACBD4 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs12946454 1.00E-08 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_001135706 ACBD4 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs4986172 2.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001135707 ACBD4 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs12946454 1.00E-08 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_001135707 ACBD4 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs4986172 2.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001135731 ZMAT4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2122950 2.02E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001135731 ZMAT4 17903298 http://www.ncbi.nlm.nih.gov/pubmed/17903298 Blood Glucose rs2722425 2.00E-08 Genome-wide association with diabetes-related traits in the Framingham Heart Study. NHGRI|-1
NM_001135731 ZMAT4 17903298 http://www.ncbi.nlm.nih.gov/pubmed/17903298 Blood Glucose rs2722425 9.00E-06 Genome-wide association with diabetes-related traits in the Framingham Heart Study. NHGRI|-1
NM_001135731 ZMAT4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4736788 4.88E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001135731 ZMAT4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10094981 4.82E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001135731 ZMAT4 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs11786458 9.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001135733 TP53INP1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs896854 1.00E-09 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001135746 NEIL2 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs6601606 1.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001135747 NEIL2 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs6601606 1.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001135748 NEIL2 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs6601606 1.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001135765 ATP2A2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Alpha-Globulins rs11065611 1.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001135771 RPN2 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs6031882 6.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_001135773 SPATA2 18364390 http://www.ncbi.nlm.nih.gov/pubmed/18364390 Psoriasis rs495337 1.00E-08 Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene. NHGRI|-1
NM_001135773 SPATA2 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs495337 2.00E-07 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_001135774 SYN3 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs9621532 1.00E-11 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_001135774 SYN3 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs9621532 2.00E-15 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001135774 SYN3 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs9621532 4.00E-09 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_001135775 C9orf7 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs4962153 8.00E-21 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_001135775 C9orf7 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs4962153 8.05E-14 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001135775 C9orf7 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs739468 2.79E-14 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001135775 C9orf7 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs3094379 2.93E-13 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001135776 ZBTB43 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs867559 1.00E-07 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001135823 SSPN 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs718314 2.00E-17 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001135863 C12orf72 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs12579938 1.00E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001135864 C12orf72 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs12579938 1.00E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001135919 SLC46A3 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1305088 9.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001135920 KIAA1432 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7026868 6.90E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001135920 KIAA1432 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs4740820 6.41E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001135934 POSTN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1324038 2.34E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001135934 POSTN 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs1590305 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001135935 POSTN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1324038 2.34E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001135935 POSTN 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs1590305 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001135936 POSTN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1324038 2.34E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001135936 POSTN 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs1590305 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001135943 MADD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs4752977 9.72E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_001135943 MADD 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs7944584 2.00E-18 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001135944 MADD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs4752977 9.72E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_001135944 MADD 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs7944584 2.00E-18 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001135955 TRPC4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs17210569 3.59E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001135956 TRPC4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs17210569 3.59E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001135957 TRPC4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs17210569 3.59E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001135958 TRPC4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs17210569 3.59E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001136 AGER 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs8365 1.09E-17 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001136 AGER 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs2070600 3.00E-14 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001136 AGER 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs2070600 3.00E-15 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_001136 AGER 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs2070600 2.18E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_001136005 GART 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8971 6.96E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001136005 GART 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2834232 6.96E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001136006 GART 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8971 6.96E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001136006 GART 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2834232 6.96E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001136017 CCND3 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Count rs3218097 1.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001136017 CCND3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9349205 1.00E-31 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001136017 CCND3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9349205 8.00E-20 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001136017 CCND3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs11970772 7.00E-19 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001136017 CCND3 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs11968166 8.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001136021 NFATC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2143630 7.41E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001136022 NFATC4 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs1950500 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001136023 NFE2 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs10506328 5.00E-07 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001136029 DEPDC5 21725309 http://www.ncbi.nlm.nih.gov/pubmed/21725309 "Hepatitis C, Chronic" rs1012068 1.00E-13 Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers. NHGRI|-1
NM_001136034 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7730742 9.29E-05 NBL-GWAS version 2 dbGaP|2895
NM_001136034 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10035707 5.09E-05 NBL-GWAS version 2 dbGaP|2895
NM_001136034 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs957459 4.21E-05 NBL-GWAS version 2 dbGaP|2895
NM_001136034 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2619046 1.76E-05 NBL-GWAS version 2 dbGaP|2895
NM_001136034 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs162096 3.33E-05 NBL-GWAS version 2 dbGaP|2895
NM_001136051 LRIG3 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs11172782 7.00E-08 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_001136053 TPRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11915684 3.50E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001136053 TPRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4679351 1.81E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001136053 TPRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6809319 2.64E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001136053 TPRA1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs9871760 4.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001136053 TPRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs9871760 4.12E-05 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_001136103 TMEM132C 21423239 http://www.ncbi.nlm.nih.gov/pubmed/21423239 "Suicide, Attempted" rs7296262 1.00E-06 A genome-wide association study of attempted suicide. NHGRI|-1
NM_001136103 TMEM132C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10773566 1.68E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001136103 TMEM132C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10773566 7.52E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001136103 TMEM132C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1489430 5.09E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001136103 TMEM132C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6486717 6.89E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001136103 TMEM132C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4765114 4.61E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001136103 TMEM132C 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs950795 8.00E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001136103 TMEM132C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10847282 1.39E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001136103 TMEM132C 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs1823172 5.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001136103 TMEM132C 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs10744304 9.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_001136105 C11orf93 18372901 http://www.ncbi.nlm.nih.gov/pubmed/18372901 Colorectal Neoplasms rs3802842 6.00E-10 Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. NHGRI|-1
NM_001136125 CCND3 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Count rs3218097 1.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001136125 CCND3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9349205 1.00E-31 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001136125 CCND3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9349205 8.00E-20 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001136125 CCND3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs11970772 7.00E-19 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001136125 CCND3 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs11968166 8.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001136126 CCND3 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Count rs3218097 1.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001136126 CCND3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9349205 1.00E-31 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001136126 CCND3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9349205 8.00E-20 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001136126 CCND3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs11970772 7.00E-19 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001136126 CCND3 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs11968166 8.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001136127 DNM3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs10914144 2.00E-14 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001136127 DNM3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs678962 3.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001136127 DNM3 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs1011731 1.00E-17 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001136154 ERG 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs7275212 2.00E-18 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001136154 ERG 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2836496 7.04E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001136154 ERG 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2836505 5.78E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001136154 ERG 20662065 http://www.ncbi.nlm.nih.gov/pubmed/20662065 Lupus Vulgaris rs743446 5.00E-06 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. NHGRI|-1
NM_001136155 ERG 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs7275212 2.00E-18 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001136155 ERG 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2836496 7.04E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001136155 ERG 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2836505 5.78E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001136155 ERG 20662065 http://www.ncbi.nlm.nih.gov/pubmed/20662065 Lupus Vulgaris rs743446 5.00E-06 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. NHGRI|-1
NM_001136156 ZNF507 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2867743 1.84E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001136193 FASTKD2 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs2277912 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001136194 FASTKD2 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs2277912 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001136195 TNPO2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs722571 8.62E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001136196 TNPO2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs722571 8.62E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001136200 C10orf32 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs3824754 3.92E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001136200 C10orf32 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11191425 3.96E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001136205 KCTD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs6508445 7.37E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001136205 KCTD1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs16942421 8.00E-10 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001136219 FCGR2A 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 "Colitis, Ulcerative" rs1801274 2.00E-12 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_001136219 FCGR2A 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs1801274 2.00E-20 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001136219 FCGR2A 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs10800309 3.00E-09 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_001136239 PRDM6 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs17470137 1.00E-11 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_001136469 TMEM108 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs13072106 8.71E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001136469 TMEM108 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1197313 8.95E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001136469 TMEM108 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs6439371 1.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001136469 TMEM108 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs2369955 2.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_001136472 LITAF 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7203193 3.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001136472 LITAF 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs8049607 5.00E-15 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001136472 LITAF 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs8049607 6.00E-15 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001136473 LITAF 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7203193 3.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001136473 LITAF 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs8049607 5.00E-15 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001136473 LITAF 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs8049607 6.00E-15 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001136508 C1orf185 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs17391905 3.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001136534 TMEM233 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7310266 5.81E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001136534 TMEM233 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Exercise Test rs7137869 6.00E-07 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_001136534 TMEM233 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1918416 4.88E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001136536 DTHD1 20802204 http://www.ncbi.nlm.nih.gov/pubmed/20802204 Multiple Sclerosis rs13117816 7.00E-06 Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. NHGRI|-1
NM_001136538 ACAD10 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs11066015 7.00E-21 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001136540 APOL1 20668430 http://www.ncbi.nlm.nih.gov/pubmed/20668430 "Glomerulosclerosis, Focal Segmental" rs2239785 5.00E-13 A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. NHGRI|-1
NM_001136541 APOL1 20668430 http://www.ncbi.nlm.nih.gov/pubmed/20668430 "Glomerulosclerosis, Focal Segmental" rs2239785 5.00E-13 A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. NHGRI|-1
NM_001136562 AKAP2 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs7032940 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001136566 RAD21L1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs397020 8.00E-07 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001136570 FAM47E 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs6812193 4.00E-07 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_001136570 FAM47E 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs6812193 8.00E-10 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_001139443 BEST1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2668898 5.65E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001139466 TBL1X 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1024443 6.38E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001139467 TBL1X 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1024443 6.38E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001139468 TBL1X 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1024443 6.38E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001139488 RASGRP3 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs13385731 1.00E-15 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_001139514 DACH2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs242849 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001139515 DACH2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs242849 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001141917 C9orf144B 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs951005 4.00E-10 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001141945 ACTA2 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs1926203 1.00E-06 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_001141947 CCDC66 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs2054989 6.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001141972 ATPBD4 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1510385 1.43E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001141972 ATPBD4 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs4923705 2.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_001141972 ATPBD4 20673876 http://www.ncbi.nlm.nih.gov/pubmed/20673876 "Depressive Disorder, Major" rs10520045 7.00E-06 "Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression." NHGRI|-1
NM_001141972 ATPBD4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs16962759 6.38E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001141972 ATPBD4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs16962759 8.28E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001141972 ATPBD4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4130461 4.52E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001141972 ATPBD4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs8028529 1.51E-06 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001141972 ATPBD4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4459505 1.12E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001141973 ATP13A2 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs3738814 2.00E-07 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001141974 ATP13A2 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs3738814 2.00E-07 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001141979 TP53BP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2439832 9.27E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001141980 TP53BP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2439832 9.27E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001142279 RNASEH2B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2408213 5.24E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001142282 RPS24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1916400 1.80E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142282 RPS24 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs2395528 6.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001142282 RPS24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs35648 3.27E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142283 RPS24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1916400 1.80E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142283 RPS24 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs2395528 6.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001142283 RPS24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs35648 3.27E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142284 RPS24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1916400 1.80E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142284 RPS24 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs2395528 6.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001142284 RPS24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs35648 3.27E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142285 RPS24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1916400 1.80E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142285 RPS24 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs2395528 6.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001142285 RPS24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs35648 3.27E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142292 LMAN2L 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs2314398 3.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001142298 SQSTM1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10516140 6.02E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001142299 SQSTM1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10516140 6.02E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001142315 LMO2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4756052 3.29E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001142316 LMO2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4756052 3.29E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001142326 DMTF1 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs11773103 1.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001142327 DMTF1 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs11773103 1.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001142333 RBFOX1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs6500744 3.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001142333 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13336322 9.10E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001142333 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7188257 7.46E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001142333 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4786850 3.70E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001142333 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17822719 2.54E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001142333 RBFOX1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit Disorder with Hyperactivity rs12921846 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001142333 RBFOX1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1551960 4.67E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001142333 RBFOX1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs899305 6.31E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001142333 RBFOX1 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Nonalcoholic Fatty Liver Disease rs9302841 2.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_001142333 RBFOX1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs4787008 6.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001142333 RBFOX1 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Phosphatidylcholines rs9924951 5.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_001142334 RBFOX1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs6500744 3.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001142334 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13336322 9.10E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001142334 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7188257 7.46E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001142334 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4786850 3.70E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001142334 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17822719 2.54E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001142334 RBFOX1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit Disorder with Hyperactivity rs12921846 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001142334 RBFOX1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1551960 4.67E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001142334 RBFOX1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs899305 6.31E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001142334 RBFOX1 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Nonalcoholic Fatty Liver Disease rs9302841 2.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_001142334 RBFOX1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs4787008 6.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001142334 RBFOX1 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Phosphatidylcholines rs9924951 5.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_001142339 GNAL 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10468679 1.72E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001142343 CMKLR1 21483023 http://www.ncbi.nlm.nih.gov/pubmed/21483023 Response to platinum-based chemotherapy in non-small-cell lung cancer rs1878022 5.00E-07 Genome-wide association study of survival in non-small cell lung cancer patients receiving platinum-based chemotherapy. NHGRI|-1
NM_001142343 CMKLR1 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs10861905 8.00E-07 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001142344 CMKLR1 21483023 http://www.ncbi.nlm.nih.gov/pubmed/21483023 Response to platinum-based chemotherapy in non-small-cell lung cancer rs1878022 5.00E-07 Genome-wide association study of survival in non-small cell lung cancer patients receiving platinum-based chemotherapy. NHGRI|-1
NM_001142344 CMKLR1 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs10861905 8.00E-07 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001142345 CMKLR1 21483023 http://www.ncbi.nlm.nih.gov/pubmed/21483023 Response to platinum-based chemotherapy in non-small-cell lung cancer rs1878022 5.00E-07 Genome-wide association study of survival in non-small cell lung cancer patients receiving platinum-based chemotherapy. NHGRI|-1
NM_001142345 CMKLR1 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs10861905 8.00E-07 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001142389 PNPLA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs5934349 1.75E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142393 NEDD9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11751998 6.75E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001142397 KIAA0427 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs8091345 1.38E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001142397 KIAA0427 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs9952724 2.28E-10 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001142414 CRCP 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs875971 4.00E-06 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_001142415 AIMP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4956263 6.74E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001142415 AIMP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4956263 7.90E-06 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001142416 AIMP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4956263 6.74E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001142416 AIMP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4956263 7.90E-06 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001142445 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs6474359 1.00E-08 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_001142445 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs4737009 6.00E-12 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_001142445 ANK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4466386 6.52E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001142446 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs6474359 1.00E-08 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_001142446 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs4737009 6.00E-12 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_001142446 ANK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4466386 6.52E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001142471 INTS12 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs11727189 5.00E-17 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001142474 C5orf13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs173896 5.04E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142475 C5orf13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs173896 5.04E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142476 C5orf13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs173896 5.04E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142477 C5orf13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs173896 5.04E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142478 C5orf13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs173896 5.04E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142479 C5orf13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs173896 5.04E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142480 C5orf13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs173896 5.04E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142481 C5orf13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs173896 5.04E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142482 C5orf13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs173896 5.04E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142483 C5orf13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs173896 5.04E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001142497 MLKL 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7196369 2.05E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001142522 FBXO5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs546599 2.19E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001142549 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7730742 9.29E-05 NBL-GWAS version 2 dbGaP|2895
NM_001142549 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10035707 5.09E-05 NBL-GWAS version 2 dbGaP|2895
NM_001142549 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs957459 4.21E-05 NBL-GWAS version 2 dbGaP|2895
NM_001142549 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2619046 1.76E-05 NBL-GWAS version 2 dbGaP|2895
NM_001142549 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs162096 3.33E-05 NBL-GWAS version 2 dbGaP|2895
NM_001142552 DCHS2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs12649437 2.20E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001142553 DCHS2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs12649437 2.20E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001142568 BBX 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs6437740 2.00E-07 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001142568 BBX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7610766 7.23E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001142568 BBX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1850344 4.72E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001142568 BBX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10511260 3.41E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001142569 C1orf106 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs7554511 1.00E-06 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_001142569 C1orf106 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs7554511 2.00E-13 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001142587 NFYC 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4660456 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001142588 NFYC 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4660456 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001142589 NFYC 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4660456 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001142590 NFYC 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4660456 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001142598 P4HA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4594848 7.35E-05 NBL-GWAS version 2 dbGaP|2895
NM_001142599 P4HA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4594848 7.35E-05 NBL-GWAS version 2 dbGaP|2895
NM_001142610 ULK2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs281357 2.51E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001142614 EHBP1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2710638 4.99E-07 NBL-GWAS version 1 dbGaP|2845
NM_001142614 EHBP1 18264098 http://www.ncbi.nlm.nih.gov/pubmed/18264098 Prostatic Neoplasms rs721048 8.00E-09 Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. NHGRI|-1
NM_001142615 EHBP1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2710638 4.99E-07 NBL-GWAS version 1 dbGaP|2845
NM_001142615 EHBP1 18264098 http://www.ncbi.nlm.nih.gov/pubmed/18264098 Prostatic Neoplasms rs721048 8.00E-09 Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. NHGRI|-1
NM_001142616 EHBP1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2710638 4.99E-07 NBL-GWAS version 1 dbGaP|2845
NM_001142616 EHBP1 18264098 http://www.ncbi.nlm.nih.gov/pubmed/18264098 Prostatic Neoplasms rs721048 8.00E-09 Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. NHGRI|-1
NM_001142621 TGFBRAP1 19754311 http://www.ncbi.nlm.nih.gov/pubmed/19754311 Acquired Immunodeficiency Syndrome rs1020064 7.00E-06 Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). NHGRI|-1
NM_001142626 TSHR 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs17111394 4.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_001142626 TSHR 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs8017455 6.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001142644 SPHKAP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4438469 3.55E-05 NBL-GWAS version 2 dbGaP|2895
NM_001142644 SPHKAP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6760875 2.73E-05 NBL-GWAS version 2 dbGaP|2895
NM_001142644 SPHKAP 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs10200894 1.90E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001142646 TPRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11915684 3.50E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001142646 TPRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4679351 1.81E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001142646 TPRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6809319 2.64E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001142646 TPRA1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs9871760 4.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001142646 TPRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs9871760 4.12E-05 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_001142649 ANO5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12295951 2.04E-05 NBL-GWAS version 2 dbGaP|2895
NM_001142678 ANO6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12579771 2.29E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001142679 ANO6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12579771 2.29E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001142680 ANO6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12579771 2.29E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001142683 CCDC121 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs3749147 1.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001142699 DLG2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Chemokine CCL2 rs3885683 8.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001142699 DLG2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10501570 6.75E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001142699 DLG2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10501570 7.00E-06 Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_001142699 DLG2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs6592199 1.45E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001142699 DLG2 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs1452928 7.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001142699 DLG2 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Body Height rs10898392 3.00E-06 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_001142700 DLG2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Chemokine CCL2 rs3885683 8.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001142700 DLG2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10501570 6.75E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001142700 DLG2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10501570 7.00E-06 Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_001142700 DLG2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs6592199 1.45E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001142700 DLG2 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs1452928 7.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001142700 DLG2 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Body Height rs10898392 3.00E-06 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_001142702 DLG2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Chemokine CCL2 rs3885683 8.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001142702 DLG2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10501570 6.75E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001142702 DLG2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10501570 7.00E-06 Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_001142702 DLG2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs6592199 1.45E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001142702 DLG2 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs1452928 7.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001142702 DLG2 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Body Height rs10898392 3.00E-06 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_001142730 KCTD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs6508445 7.37E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001142730 KCTD1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs16942421 8.00E-10 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001142763 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11004359 5.25E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142763 PCDH15 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs10740609 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001142763 PCDH15 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1916521 5.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001142763 PCDH15 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12412945 5.50E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001142763 PCDH15 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs583012 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001142763 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1932011 8.49E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142763 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9416295 9.93E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142764 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11004359 5.25E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142764 PCDH15 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs10740609 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001142764 PCDH15 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1916521 5.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001142764 PCDH15 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12412945 5.50E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001142764 PCDH15 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs583012 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001142764 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1932011 8.49E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142764 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9416295 9.93E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142765 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11004359 5.25E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142765 PCDH15 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs10740609 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001142765 PCDH15 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1916521 5.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001142765 PCDH15 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12412945 5.50E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001142765 PCDH15 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs583012 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001142765 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1932011 8.49E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142765 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9416295 9.93E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142766 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11004359 5.25E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142766 PCDH15 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs10740609 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001142766 PCDH15 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1916521 5.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001142766 PCDH15 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12412945 5.50E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001142766 PCDH15 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs583012 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001142766 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1932011 8.49E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142766 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9416295 9.93E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142767 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11004359 5.25E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142767 PCDH15 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs10740609 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001142767 PCDH15 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1916521 5.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001142767 PCDH15 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12412945 5.50E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001142767 PCDH15 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs583012 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001142767 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1932011 8.49E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142767 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9416295 9.93E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142768 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11004359 5.25E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142768 PCDH15 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs10740609 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001142768 PCDH15 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1916521 5.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001142768 PCDH15 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12412945 5.50E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001142768 PCDH15 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs583012 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001142768 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1932011 8.49E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142768 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9416295 9.93E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142769 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11004359 5.25E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142769 PCDH15 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs10740609 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001142769 PCDH15 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1916521 5.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001142769 PCDH15 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12412945 5.50E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001142769 PCDH15 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs583012 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001142769 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1932011 8.49E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142769 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9416295 9.93E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142770 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11004359 5.25E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142770 PCDH15 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs10740609 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001142770 PCDH15 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1916521 5.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001142770 PCDH15 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12412945 5.50E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001142770 PCDH15 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs583012 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001142770 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1932011 8.49E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142770 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9416295 9.93E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142771 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11004359 5.25E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142771 PCDH15 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs10740609 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001142771 PCDH15 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1916521 5.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001142771 PCDH15 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12412945 5.50E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001142771 PCDH15 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs583012 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001142771 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1932011 8.49E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142771 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9416295 9.93E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142772 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11004359 5.25E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142772 PCDH15 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs10740609 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001142772 PCDH15 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1916521 5.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001142772 PCDH15 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12412945 5.50E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001142772 PCDH15 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs583012 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001142772 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1932011 8.49E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142772 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9416295 9.93E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142773 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11004359 5.25E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001142773 PCDH15 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs10740609 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001142773 PCDH15 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1916521 5.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001142773 PCDH15 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12412945 5.50E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001142773 PCDH15 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs583012 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001142773 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1932011 8.49E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142773 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9416295 9.93E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001142807 ACOXL 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs17483466 2.00E-10 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NM_001142807 ACOXL 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Monocytes rs7578982 4.00E-07 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001142857 EFCAB1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs12155623 3.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001142857 EFCAB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900238 9.63E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001142883 IP6K3 20558539 http://www.ncbi.nlm.nih.gov/pubmed/20558539 Phosphorus rs9469578 1.00E-11 Common genetic variants associate with serum phosphorus concentration. NHGRI|-1
NM_001142928 LRRC61 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4721 5.03E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001142930 API5 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs1484948 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001142930 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12273344 6.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001142930 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9300039 5.99E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001142930 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9300039 6.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001142930 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs10501281 5.29E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001142930 API5 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs7928165 3.27E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001142930 API5 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs10501293 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001142931 API5 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs1484948 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001142931 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12273344 6.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001142931 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9300039 5.99E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001142931 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9300039 6.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001142931 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs10501281 5.29E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001142931 API5 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs7928165 3.27E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001142931 API5 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs10501293 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001142958 FBXO15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8086078 1.26E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001142958 FBXO15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8086078 3.24E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001142958 FBXO15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3813108 9.00E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001143682 CALCOCO1 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs941184 3.00E-07 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_001143682 CALCOCO1 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs7969151 2.00E-06 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_001143682 CALCOCO1 20460270 http://www.ncbi.nlm.nih.gov/pubmed/20460270 Biliary Atresia rs2120991 9.00E-06 Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. NHGRI|-1
NM_001143688 DIS3L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6494562 9.58E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001143766 ZNF438 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001143766 ZNF438 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11008171 7.96E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001143767 ZNF438 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001143767 ZNF438 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11008171 7.96E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001143768 ZNF438 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001143768 ZNF438 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11008171 7.96E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001143769 ZNF438 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001143769 ZNF438 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11008171 7.96E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001143770 ZNF438 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001143770 ZNF438 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11008171 7.96E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001143771 ZNF438 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001143771 ZNF438 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11008171 7.96E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001143773 FAM13C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10509101 3.95E-05 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_001143779 IFT81 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Alpha-Globulins rs11065611 1.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001143805 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143805 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143805 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001143805 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001143806 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143806 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143806 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001143806 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001143807 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143807 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143807 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001143807 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001143808 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143808 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143808 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001143808 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001143809 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143809 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143809 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001143809 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001143810 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143810 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143810 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001143810 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001143811 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143811 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143811 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001143811 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001143812 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143812 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143812 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001143812 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001143813 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143813 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143813 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001143813 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001143814 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143814 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143814 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001143814 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001143815 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143815 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143815 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001143815 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001143816 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143816 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001143816 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001143816 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001143820 ETS1 20169177 http://www.ncbi.nlm.nih.gov/pubmed/20169177 "Lupus Erythematosus, Systemic" rs1128334 2.00E-11 Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus. NHGRI|-1
NM_001143820 ETS1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs11221332 5.00E-16 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001143820 ETS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs11221064 1.60E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001143820 ETS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7130878 1.66E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001143820 ETS1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs6590322 9.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_001143820 ETS1 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs6590330 2.00E-25 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_001143826 MAPRE2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs595086 7.11E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001143827 MAPRE2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs595086 7.11E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001143830 GAS2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs7111546 2.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001143831 GRM5 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs16914280 3.00E-07 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001143831 GRM5 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs10831496 5.00E-09 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_001143836 NOX4 20801717 http://www.ncbi.nlm.nih.gov/pubmed/20801717 Amyotrophic Lateral Sclerosis rs1488902 3.00E-06 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. NHGRI|-1
NM_001143837 NOX4 20801717 http://www.ncbi.nlm.nih.gov/pubmed/20801717 Amyotrophic Lateral Sclerosis rs1488902 3.00E-06 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. NHGRI|-1
NM_001143839 PDE2A 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs12418204 5.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_001143839 PDE2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs341076 4.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001143839 PDE2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs193170 3.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001143854 RPH3A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs11614063 9.92E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001143854 RPH3A 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs3803064 7.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001143943 EFCAB2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4658673 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001143948 C6orf105 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs6457906 5.45E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_001143964 TBC1D7 17903304 http://www.ncbi.nlm.nih.gov/pubmed/17903304 Cardiovascular Diseases rs499818 7.00E-06 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. NHGRI|-1
NM_001143965 TBC1D7 17903304 http://www.ncbi.nlm.nih.gov/pubmed/17903304 Cardiovascular Diseases rs499818 7.00E-06 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. NHGRI|-1
NM_001143966 TBC1D7 17903304 http://www.ncbi.nlm.nih.gov/pubmed/17903304 Cardiovascular Diseases rs499818 7.00E-06 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. NHGRI|-1
NM_001143970 CDYL 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs73717741 3.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001143971 CDYL 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs73717741 3.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001143981 CHRDL1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs5943057 9.00E-07 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_001143982 CHRDL1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs5943057 9.00E-07 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_001143983 CHRDL1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs5943057 9.00E-07 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_001143998 SEC14L1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs3744064 7.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001143999 SEC14L1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs3744064 7.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001144001 SEC14L1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs3744064 7.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001144033 STOML3 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs9315632 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001144058 NTM 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs1550976 3.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_001144058 NTM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs1550976 5.59E-06 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_001144058 NTM 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs992564 4.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001144059 NTM 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs1550976 3.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_001144059 NTM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs1550976 5.59E-06 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_001144059 NTM 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs992564 4.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001144060 NHSL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17067596 1.44E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001144060 NHSL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4895529 9.24E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001144063 OSBPL5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4758533 4.82E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001144073 CHORDC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10765288 6.55E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001144073 CHORDC1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs12274302 4.00E-07 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001144073 CHORDC1 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Mortality rs1528753 8.00E-08 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_001144073 CHORDC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4483549 1.63E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001144382 PLCL2 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs1372072 2.00E-08 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001144757 SCG5 18372905 http://www.ncbi.nlm.nih.gov/pubmed/18372905 Colorectal Neoplasms rs4779584 5.00E-07 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. NHGRI|-1
NM_001144758 PHLDB1 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs498872 1.00E-08 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_001144758 PHLDB1 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs498872 5.00E-11 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_001144759 PHLDB1 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs498872 1.00E-08 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_001144759 PHLDB1 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs498872 5.00E-11 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_001144822 CD58 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs1335532 1.00E-07 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_001144822 CD58 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs2300747 3.00E-10 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_001144822 CD58 21244703 http://www.ncbi.nlm.nih.gov/pubmed/21244703 Multiple Sclerosis rs12025416 1.00E-07 Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data. NHGRI|-1
NM_001144823 DENND4A 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs6494537 3.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001144827 RPUSD4 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs563519 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_001144881 PRICKLE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6582406 1.21E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001144881 PRICKLE1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7964774 8.92E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001144881 PRICKLE1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12427230 9.89E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001144881 PRICKLE1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4590936 7.68E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001144882 PRICKLE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6582406 1.21E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001144882 PRICKLE1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7964774 8.92E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001144882 PRICKLE1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12427230 9.89E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001144882 PRICKLE1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4590936 7.68E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001144883 PRICKLE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6582406 1.21E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001144883 PRICKLE1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7964774 8.92E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001144883 PRICKLE1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12427230 9.89E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001144883 PRICKLE1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4590936 7.68E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001144891 MBIP 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs1168987 5.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001144891 MBIP 19198613 http://www.ncbi.nlm.nih.gov/pubmed/19198613 Thyroid Neoplasms rs944289 2.00E-09 Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. NHGRI|-1
NM_001144892 FGF1 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs152528 8.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001144913 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11200014 9.14E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144913 FGFR2 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs2981579 2.00E-10 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_001144913 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2981579 4.36E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144913 FGFR2 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2981579 4.00E-31 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001144913 FGFR2 21060860 http://www.ncbi.nlm.nih.gov/pubmed/21060860 Breast Neoplasms rs2981575 1.00E-08 Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. NHGRI|-1
NM_001144913 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1219648 1.34E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144913 FGFR2 17529973 http://www.ncbi.nlm.nih.gov/pubmed/17529973 Breast Neoplasms rs1219648 1.00E-10 A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. NHGRI|-1
NM_001144913 FGFR2 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs1219648 1.00E-30 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_001144913 FGFR2 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs1219648 2.00E-13 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_001144913 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2420946 1.74E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144913 FGFR2 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs2981582 2.00E-76 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_001144913 FGFR2 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs2901286 4.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001144913 FGFR2 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs10788160 5.00E-15 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001144914 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11200014 9.14E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144914 FGFR2 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs2981579 2.00E-10 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_001144914 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2981579 4.36E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144914 FGFR2 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2981579 4.00E-31 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001144914 FGFR2 21060860 http://www.ncbi.nlm.nih.gov/pubmed/21060860 Breast Neoplasms rs2981575 1.00E-08 Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. NHGRI|-1
NM_001144914 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1219648 1.34E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144914 FGFR2 17529973 http://www.ncbi.nlm.nih.gov/pubmed/17529973 Breast Neoplasms rs1219648 1.00E-10 A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. NHGRI|-1
NM_001144914 FGFR2 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs1219648 1.00E-30 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_001144914 FGFR2 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs1219648 2.00E-13 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_001144914 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2420946 1.74E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144914 FGFR2 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs2981582 2.00E-76 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_001144914 FGFR2 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs2901286 4.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001144914 FGFR2 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs10788160 5.00E-15 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001144915 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11200014 9.14E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144915 FGFR2 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs2981579 2.00E-10 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_001144915 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2981579 4.36E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144915 FGFR2 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2981579 4.00E-31 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001144915 FGFR2 21060860 http://www.ncbi.nlm.nih.gov/pubmed/21060860 Breast Neoplasms rs2981575 1.00E-08 Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. NHGRI|-1
NM_001144915 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1219648 1.34E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144915 FGFR2 17529973 http://www.ncbi.nlm.nih.gov/pubmed/17529973 Breast Neoplasms rs1219648 1.00E-10 A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. NHGRI|-1
NM_001144915 FGFR2 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs1219648 1.00E-30 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_001144915 FGFR2 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs1219648 2.00E-13 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_001144915 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2420946 1.74E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144915 FGFR2 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs2981582 2.00E-76 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_001144915 FGFR2 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs2901286 4.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001144915 FGFR2 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs10788160 5.00E-15 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001144916 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11200014 9.14E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144916 FGFR2 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs2981579 2.00E-10 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_001144916 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2981579 4.36E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144916 FGFR2 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2981579 4.00E-31 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001144916 FGFR2 21060860 http://www.ncbi.nlm.nih.gov/pubmed/21060860 Breast Neoplasms rs2981575 1.00E-08 Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. NHGRI|-1
NM_001144916 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1219648 1.34E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144916 FGFR2 17529973 http://www.ncbi.nlm.nih.gov/pubmed/17529973 Breast Neoplasms rs1219648 1.00E-10 A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. NHGRI|-1
NM_001144916 FGFR2 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs1219648 1.00E-30 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_001144916 FGFR2 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs1219648 2.00E-13 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_001144916 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2420946 1.74E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144916 FGFR2 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs2981582 2.00E-76 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_001144916 FGFR2 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs2901286 4.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001144916 FGFR2 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs10788160 5.00E-15 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001144917 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11200014 9.14E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144917 FGFR2 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs2981579 2.00E-10 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_001144917 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2981579 4.36E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144917 FGFR2 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2981579 4.00E-31 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001144917 FGFR2 21060860 http://www.ncbi.nlm.nih.gov/pubmed/21060860 Breast Neoplasms rs2981575 1.00E-08 Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. NHGRI|-1
NM_001144917 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1219648 1.34E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144917 FGFR2 17529973 http://www.ncbi.nlm.nih.gov/pubmed/17529973 Breast Neoplasms rs1219648 1.00E-10 A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. NHGRI|-1
NM_001144917 FGFR2 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs1219648 1.00E-30 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_001144917 FGFR2 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs1219648 2.00E-13 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_001144917 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2420946 1.74E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144917 FGFR2 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs2981582 2.00E-76 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_001144917 FGFR2 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs2901286 4.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001144917 FGFR2 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs10788160 5.00E-15 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001144918 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11200014 9.14E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144918 FGFR2 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs2981579 2.00E-10 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_001144918 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2981579 4.36E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144918 FGFR2 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2981579 4.00E-31 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001144918 FGFR2 21060860 http://www.ncbi.nlm.nih.gov/pubmed/21060860 Breast Neoplasms rs2981575 1.00E-08 Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. NHGRI|-1
NM_001144918 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1219648 1.34E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144918 FGFR2 17529973 http://www.ncbi.nlm.nih.gov/pubmed/17529973 Breast Neoplasms rs1219648 1.00E-10 A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. NHGRI|-1
NM_001144918 FGFR2 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs1219648 1.00E-30 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_001144918 FGFR2 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs1219648 2.00E-13 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_001144918 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2420946 1.74E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144918 FGFR2 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs2981582 2.00E-76 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_001144918 FGFR2 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs2901286 4.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001144918 FGFR2 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs10788160 5.00E-15 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001144919 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11200014 9.14E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144919 FGFR2 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs2981579 2.00E-10 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_001144919 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2981579 4.36E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144919 FGFR2 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2981579 4.00E-31 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001144919 FGFR2 21060860 http://www.ncbi.nlm.nih.gov/pubmed/21060860 Breast Neoplasms rs2981575 1.00E-08 Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. NHGRI|-1
NM_001144919 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1219648 1.34E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144919 FGFR2 17529973 http://www.ncbi.nlm.nih.gov/pubmed/17529973 Breast Neoplasms rs1219648 1.00E-10 A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. NHGRI|-1
NM_001144919 FGFR2 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs1219648 1.00E-30 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_001144919 FGFR2 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs1219648 2.00E-13 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_001144919 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2420946 1.74E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144919 FGFR2 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs2981582 2.00E-76 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_001144919 FGFR2 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs2901286 4.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001144919 FGFR2 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs10788160 5.00E-15 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001144934 FGF1 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs152528 8.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001144935 FGF1 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs152528 8.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001144952 SDK2 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs3816995 2.00E-07 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_001144958 EFCAB4B 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs887304 8.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001144958 EFCAB4B 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs242033 3.73E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001144958 EFCAB4B 19478329 http://www.ncbi.nlm.nih.gov/pubmed/19478329 "Infertility, Male" rs10848911 4.00E-06 Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. NHGRI|-1
NM_001144959 EFCAB4B 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs887304 8.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001144959 EFCAB4B 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs242033 3.73E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001144959 EFCAB4B 19478329 http://www.ncbi.nlm.nih.gov/pubmed/19478329 "Infertility, Male" rs10848911 4.00E-06 Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. NHGRI|-1
NM_001144961 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071593 4.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144961 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2523503 5.59E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144961 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2523500 2.64E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144961 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2255798 8.43E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144961 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2230365 2.52E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144962 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071593 4.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144962 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2523503 5.59E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144962 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2523500 2.64E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144962 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2255798 8.43E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144962 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2230365 2.52E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144963 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071593 4.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144963 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2523503 5.59E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144963 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2523500 2.64E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144963 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2255798 8.43E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144963 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2230365 2.52E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001144964 NEDD4L 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs17064520 3.22E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001144964 NEDD4L 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs8099014 6.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001144965 NEDD4L 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs17064520 3.22E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001144965 NEDD4L 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs8099014 6.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001144966 NEDD4L 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs17064520 3.22E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001144966 NEDD4L 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs8099014 6.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001144967 NEDD4L 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs17064520 3.22E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001144967 NEDD4L 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs8099014 6.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001144968 NEDD4L 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs17064520 3.22E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001144968 NEDD4L 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs8099014 6.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001144969 NEDD4L 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs17064520 3.22E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001144969 NEDD4L 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs8099014 6.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001144970 NEDD4L 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs17064520 3.22E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001144970 NEDD4L 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs8099014 6.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001144971 NEDD4L 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs17064520 3.22E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001144971 NEDD4L 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs8099014 6.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001144972 SNX20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9302752 1.45E-12 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001144972 SNX20 20018961 http://www.ncbi.nlm.nih.gov/pubmed/20018961 Leprosy rs9302752 4.00E-40 Genomewide association study of leprosy. NHGRI|-1
NM_001144972 SNX20 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs7194886 1.41E-07 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001144972 SNX20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs7194886 2.42E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001144978 MTHFD2L 21738479 http://www.ncbi.nlm.nih.gov/pubmed/21738479 Leukocyte Count rs1371799 2.00E-17 "Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT)." NHGRI|-1
NM_001144990 KIAA1239 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs12505080 7.99E-06 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001144990 KIAA1239 20802204 http://www.ncbi.nlm.nih.gov/pubmed/20802204 Multiple Sclerosis rs13117816 7.00E-06 Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. NHGRI|-1
NM_001145006 MUC7 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs1109501 5.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_001145007 MUC7 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs1109501 5.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_001145014 RFPL4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1423071 4.65E-06 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001145025 EDEM2 20802025 http://www.ncbi.nlm.nih.gov/pubmed/20802025 Protein C rs6120849 7.00E-37 Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. NHGRI|-1
NM_001145044 SLCO3A1 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs3924426 2.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001145044 SLCO3A1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs7495052 3.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001145047 GPN1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs3749147 1.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001145048 GPN1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs3749147 1.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001145049 GPN1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs3749147 1.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001145065 FAM190A 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs41519045 1.48E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001145065 FAM190A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7697633 9.31E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001145065 FAM190A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs12233759 8.45E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001145078 ZNF805 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs2014572 7.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001145079 COG6 18369459 http://www.ncbi.nlm.nih.gov/pubmed/18369459 Psoriasis rs7993214 2.00E-06 A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. NHGRI|-1
NM_001145079 COG6 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs9548988 3.00E-07 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_001145079 COG6 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Alanine Transaminase rs10492681 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001145079 COG6 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs941823 4.00E-12 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001145079 COG6 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs2755237 1.00E-08 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_001145079 COG6 20485516 http://www.ncbi.nlm.nih.gov/pubmed/20485516 Cornea rs2721051 5.00E-10 Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. NHGRI|-1
NM_001145095 HHLA1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Taste rs2014357 9.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001145099 SLC2A6 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2073935 6.05E-08 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001145102 SMAD3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs17293632 3.00E-19 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001145102 SMAD3 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs744910 4.00E-09 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_001145102 SMAD3 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs17228212 2.00E-07 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_001145103 SMAD3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs17293632 3.00E-19 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001145103 SMAD3 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs744910 4.00E-09 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_001145103 SMAD3 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs17228212 2.00E-07 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_001145104 SMAD3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs17293632 3.00E-19 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001145104 SMAD3 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs744910 4.00E-09 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_001145104 SMAD3 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs17228212 2.00E-07 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_001145122 CAPN14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10192210 3.52E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001145128 AKD1 19684573 http://www.ncbi.nlm.nih.gov/pubmed/19684573 Hepatitis C rs9400317 7.00E-06 Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance. NHGRI|-1
NM_001145134 CPT1B 18820697 http://www.ncbi.nlm.nih.gov/pubmed/18820697 Narcolepsy rs5770917 6.00E-08 Variant between CPT1B and CHKB associated with susceptibility to narcolepsy. NHGRI|-1
NM_001145135 CPT1B 18820697 http://www.ncbi.nlm.nih.gov/pubmed/18820697 Narcolepsy rs5770917 6.00E-08 Variant between CPT1B and CHKB associated with susceptibility to narcolepsy. NHGRI|-1
NM_001145136 CPT1B 18820697 http://www.ncbi.nlm.nih.gov/pubmed/18820697 Narcolepsy rs5770917 6.00E-08 Variant between CPT1B and CHKB associated with susceptibility to narcolepsy. NHGRI|-1
NM_001145137 CPT1B 18820697 http://www.ncbi.nlm.nih.gov/pubmed/18820697 Narcolepsy rs5770917 6.00E-08 Variant between CPT1B and CHKB associated with susceptibility to narcolepsy. NHGRI|-1
NM_001145144 SLC1A5 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs11668878 4.00E-07 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_001145145 SLC1A5 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs11668878 4.00E-07 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_001145146 CRHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1635291 2.27E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001145146 CRHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7215239 3.43E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001145146 CRHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1724425 7.77E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001145146 CRHR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs9303521 1.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001145146 CRHR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs9303521 4.00E-06 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001145147 CRHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1635291 2.27E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001145147 CRHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7215239 3.43E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001145147 CRHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1724425 7.77E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001145147 CRHR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs9303521 1.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001145147 CRHR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs9303521 4.00E-06 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001145148 CRHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1635291 2.27E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001145148 CRHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7215239 3.43E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001145148 CRHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1724425 7.77E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001145148 CRHR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs9303521 1.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001145148 CRHR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs9303521 4.00E-06 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001145152 VPS37A 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs3793427 2.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001145154 DNAH14 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2662928 8.79E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001145154 DNAH14 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs1892121 6.78E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001145155 NR2F2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs2567426 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001145155 NR2F2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Hypertension rs2398162 6.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001145156 NR2F2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs2567426 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001145156 NR2F2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Hypertension rs2398162 6.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001145157 NR2F2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs2567426 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001145157 NR2F2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Hypertension rs2398162 6.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001145158 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs7775698 1.00E-14 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001145158 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs7775698 1.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001145158 HBS1L 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-56 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001145158 HBS1L 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-66 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001145158 HBS1L 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 5.00E-13 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001145158 HBS1L 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 8.00E-18 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001145158 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7776054 7.00E-69 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001145158 HBS1L 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs9399137 3.00E-36 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_001145158 HBS1L 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Platelet Count rs9399137 1.00E-09 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001145158 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9373124 7.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001145158 HBS1L 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs9373124 1.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001145158 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4895441 7.00E-86 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001145158 HBS1L 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs4895441 2.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001145158 HBS1L 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs9376092 2.00E-11 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_001145158 HBS1L 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9402686 7.00E-42 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001145158 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs9494145 3.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001145158 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Count rs9483788 1.00E-47 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001145158 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs9483788 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001145158 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 1.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001145158 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 3.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001145158 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 6.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001145161 UBE2QL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs563624 6.12E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001145166 PRMT3 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs7128311 5.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001145167 PRMT3 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs7128311 5.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001145195 SLC39A12 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17661538 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001145195 SLC39A12 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4748442 9.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001145204 SHISA9 18677311 http://www.ncbi.nlm.nih.gov/pubmed/18677311 Schizophrenia rs7192086 6.00E-06 Identification of loci associated with schizophrenia by genome-wide association and follow-up. NHGRI|-1
NM_001145204 SHISA9 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs153091 2.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001145204 SHISA9 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs10521095 2.34E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001145204 SHISA9 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs2113334 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001145205 SHISA9 18677311 http://www.ncbi.nlm.nih.gov/pubmed/18677311 Schizophrenia rs7192086 6.00E-06 Identification of loci associated with schizophrenia by genome-wide association and follow-up. NHGRI|-1
NM_001145205 SHISA9 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs153091 2.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001145205 SHISA9 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs10521095 2.34E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001145205 SHISA9 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs2113334 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001145207 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs7775698 1.00E-14 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001145207 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs7775698 1.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001145207 HBS1L 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-56 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001145207 HBS1L 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-66 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001145207 HBS1L 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 5.00E-13 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001145207 HBS1L 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 8.00E-18 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001145207 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7776054 7.00E-69 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001145207 HBS1L 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs9399137 3.00E-36 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_001145207 HBS1L 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Platelet Count rs9399137 1.00E-09 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001145207 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9373124 7.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001145207 HBS1L 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs9373124 1.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001145207 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4895441 7.00E-86 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001145207 HBS1L 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs4895441 2.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001145207 HBS1L 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs9376092 2.00E-11 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_001145207 HBS1L 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9402686 7.00E-42 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001145207 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs9494145 3.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001145207 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Count rs9483788 1.00E-47 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001145207 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs9483788 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001145207 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 1.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001145207 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 3.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001145207 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 6.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001145211 SLCO2B1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2712800 1.72E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001145212 SLCO2B1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2712800 1.72E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001145279 OPRM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs675026 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001145279 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4598087 1.11E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145279 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754521 9.74E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145279 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2186140 5.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145279 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10499276 8.08E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001145280 OPRM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs675026 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001145280 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4598087 1.11E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145280 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754521 9.74E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145280 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2186140 5.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145280 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10499276 8.08E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001145281 OPRM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs675026 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001145281 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4598087 1.11E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145281 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754521 9.74E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145281 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2186140 5.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145281 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10499276 8.08E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001145282 OPRM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs675026 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001145282 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4598087 1.11E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145282 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754521 9.74E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145282 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2186140 5.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145282 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10499276 8.08E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001145283 OPRM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs675026 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001145283 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4598087 1.11E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145283 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754521 9.74E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145283 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2186140 5.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145283 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10499276 8.08E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001145284 OPRM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs675026 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001145284 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4598087 1.11E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145284 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754521 9.74E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145284 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2186140 5.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145284 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10499276 8.08E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001145285 OPRM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs675026 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001145285 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4598087 1.11E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145285 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754521 9.74E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145285 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2186140 5.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145285 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10499276 8.08E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001145286 OPRM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs675026 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001145286 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4598087 1.11E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145286 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754521 9.74E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145286 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2186140 5.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145286 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10499276 8.08E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001145287 OPRM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs675026 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001145287 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4598087 1.11E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145287 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754521 9.74E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145287 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2186140 5.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001145287 OPRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs10499276 8.08E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001145306 CDK6 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 "Arthritis, Rheumatoid" rs42041 4.00E-06 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_001145306 CDK6 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs2040494 4.00E-07 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001145306 CDK6 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs2282978 1.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001145306 CDK6 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs2282978 1.00E-08 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001145306 CDK6 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs2282978 8.00E-23 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001145306 CDK6 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs445 2.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001145306 CDK6 21738479 http://www.ncbi.nlm.nih.gov/pubmed/21738479 Leukocyte Count rs445 4.00E-07 "Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT)." NHGRI|-1
NM_001145306 CDK6 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs445 7.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001145314 KIAA1712 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs6852435 6.00E-06 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_001145319 PLS1 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs3773506 9.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_001145320 ADAMTSL2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11507716 6.44E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001145335 UBE2Q2 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Cystatin C rs1394125 3.00E-17 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001145353 ELF1 21044949 http://www.ncbi.nlm.nih.gov/pubmed/21044949 "Lupus Erythematosus, Systemic" rs7329174 1.00E-08 ELF1 is associated with systemic lupus erythematosus in Asian populations. NHGRI|-1
NM_001145354 MKLN1 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs10265216 3.00E-06 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_001145354 MKLN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6963574 3.99E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001145357 SIN3A 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs8028182 3.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001145358 SIN3A 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs8028182 3.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001145365 ZNF652 21602798 http://www.ncbi.nlm.nih.gov/pubmed/21602798 Prostatic Neoplasms rs7210100 3.00E-13 Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21. NHGRI|-1
NM_001145365 ZNF652 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs16948048 5.00E-09 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_001145365 ZNF652 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs16948058 2.37E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001145368 PTPN3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4978813 7.01E-06 NBL-GWAS version 1 dbGaP|2845
NM_001145369 PTPN3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4978813 7.01E-06 NBL-GWAS version 1 dbGaP|2845
NM_001145370 PTPN3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4978813 7.01E-06 NBL-GWAS version 1 dbGaP|2845
NM_001145371 PTPN3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4978813 7.01E-06 NBL-GWAS version 1 dbGaP|2845
NM_001145372 PTPN3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4978813 7.01E-06 NBL-GWAS version 1 dbGaP|2845
NM_001145373 OTUD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10734046 6.23E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001145373 OTUD1 18723019 http://www.ncbi.nlm.nih.gov/pubmed/18723019 Crohn Disease rs1398024 4.00E-06 Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2. NHGRI|-1
NM_001145392 TSEN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs9833097 6.72E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001145393 TSEN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs9833097 6.72E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001145394 TSEN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs9833097 6.72E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001145395 TSEN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs9833097 6.72E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001145399 MPPED2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2593549 9.26E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001145399 MPPED2 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs3925584 5.00E-16 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001145414 CHM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs242849 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001145418 TTC28 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs5762430 7.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001145427 SNX18 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4865879 6.81E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001145427 SNX18 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10940434 3.27E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001145432 C4orf52 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs10517086 5.00E-10 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001145432 C4orf52 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs874040 1.00E-16 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001145440 TYW1B 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6460033 1.16E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001145440 TYW1B 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6460033 2.84E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001145440 TYW1B 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs6460033 1.72E-07 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001145443 PFKFB3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2185691 9.67E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001145450 MORN2 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs3099950 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001145466 NCR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844480 4.62E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001145466 NCR3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2857595 1.40E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001145466 NCR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2857595 6.48E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001145466 NCR3 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs2844479 2.00E-08 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001145467 NCR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844480 4.62E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001145467 NCR3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2857595 1.40E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001145467 NCR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2857595 6.48E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001145467 NCR3 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs2844479 2.00E-08 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001145511 NFIA 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs6691768 1.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001145511 NFIA 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9436640 5.00E-18 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001145511 NFIA 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs2989476 3.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_001145511 NFIA 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs472913 2.00E-07 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001145512 NFIA 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs6691768 1.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001145512 NFIA 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9436640 5.00E-18 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001145512 NFIA 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs2989476 3.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_001145512 NFIA 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs472913 2.00E-07 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001145520 RAI14 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10075914 7.33E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001145520 RAI14 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs409045 8.00E-07 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NM_001145521 RAI14 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10075914 7.33E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001145521 RAI14 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs409045 8.00E-07 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NM_001145522 RAI14 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10075914 7.33E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001145522 RAI14 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs409045 8.00E-07 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NM_001145523 RAI14 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10075914 7.33E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001145523 RAI14 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs409045 8.00E-07 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NM_001145525 RAI14 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10075914 7.33E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001145525 RAI14 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs409045 8.00E-07 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NM_001145527 EHMT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10780192 4.80E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001145547 RBM17 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs12251307 1.00E-13 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001145547 RBM17 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs12251307 2.00E-06 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_001145548 ZDHHC7 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs2326458 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001145645 TNFSF13B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4772972 7.05E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001145648 RASGRF1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs3743195 4.06E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001145648 RASGRF1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs3743200 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001145648 RASGRF1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs3816282 2.16E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001145648 RASGRF1 20835236 http://www.ncbi.nlm.nih.gov/pubmed/20835236 Myopia rs939658 2.00E-09 A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. NHGRI|-1
NM_001145666 GLG1 18463975 http://www.ncbi.nlm.nih.gov/pubmed/18463975 Breast Neoplasms rs10871290 4.00E-07 A pilot genome-wide association study of early-onset breast cancer. NHGRI|-1
NM_001145667 GLG1 18463975 http://www.ncbi.nlm.nih.gov/pubmed/18463975 Breast Neoplasms rs10871290 4.00E-07 A pilot genome-wide association study of early-onset breast cancer. NHGRI|-1
NM_001145678 C5orf36 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs17376456 3.00E-15 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_001145715 KPNA7 20228798 http://www.ncbi.nlm.nih.gov/pubmed/20228798 "Colitis, Ulcerative" rs7809799 9.00E-11 Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). NHGRI|-1
NM_001145725 LYAR 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2920228 2.92E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001145725 LYAR 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2920228 3.32E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001145727 IFLTD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4963910 8.37E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001145728 IFLTD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4963910 8.37E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001145729 IFLTD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4963910 8.37E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001145785 MEF2B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10896 1.65E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001145785 MEF2B 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11669988 6.75E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001145794 ANTXR2 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs4389526 9.00E-08 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_001145794 ANTXR2 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs4333130 9.00E-08 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_001145795 SH2B1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs7498665 3.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001145795 SH2B1 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs7498665 5.00E-11 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_001145795 SH2B1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7498665 1.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001145795 SH2B1 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs7359397 2.00E-20 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001145796 SH2B1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs7498665 3.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001145796 SH2B1 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs7498665 5.00E-11 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_001145796 SH2B1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7498665 1.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001145796 SH2B1 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs7359397 2.00E-20 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001145797 SH2B1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs7498665 3.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001145797 SH2B1 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs7498665 5.00E-11 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_001145797 SH2B1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7498665 1.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001145797 SH2B1 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs7359397 2.00E-20 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001145805 IRGM 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs1000113 3.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001145805 IRGM 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs11747270 3.00E-16 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001145805 IRGM 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs7714584 8.00E-19 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001145805 IRGM 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs13361189 2.00E-10 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_001145808 ITGAM 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs9888739 1.00E-15 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_001145808 ITGAM 18204446 http://www.ncbi.nlm.nih.gov/pubmed/18204446 "Lupus Erythematosus, Systemic" rs9888739 2.00E-23 "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci." NHGRI|-1
NM_001145808 ITGAM 19165918 http://www.ncbi.nlm.nih.gov/pubmed/19165918 "Lupus Erythematosus, Systemic" rs11150610 2.00E-06 Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. NHGRI|-1
NM_001145811 SOX6 19714249 http://www.ncbi.nlm.nih.gov/pubmed/19714249 Obesity rs297325 4.00E-07 Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males. NHGRI|-1
NM_001145811 SOX6 19714249 http://www.ncbi.nlm.nih.gov/pubmed/19714249 Obesity rs4756846 5.00E-07 Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males. NHGRI|-1
NM_001145811 SOX6 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7117858 6.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001145811 SOX6 21104366 http://www.ncbi.nlm.nih.gov/pubmed/21104366 Bone Density rs11023787 5.00E-16 A genome-wide association analysis implicates SOX6 as a candidate gene for wrist bone mass. NHGRI|-1
NM_001145812 SH2B1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs7498665 3.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001145812 SH2B1 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs7498665 5.00E-11 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_001145812 SH2B1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7498665 1.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001145812 SH2B1 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs7359397 2.00E-20 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001145816 HPGD 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs6852435 6.00E-06 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_001145819 SOX6 19714249 http://www.ncbi.nlm.nih.gov/pubmed/19714249 Obesity rs297325 4.00E-07 Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males. NHGRI|-1
NM_001145819 SOX6 19714249 http://www.ncbi.nlm.nih.gov/pubmed/19714249 Obesity rs4756846 5.00E-07 Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males. NHGRI|-1
NM_001145819 SOX6 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7117858 6.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001145819 SOX6 21104366 http://www.ncbi.nlm.nih.gov/pubmed/21104366 Bone Density rs11023787 5.00E-16 A genome-wide association analysis implicates SOX6 as a candidate gene for wrist bone mass. NHGRI|-1
NM_001145853 WFS1 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs4689388 1.00E-08 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001145853 WFS1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs1801214 3.00E-08 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001145903 C2 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs9332739 2.00E-23 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1042663 2.97E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1042663 3.14E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001145903 C2 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs9380272 2.00E-08 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs550605 4.38E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs550605 4.98E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs638383 4.76E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs497239 6.02E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs497239 7.82E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs547154 2.70E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs547154 2.90E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001145903 C2 21105107 http://www.ncbi.nlm.nih.gov/pubmed/21105107 "Carcinoma, Hepatocellular" rs9267673 2.00E-06 Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma. NHGRI|-1
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9267673 2.30E-33 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001145903 C2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs644045 2.06E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs511294 1.45E-13 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs511294 6.27E-13 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs544167 2.48E-13 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001145903 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs544167 7.79E-13 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001145909 TANC1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs13022357 1.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001145933 TKTL1 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs766420 9.00E-09 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_001145934 TKTL1 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs766420 9.00E-09 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_001145944 SLCO1C1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs10770705 8.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001145945 SLCO1C1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs10770705 8.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001145946 SLCO1C1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs10770705 8.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001145966 MKI67 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Vitamin K 1 rs2387326 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001145966 MKI67 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1314589 3.95E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001145966 MKI67 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1314589 8.76E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001145966 MKI67 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs11818629 3.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001145966 MKI67 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs541392 6.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001146 ANGPT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7818981 9.90E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001146 ANGPT1 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs4534106 1.00E-06 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001146 ANGPT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4734938 8.67E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001146008 SLCO5A1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs16936455 7.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001146008 SLCO5A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6472491 3.15E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001146009 SLCO5A1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs16936455 7.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001146009 SLCO5A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6472491 3.15E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001146054 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs3857059 3.60E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146054 SNCA 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs2736990 2.00E-16 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_001146054 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2736990 5.69E-09 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146054 SNCA 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs2736990 7.00E-08 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_001146054 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356188 8.41E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001146054 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs3775439 4.43E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146054 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs894278 2.64E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146054 SNCA 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs6532197 1.00E-07 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_001146054 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4106153 9.18E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001146054 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1504489 8.42E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001146054 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12644119 2.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146054 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356229 5.48E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001146054 SNCA 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs356219 2.00E-47 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001146054 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11931074 4.78E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146054 SNCA 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson Disease rs11931074 7.00E-17 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_001146054 SNCA 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs356220 2.00E-19 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_001146054 SNCA 20711177 http://www.ncbi.nlm.nih.gov/pubmed/20711177 Parkinson Disease rs356220 3.00E-11 Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. NHGRI|-1
NM_001146054 SNCA 21084426 http://www.ncbi.nlm.nih.gov/pubmed/21084426 Parkinson Disease rs356220 3.00E-08 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. NHGRI|-1
NM_001146054 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356220 6.99E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146054 SNCA 21044948 http://www.ncbi.nlm.nih.gov/pubmed/21044948 Parkinson Disease rs356220 9.00E-16 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. NHGRI|-1
NM_001146055 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs3857059 3.60E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146055 SNCA 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs2736990 2.00E-16 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_001146055 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2736990 5.69E-09 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146055 SNCA 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs2736990 7.00E-08 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_001146055 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356188 8.41E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001146055 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs3775439 4.43E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146055 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs894278 2.64E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146055 SNCA 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs6532197 1.00E-07 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_001146055 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4106153 9.18E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001146055 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1504489 8.42E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001146055 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12644119 2.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146055 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356229 5.48E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001146055 SNCA 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs356219 2.00E-47 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001146055 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11931074 4.78E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146055 SNCA 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson Disease rs11931074 7.00E-17 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_001146055 SNCA 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs356220 2.00E-19 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_001146055 SNCA 20711177 http://www.ncbi.nlm.nih.gov/pubmed/20711177 Parkinson Disease rs356220 3.00E-11 Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. NHGRI|-1
NM_001146055 SNCA 21084426 http://www.ncbi.nlm.nih.gov/pubmed/21084426 Parkinson Disease rs356220 3.00E-08 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. NHGRI|-1
NM_001146055 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356220 6.99E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001146055 SNCA 21044948 http://www.ncbi.nlm.nih.gov/pubmed/21044948 Parkinson Disease rs356220 9.00E-16 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. NHGRI|-1
NM_001146075 RPAP3 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs11610206 3.00E-07 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001146076 RPAP3 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs11610206 3.00E-07 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001146077 CLDN14 19561606 http://www.ncbi.nlm.nih.gov/pubmed/19561606 Kidney Calculi rs219780 4.00E-12 Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density. NHGRI|-1
NM_001146078 CLDN14 19561606 http://www.ncbi.nlm.nih.gov/pubmed/19561606 Kidney Calculi rs219780 4.00E-12 Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density. NHGRI|-1
NM_001146079 CLDN14 19561606 http://www.ncbi.nlm.nih.gov/pubmed/19561606 Kidney Calculi rs219780 4.00E-12 Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density. NHGRI|-1
NM_001146188 TOX3 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs3803662 1.00E-36 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_001146188 TOX3 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs3803662 1.00E-09 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_001146188 TOX3 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs3803662 3.00E-15 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001146188 TOX3 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs3803662 4.00E-07 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_001146188 TOX3 17529974 http://www.ncbi.nlm.nih.gov/pubmed/17529974 Breast Neoplasms rs3803662 6.00E-19 Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer. NHGRI|-1
NM_001146188 TOX3 20585626 http://www.ncbi.nlm.nih.gov/pubmed/20585626 Breast Neoplasms rs4784227 1.00E-28 Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium. NHGRI|-1
NM_001146188 TOX3 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs3112612 4.00E-10 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_001146188 TOX3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3104807 1.01E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001146188 TOX3 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Exploratory Behavior rs4131099 4.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_001146188 TOX3 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1362756 5.00E-09 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_001146189 ZNF407 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7245160 4.22E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001146190 ZNF407 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7245160 4.22E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001146191 MPZL1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs12757250 9.23E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001146202 RASGRP4 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs892055 5.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_001146203 RASGRP4 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs892055 5.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_001146204 RASGRP4 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs892055 5.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_001146206 RASGRP4 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs892055 5.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_001146207 RASGRP4 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs892055 5.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_001146209 PDE2A 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs12418204 5.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_001146209 PDE2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs341076 4.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001146209 PDE2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs193170 3.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001146213 TBC1D15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs328764 7.52E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001146214 TBC1D15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs328764 7.52E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001146216 TACC1 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs7832232 5.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_001146265 GPR85 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 acylcarnitine rs10953730 2.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_001146265 GPR85 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10229603 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001146266 GPR85 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 acylcarnitine rs10953730 2.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_001146266 GPR85 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10229603 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001146267 GPR85 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 acylcarnitine rs10953730 2.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_001146267 GPR85 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10229603 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001146274 TCF7L2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7901695 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001146274 TCF7L2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs7901695 1.00E-48 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001146274 TCF7L2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs4506565 5.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001146274 TCF7L2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4506565 1.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001146274 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.25E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001146274 TCF7L2 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs7903146 1.00E-30 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001146274 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001146274 TCF7L2 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs7903146 2.00E-10 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001146274 TCF7L2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs7903146 2.00E-31 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001146274 TCF7L2 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs7903146 2.00E-34 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001146274 TCF7L2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7903146 2.00E-51 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001146274 TCF7L2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7903146 3.00E-23 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001146274 TCF7L2 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs7903146 5.00E-08 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_001146274 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 6.00E-16 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001146274 TCF7L2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs7903146 7.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001146274 TCF7L2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs7903146 8.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001146274 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 9.00E-30 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001146274 TCF7L2 20849430 http://www.ncbi.nlm.nih.gov/pubmed/20849430 "Hemoglobin A, Glycosylated" rs7903146 1.00E-07 The TCF7L2 diabetes risk variant is associated with HbAG??(C) levels: a genome-wide association meta-analysis. NHGRI|-1
NM_001146274 TCF7L2 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs12243326 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001146274 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12255372 1.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001146283 TCF7L2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7901695 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001146283 TCF7L2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs7901695 1.00E-48 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001146283 TCF7L2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs4506565 5.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001146283 TCF7L2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4506565 1.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001146283 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.25E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001146283 TCF7L2 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs7903146 1.00E-30 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001146283 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001146283 TCF7L2 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs7903146 2.00E-10 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001146283 TCF7L2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs7903146 2.00E-31 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001146283 TCF7L2 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs7903146 2.00E-34 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001146283 TCF7L2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7903146 2.00E-51 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001146283 TCF7L2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7903146 3.00E-23 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001146283 TCF7L2 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs7903146 5.00E-08 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_001146283 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 6.00E-16 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001146283 TCF7L2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs7903146 7.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001146283 TCF7L2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs7903146 8.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001146283 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 9.00E-30 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001146283 TCF7L2 20849430 http://www.ncbi.nlm.nih.gov/pubmed/20849430 "Hemoglobin A, Glycosylated" rs7903146 1.00E-07 The TCF7L2 diabetes risk variant is associated with HbAG??(C) levels: a genome-wide association meta-analysis. NHGRI|-1
NM_001146283 TCF7L2 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs12243326 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001146283 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12255372 1.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001146284 TCF7L2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7901695 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001146284 TCF7L2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs7901695 1.00E-48 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001146284 TCF7L2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs4506565 5.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001146284 TCF7L2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4506565 1.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001146284 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.25E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001146284 TCF7L2 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs7903146 1.00E-30 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001146284 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001146284 TCF7L2 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs7903146 2.00E-10 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001146284 TCF7L2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs7903146 2.00E-31 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001146284 TCF7L2 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs7903146 2.00E-34 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001146284 TCF7L2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7903146 2.00E-51 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001146284 TCF7L2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7903146 3.00E-23 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001146284 TCF7L2 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs7903146 5.00E-08 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_001146284 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 6.00E-16 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001146284 TCF7L2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs7903146 7.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001146284 TCF7L2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs7903146 8.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001146284 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 9.00E-30 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001146284 TCF7L2 20849430 http://www.ncbi.nlm.nih.gov/pubmed/20849430 "Hemoglobin A, Glycosylated" rs7903146 1.00E-07 The TCF7L2 diabetes risk variant is associated with HbAG??(C) levels: a genome-wide association meta-analysis. NHGRI|-1
NM_001146284 TCF7L2 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs12243326 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001146284 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12255372 1.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001146285 TCF7L2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7901695 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001146285 TCF7L2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs7901695 1.00E-48 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001146285 TCF7L2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs4506565 5.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001146285 TCF7L2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4506565 1.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001146285 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.25E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001146285 TCF7L2 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs7903146 1.00E-30 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001146285 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001146285 TCF7L2 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs7903146 2.00E-10 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001146285 TCF7L2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs7903146 2.00E-31 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001146285 TCF7L2 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs7903146 2.00E-34 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001146285 TCF7L2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7903146 2.00E-51 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001146285 TCF7L2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7903146 3.00E-23 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001146285 TCF7L2 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs7903146 5.00E-08 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_001146285 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 6.00E-16 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001146285 TCF7L2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs7903146 7.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001146285 TCF7L2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs7903146 8.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001146285 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 9.00E-30 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001146285 TCF7L2 20849430 http://www.ncbi.nlm.nih.gov/pubmed/20849430 "Hemoglobin A, Glycosylated" rs7903146 1.00E-07 The TCF7L2 diabetes risk variant is associated with HbAG??(C) levels: a genome-wide association meta-analysis. NHGRI|-1
NM_001146285 TCF7L2 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs12243326 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001146285 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12255372 1.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001146286 TCF7L2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7901695 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001146286 TCF7L2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs7901695 1.00E-48 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001146286 TCF7L2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs4506565 5.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001146286 TCF7L2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4506565 1.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001146286 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.25E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001146286 TCF7L2 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs7903146 1.00E-30 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001146286 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001146286 TCF7L2 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs7903146 2.00E-10 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001146286 TCF7L2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs7903146 2.00E-31 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001146286 TCF7L2 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs7903146 2.00E-34 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001146286 TCF7L2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7903146 2.00E-51 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001146286 TCF7L2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7903146 3.00E-23 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001146286 TCF7L2 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs7903146 5.00E-08 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_001146286 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 6.00E-16 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001146286 TCF7L2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs7903146 7.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001146286 TCF7L2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs7903146 8.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001146286 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 9.00E-30 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001146286 TCF7L2 20849430 http://www.ncbi.nlm.nih.gov/pubmed/20849430 "Hemoglobin A, Glycosylated" rs7903146 1.00E-07 The TCF7L2 diabetes risk variant is associated with HbAG??(C) levels: a genome-wide association meta-analysis. NHGRI|-1
NM_001146286 TCF7L2 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs12243326 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001146286 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12255372 1.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001146312 MYOCD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs8068445 1.10E-05 NBL-GWAS version 2 dbGaP|2895
NM_001146313 MYOCD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs8068445 1.10E-05 NBL-GWAS version 2 dbGaP|2895
NM_001146319 GRAMD3 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs1073203 9.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001146320 GRAMD3 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs1073203 9.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001146321 GRAMD3 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs1073203 9.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001146322 GRAMD3 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs1073203 9.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001146335 SLC6A15 20662065 http://www.ncbi.nlm.nih.gov/pubmed/20662065 Lupus Vulgaris rs2403106 3.00E-06 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. NHGRI|-1
NM_001146335 SLC6A15 21521612 http://www.ncbi.nlm.nih.gov/pubmed/21521612 "Depressive Disorder, Major" rs1545843 1.00E-09 The neuronal transporter gene SLC6A15 confers risk to major depression. NHGRI|-1
NM_001146335 SLC6A15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2125716 1.13E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001146336 TMEM114 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs3112740 6.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001146339 VSTM2B 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs10403021 2.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001146339 VSTM2B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17691420 3.10E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001146339 VSTM2B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8110188 1.03E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001146339 VSTM2B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8110188 6.42E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001146341 ANKRD34C 20835236 http://www.ncbi.nlm.nih.gov/pubmed/20835236 Myopia rs939658 2.00E-09 A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. NHGRI|-1
NM_001146590 AGXT2L1 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs4956211 1.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_001146627 AGXT2L1 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs4956211 1.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_001146694 KDM4C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10815468 4.26E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001146694 KDM4C 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs4742269 5.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_001146695 KDM4C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10815468 4.26E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001146695 KDM4C 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs4742269 5.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_001146696 KDM4C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10815468 4.26E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001146696 KDM4C 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs4742269 5.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_001146698 RBM19 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 C-Reactive Protein rs11066587 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001146699 RBM19 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 C-Reactive Protein rs11066587 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001146726 TIMD4 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs1501908 1.00E-11 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001148 ANK2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4834308 6.98E-06 NBL-GWAS version 1 dbGaP|2845
NM_001149 ANK3 20185149 http://www.ncbi.nlm.nih.gov/pubmed/20185149 Schizophrenia rs10761482 8.00E-06 Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. NHGRI|-1
NM_001149 ANK3 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs10994336 9.00E-09 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001149 ANK3 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs10994338 5.00E-07 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001150 ANPEP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs6496603 1.26E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001151 SLC25A4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6818704 4.66E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001154 ANXA5 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs55645543 5.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001154 ANXA5 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs7659604 9.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001155 ANXA6 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs17728338 1.00E-20 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NM_001158261 CCDC42 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1971773 5.48E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001158261 CCDC42 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6503137 8.24E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001159285 ADAD1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs17388568 9.00E-07 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001159285 ADAD1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs17388568 3.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001159295 ADAD1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs17388568 9.00E-07 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001159295 ADAD1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs17388568 3.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001159531 BEGAIN 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs6575793 1.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001159542 POU5F1B 17401363 http://www.ncbi.nlm.nih.gov/pubmed/17401363 Prostatic Neoplasms rs1447295 2.00E-14 Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. NHGRI|-1
NM_001159542 POU5F1B 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs1447295 2.00E-19 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_001159542 POU5F1B 17401366 http://www.ncbi.nlm.nih.gov/pubmed/17401366 Prostatic Neoplasms rs1447295 6.00E-18 Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. NHGRI|-1
NM_001159542 POU5F1B 18264096 http://www.ncbi.nlm.nih.gov/pubmed/18264096 Prostatic Neoplasms rs4242382 3.00E-19 Multiple loci identified in a genome-wide association study of prostate cancer. NHGRI|-1
NM_001159542 POU5F1B 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs4242384 2.00E-24 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001159542 POU5F1B 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs4242384 3.00E-16 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_001159542 POU5F1B 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs4242384 3.00E-16 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_001159542 POU5F1B 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs7837688 1.00E-25 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_001159542 POU5F1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs6470531 1.63E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001159542 POU5F1B 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs9642880 2.00E-18 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_001159542 POU5F1B 20348956 http://www.ncbi.nlm.nih.gov/pubmed/20348956 Urinary Bladder Neoplasms rs9642880 7.00E-12 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001159542 POU5F1B 18794855 http://www.ncbi.nlm.nih.gov/pubmed/18794855 Urinary Bladder Neoplasms rs9642880 9.00E-12 Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_001159542 POU5F1B 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs1456315 2.00E-29 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_001159542 POU5F1B 17401366 http://www.ncbi.nlm.nih.gov/pubmed/17401366 Prostatic Neoplasms rs16901979 1.00E-12 Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. NHGRI|-1
NM_001159542 POU5F1B 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs16901979 3.00E-14 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_001159542 POU5F1B 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2456449 8.00E-10 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_001159542 POU5F1B 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs16902094 6.00E-15 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_001159542 POU5F1B 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs445114 5.00E-10 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_001159542 POU5F1B 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs445114 5.00E-07 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_001159542 POU5F1B 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs13281615 5.00E-12 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_001159542 POU5F1B 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs1562430 3.00E-11 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_001159542 POU5F1B 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs1562430 6.00E-07 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001159542 POU5F1B 17618283 http://www.ncbi.nlm.nih.gov/pubmed/17618283 Colorectal Neoplasms rs10505477 3.00E-11 Genome-wide association scan identifies a colorectal cancer susceptibility locus on chromosome 8q24. NHGRI|-1
NM_001159542 POU5F1B 21242260 http://www.ncbi.nlm.nih.gov/pubmed/21242260 Colonic Neoplasms rs6983267 2.00E-08 Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population. NHGRI|-1
NM_001159542 POU5F1B 17618284 http://www.ncbi.nlm.nih.gov/pubmed/17618284 Colorectal Neoplasms rs6983267 1.00E-14 A genome-wide association scan of tag SNPs identifies a susceptibility variant for colorectal cancer at 8q24.21. NHGRI|-1
NM_001159542 POU5F1B 18372905 http://www.ncbi.nlm.nih.gov/pubmed/18372905 Colorectal Neoplasms rs6983267 7.00E-11 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. NHGRI|-1
NM_001159542 POU5F1B 18264096 http://www.ncbi.nlm.nih.gov/pubmed/18264096 Prostatic Neoplasms rs6983267 7.00E-12 Multiple loci identified in a genome-wide association study of prostate cancer. NHGRI|-1
NM_001159542 POU5F1B 17401363 http://www.ncbi.nlm.nih.gov/pubmed/17401363 Prostatic Neoplasms rs6983267 9.00E-13 Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. NHGRI|-1
NM_001159542 POU5F1B 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs6983267 9.00E-13 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_001159542 POU5F1B 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs6983267 9.00E-06 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_001159542 POU5F1B 18372901 http://www.ncbi.nlm.nih.gov/pubmed/18372901 Colorectal Neoplasms rs7014346 9.00E-26 Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. NHGRI|-1
NM_001159575 SCNN1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10849446 3.66E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001159575 SCNN1A 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs11064153 5.39E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001159576 SCNN1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10849446 3.66E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001159576 SCNN1A 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs11064153 5.39E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001159597 SH3YL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10181051 5.38E-05 NBL-GWAS version 2 dbGaP|2895
NM_001159597 SH3YL1 21423239 http://www.ncbi.nlm.nih.gov/pubmed/21423239 "Suicide, Attempted" rs300774 5.00E-08 A genome-wide association study of attempted suicide. NHGRI|-1
NM_001159643 MCTP2 19483685 http://www.ncbi.nlm.nih.gov/pubmed/19483685 Drug-Induced Liver Injury rs4984390 4.00E-06 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. NHGRI|-1
NM_001159643 MCTP2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs1014922 3.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001159643 MCTP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2199724 2.59E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001159643 MCTP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2046006 9.03E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001159643 MCTP2 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Alkaline Phosphatase rs7173947 3.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001159643 MCTP2 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs933769 7.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_001159643 MCTP2 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs4321143 7.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001159644 MCTP2 19483685 http://www.ncbi.nlm.nih.gov/pubmed/19483685 Drug-Induced Liver Injury rs4984390 4.00E-06 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. NHGRI|-1
NM_001159644 MCTP2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs1014922 3.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001159644 MCTP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2199724 2.59E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001159644 MCTP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2046006 9.03E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001159644 MCTP2 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Alkaline Phosphatase rs7173947 3.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001159644 MCTP2 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs933769 7.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_001159644 MCTP2 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs4321143 7.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001159651 BOD1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs359457 3.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001159651 BOD1 19165155 http://www.ncbi.nlm.nih.gov/pubmed/19165155 Adiponectin rs7722022 9.00E-06 Genome-wide linkage and association analyses to identify genes influencing adiponectin levels: the GEMS Study. NHGRI|-1
NM_001159651 BOD1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs889014 9.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001159694 EMCN 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Piperazines rs1405687 5.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001159736 BUD13 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs28927680 2.00E-17 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_001159736 BUD13 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs11825181 3.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001159736 BUD13 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs11820589 6.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001159736 BUD13 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs10790162 3.00E-15 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001159736 BUD13 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs10790162 5.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001159736 BUD13 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs10790162 7.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001159736 BUD13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1009746 1.83E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001159736 BUD13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1009746 4.03E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001159736 BUD13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17473320 8.79E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001159736 BUD13 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs490592 1.00E-06 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001159736 BUD13 21160409 http://www.ncbi.nlm.nih.gov/pubmed/21160409 HIV-1 rs1240773 8.00E-06 Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population. NHGRI|-1
NM_001159736 BUD13 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs4938303 4.00E-21 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001159736 BUD13 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Triglycerides rs7350481 1.00E-49 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001159736 BUD13 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs180358 6.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001159736 BUD13 19185284 http://www.ncbi.nlm.nih.gov/pubmed/19185284 alpha-Tocopherol rs12272004 8.00E-10 "Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study." NHGRI|-1
NM_001159736 BUD13 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs12272004 7.00E-07 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001159736 BUD13 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Triglycerides rs12272004 5.00E-13 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001159736 BUD13 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs1558861 2.00E-06 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001159736 BUD13 18193046 http://www.ncbi.nlm.nih.gov/pubmed/18193046 Triglycerides rs1558861 2.00E-26 Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. NHGRI|-1
NM_001159736 BUD13 20838585 http://www.ncbi.nlm.nih.gov/pubmed/20838585 Triglycerides rs12280753 8.00E-06 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. NHGRI|-1
NM_001159740 LTA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2009658 6.64E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001159740 LTA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2229094 1.68E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001159740 LTA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112071469 2.90E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001159770 SLC39A11 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs8066857 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001159920 FLT1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs17086609 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001159944 EVI5L 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs558718 4.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_001159995 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001159995 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_001159995 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001159995 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001159995 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001159995 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001159996 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001159996 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_001159996 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001159996 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001159996 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001159996 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001159999 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001159999 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_001159999 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001159999 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001159999 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001159999 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160001 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001160001 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_001160001 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001160001 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160001 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160001 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160002 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001160002 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_001160002 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001160002 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160002 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160002 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160004 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001160004 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_001160004 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001160004 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160004 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160004 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160005 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001160005 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_001160005 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001160005 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160005 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160005 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160007 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001160007 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_001160007 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001160007 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160007 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160007 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160008 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001160008 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_001160008 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001160008 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160008 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160008 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001160011 ST6GALNAC3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs10873876 4.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001160011 ST6GALNAC3 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Personality rs12753569 8.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_001160030 FLT1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs17086609 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001160031 FLT1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs17086609 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001160100 CLDN10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs870707 2.95E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001160125 KLF6 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs6601764 9.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001160125 KLF6 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs2031577 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001160125 KLF6 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Mass Index rs10458787 1.00E-06 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_001160125 KLF6 20662065 http://www.ncbi.nlm.nih.gov/pubmed/20662065 Lupus Vulgaris rs1391511 7.00E-06 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. NHGRI|-1
NM_001160125 KLF6 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs2764980 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001160125 KLF6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17135017 4.32E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001160125 KLF6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11251836 2.88E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001160125 KLF6 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Bone Density rs2165468 1.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001160125 KLF6 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4881184 5.93E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001160147 DDHD1 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs1380131 9.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_001160148 DDHD1 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs1380131 9.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_001160154 MGAT4A 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs12618769 1.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_001160160 SCN5A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs11129795 5.00E-10 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001160160 SCN5A 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs11129795 5.00E-14 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001160160 SCN5A 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12053903 1.00E-14 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001160160 SCN5A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs12053903 1.00E-07 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001160160 SCN5A 19389651 http://www.ncbi.nlm.nih.gov/pubmed/19389651 Electrocardiography rs7638909 2.00E-06 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. NHGRI|-1
NM_001160160 SCN5A 21347284 http://www.ncbi.nlm.nih.gov/pubmed/21347284 Electrocardiography rs3922844 3.00E-23 Genome-wide association studies of the PR interval in African Americans. NHGRI|-1
NM_001160160 SCN5A 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs11708996 6.00E-26 Genome-wide association study of PR interval. NHGRI|-1
NM_001160160 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11708996 7.00E-06 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001160160 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11710077 1.00E-06 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001160160 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9851724 6.00E-16 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001160161 SCN5A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs11129795 5.00E-10 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001160161 SCN5A 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs11129795 5.00E-14 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001160161 SCN5A 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12053903 1.00E-14 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001160161 SCN5A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs12053903 1.00E-07 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001160161 SCN5A 19389651 http://www.ncbi.nlm.nih.gov/pubmed/19389651 Electrocardiography rs7638909 2.00E-06 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. NHGRI|-1
NM_001160161 SCN5A 21347284 http://www.ncbi.nlm.nih.gov/pubmed/21347284 Electrocardiography rs3922844 3.00E-23 Genome-wide association studies of the PR interval in African Americans. NHGRI|-1
NM_001160161 SCN5A 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs11708996 6.00E-26 Genome-wide association study of PR interval. NHGRI|-1
NM_001160161 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11708996 7.00E-06 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001160161 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11710077 1.00E-06 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001160161 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9851724 6.00E-16 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001160167 PRR5L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2292648 9.25E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001160168 PRR5L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2292648 9.25E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001160169 PRR5L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2292648 9.25E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001160170 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 2.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160170 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 4.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160170 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 8.00E-08 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160171 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 2.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160171 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 4.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160171 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 8.00E-08 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160172 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 2.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160172 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 4.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160172 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 8.00E-08 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160173 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 2.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160173 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 4.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160173 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 8.00E-08 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160174 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 2.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160174 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 4.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160174 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 8.00E-08 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160175 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 2.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160175 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 4.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160175 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 8.00E-08 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160176 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 2.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160176 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 4.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160176 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 8.00E-08 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160179 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 2.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160179 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 4.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160179 NAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 8.00E-08 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_001160226 CNR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs964647 2.09E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001160230 ADARB1 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Respiratory Function Tests rs2838815 3.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_001160233 ATP1A1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7552721 5.96E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001160234 ATP1A1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7552721 5.96E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001160258 CNR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs964647 2.09E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001160259 CNR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs964647 2.09E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001160260 CNR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs964647 2.09E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001160277 CERKL 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs993648 3.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001160301 DPYD 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs11165846 9.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001160367 CDK10 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs258322 2.00E-23 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_001160367 CDK10 19578364 http://www.ncbi.nlm.nih.gov/pubmed/19578364 Melanoma rs258322 3.00E-27 Genome-wide association study identifies three loci associated with melanoma risk. NHGRI|-1
NM_001160408 TULP3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10774085 3.51E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001160417 ZBP1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs2073145 2.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_001160418 ZBP1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs2073145 2.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_001160419 ZBP1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs2073145 2.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_001160423 IGF2BP1 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs9674544 2.00E-08 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001160423 IGF2BP1 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs9674544 8.00E-07 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001160708 POLR3B 21084426 http://www.ncbi.nlm.nih.gov/pubmed/21084426 Parkinson Disease rs4964469 2.00E-07 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. NHGRI|-1
NM_001160708 POLR3B 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs3891355 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_001161352 KCNMA1 21708048 http://www.ncbi.nlm.nih.gov/pubmed/21708048 Obesity rs2116830 3.00E-10 Genome Wide Association Study Identifies KCNMA1 Contributing to Human Obesity. NHGRI|-1
NM_001161352 KCNMA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1247755 7.47E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001161352 KCNMA1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2917454 3.30E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001161352 KCNMA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12219105 9.68E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001161352 KCNMA1 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs4979906 7.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_001161353 KCNMA1 21708048 http://www.ncbi.nlm.nih.gov/pubmed/21708048 Obesity rs2116830 3.00E-10 Genome Wide Association Study Identifies KCNMA1 Contributing to Human Obesity. NHGRI|-1
NM_001161353 KCNMA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1247755 7.47E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001161353 KCNMA1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2917454 3.30E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001161353 KCNMA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12219105 9.68E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001161353 KCNMA1 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs4979906 7.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_001161407 NDFIP2 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs2039553 7.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_001161407 NDFIP2 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs9574565 3.00E-07 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_001161407 NDFIP2 20862305 http://www.ncbi.nlm.nih.gov/pubmed/20862305 "Diabetes Mellitus, Type 2" rs1359790 6.00E-09 Identification of new genetic risk variants for type 2 diabetes. NHGRI|-1
NM_001161429 RANBP3L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4354072 1.61E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001161520 COG5 20112360 http://www.ncbi.nlm.nih.gov/pubmed/20112360 Osteoarthritis rs3815148 8.00E-08 A genome-wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22. NHGRI|-1
NM_001161560 TNIK 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11920719 4.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001161560 TNIK 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs2088885 6.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_001161560 TNIK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs13065441 3.16E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001161561 TNIK 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11920719 4.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001161561 TNIK 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs2088885 6.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_001161561 TNIK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs13065441 3.16E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001161562 TNIK 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11920719 4.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001161562 TNIK 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs2088885 6.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_001161562 TNIK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs13065441 3.16E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001161563 TNIK 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11920719 4.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001161563 TNIK 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs2088885 6.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_001161563 TNIK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs13065441 3.16E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001161564 TNIK 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11920719 4.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001161564 TNIK 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs2088885 6.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_001161564 TNIK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs13065441 3.16E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001161565 TNIK 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11920719 4.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001161565 TNIK 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs2088885 6.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_001161565 TNIK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs13065441 3.16E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001161566 TNIK 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11920719 4.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001161566 TNIK 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs2088885 6.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_001161566 TNIK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs13065441 3.16E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001161576 SAMD4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4901519 7.56E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001161577 SAMD4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4901519 7.56E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001161656 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs7775698 1.00E-14 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161656 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs7775698 1.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161656 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-56 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161656 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-66 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161656 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 5.00E-13 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161656 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 8.00E-18 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161656 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7776054 7.00E-69 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161656 MYB 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs9399137 3.00E-36 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_001161656 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Platelet Count rs9399137 1.00E-09 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161656 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9373124 7.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161656 MYB 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs9373124 1.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001161656 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4895441 7.00E-86 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161656 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs4895441 2.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161656 MYB 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs9376092 2.00E-11 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_001161656 MYB 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9402686 7.00E-42 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001161656 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs9494145 3.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161656 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Count rs9483788 1.00E-47 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161656 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs9483788 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161656 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 1.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161656 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 3.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161656 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 6.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161657 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs7775698 1.00E-14 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161657 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs7775698 1.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161657 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-56 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161657 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-66 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161657 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 5.00E-13 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161657 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 8.00E-18 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161657 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7776054 7.00E-69 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161657 MYB 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs9399137 3.00E-36 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_001161657 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Platelet Count rs9399137 1.00E-09 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161657 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9373124 7.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161657 MYB 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs9373124 1.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001161657 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4895441 7.00E-86 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161657 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs4895441 2.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161657 MYB 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs9376092 2.00E-11 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_001161657 MYB 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9402686 7.00E-42 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001161657 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs9494145 3.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161657 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Count rs9483788 1.00E-47 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161657 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs9483788 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161657 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 1.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161657 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 3.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161657 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 6.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161658 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs7775698 1.00E-14 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161658 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs7775698 1.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161658 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-56 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161658 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-66 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161658 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 5.00E-13 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161658 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 8.00E-18 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161658 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7776054 7.00E-69 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161658 MYB 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs9399137 3.00E-36 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_001161658 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Platelet Count rs9399137 1.00E-09 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161658 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9373124 7.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161658 MYB 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs9373124 1.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001161658 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4895441 7.00E-86 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161658 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs4895441 2.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161658 MYB 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs9376092 2.00E-11 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_001161658 MYB 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9402686 7.00E-42 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001161658 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs9494145 3.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161658 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Count rs9483788 1.00E-47 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161658 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs9483788 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161658 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 1.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161658 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 3.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161658 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 6.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161659 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs7775698 1.00E-14 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161659 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs7775698 1.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161659 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-56 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161659 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-66 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161659 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 5.00E-13 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161659 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 8.00E-18 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161659 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7776054 7.00E-69 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161659 MYB 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs9399137 3.00E-36 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_001161659 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Platelet Count rs9399137 1.00E-09 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161659 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9373124 7.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161659 MYB 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs9373124 1.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001161659 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4895441 7.00E-86 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161659 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs4895441 2.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161659 MYB 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs9376092 2.00E-11 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_001161659 MYB 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9402686 7.00E-42 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001161659 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs9494145 3.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161659 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Count rs9483788 1.00E-47 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161659 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs9483788 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161659 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 1.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161659 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 3.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161659 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 6.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161660 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs7775698 1.00E-14 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161660 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs7775698 1.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161660 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-56 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161660 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-66 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161660 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 5.00E-13 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161660 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 8.00E-18 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161660 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7776054 7.00E-69 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161660 MYB 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs9399137 3.00E-36 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_001161660 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Platelet Count rs9399137 1.00E-09 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_001161660 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9373124 7.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161660 MYB 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs9373124 1.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001161660 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4895441 7.00E-86 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161660 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs4895441 2.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001161660 MYB 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs9376092 2.00E-11 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_001161660 MYB 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9402686 7.00E-42 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001161660 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs9494145 3.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161660 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Count rs9483788 1.00E-47 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161660 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs9483788 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001161660 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 1.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161660 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 3.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161660 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 6.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_001161683 OTOA 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs8050407 2.20E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001161707 KIRREL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4935969 1.89E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001161707 KIRREL3 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs4935969 4.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001161707 KIRREL3 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs1557488 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001161707 KIRREL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs1557488 7.69E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_001161707 KIRREL3 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Insulin-Like Growth Factor I rs1939992 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001161707 KIRREL3 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs620875 3.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001161725 PPP2R5C 20663923 http://www.ncbi.nlm.nih.gov/pubmed/20663923 Autistic Disorder rs7142002 3.00E-06 A genome-wide scan for common alleles affecting risk for autism. NHGRI|-1
NM_001161726 PPP2R5C 20663923 http://www.ncbi.nlm.nih.gov/pubmed/20663923 Autistic Disorder rs7142002 3.00E-06 A genome-wide scan for common alleles affecting risk for autism. NHGRI|-1
NM_001161814 DAOA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9301037 4.12E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001161814 DAOA 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs4996815 1.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001161814 DAOA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs16968122 6.21E-06 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001161814 DAOA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs12428682 1.65E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001161814 DAOA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs9586708 1.74E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001161814 DAOA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7139453 1.34E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001161814 DAOA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs4632004 1.30E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001161834 C7orf72 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs7805803 9.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001161834 C7orf72 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs1456893 5.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001161834 C7orf72 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs4917014 3.00E-23 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_001161834 C7orf72 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs10276619 3.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_001161841 SULF2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4810663 1.93E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001161841 SULF2 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs4810685 7.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_001161841 SULF2 20173747 http://www.ncbi.nlm.nih.gov/pubmed/20173747 Atrial Fibrillation rs13038095 2.00E-07 Common variants in KCNN3 are associated with lone atrial fibrillation. NHGRI|-1
NM_001162422 ETS1 20169177 http://www.ncbi.nlm.nih.gov/pubmed/20169177 "Lupus Erythematosus, Systemic" rs1128334 2.00E-11 Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus. NHGRI|-1
NM_001162422 ETS1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs11221332 5.00E-16 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001162422 ETS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs11221064 1.60E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001162422 ETS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7130878 1.66E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001162422 ETS1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs6590322 9.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_001162422 ETS1 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs6590330 2.00E-25 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_001162426 TSC1 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs1076160 6.00E-06 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NM_001162427 TSC1 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs1076160 6.00E-06 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NM_001162429 PDCD6IP 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs11714343 9.59E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001162429 PDCD6IP 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1919624 4.01E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001162501 TNRC6B 19117981 http://www.ncbi.nlm.nih.gov/pubmed/19117981 Prostatic Neoplasms rs9623117 5.00E-07 Sequence variants at 22q13 are associated with prostate cancer risk. NHGRI|-1
NM_001162501 TNRC6B 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs12484776 3.00E-12 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_001162501 TNRC6B 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Body Height rs139909 2.00E-07 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_001162501 TNRC6B 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs6001877 7.17E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001162900 TMEM217 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs262929 1.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001163315 FBXL17 21700879 http://www.ncbi.nlm.nih.gov/pubmed/21700879 Adiponectin rs10447248 5.00E-08 Novel Locus FER Is Associated With Serum HMW Adiponectin Levels. NHGRI|-1
NM_001163334 SYTL5 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs872690 9.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001163334 SYTL5 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs761913 5.02E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001163335 SYTL5 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs872690 9.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001163335 SYTL5 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs761913 5.02E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001163377 QPCTL 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2287019 2.00E-16 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001163474 ZNF746 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs855913 4.00E-08 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001163558 PRL 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs1341239 4.00E-06 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_001163558 PRL 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs4236016 4.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001163673 WDR81 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs12150338 7.00E-07 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_001163771 COL11A2 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs2254287 5.00E-08 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001163809 WDR81 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs12150338 7.00E-07 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_001163811 WDR81 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs12150338 7.00E-07 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_001163941 ABCB5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2709748 1.38E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001163941 ABCB5 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs10950821 7.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001163942 ABCB5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2709748 1.38E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001163942 ABCB5 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs10950821 7.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001163989 RAB37 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs10512597 8.00E-11 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_001163990 RAB37 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs10512597 8.00E-11 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_001163991 FAM170A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs184497 6.86E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001163993 ABCB5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2709748 1.38E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001163993 ABCB5 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs10950821 7.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001163999 MECOM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs16852880 9.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001164000 MECOM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs16852880 9.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001164097 VCAN 20516156 http://www.ncbi.nlm.nih.gov/pubmed/20516156 "Depressive Disorder, Major" rs310501 7.00E-06 Genome-wide association study of major recurrent depression in the U.K. population. NHGRI|-1
NM_001164098 VCAN 20516156 http://www.ncbi.nlm.nih.gov/pubmed/20516156 "Depressive Disorder, Major" rs310501 7.00E-06 Genome-wide association study of major recurrent depression in the U.K. population. NHGRI|-1
NM_001164144 ZNF828 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3813131 1.05E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001164144 ZNF828 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3813133 1.67E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001164144 ZNF828 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7316983 1.05E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001164145 ZNF828 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3813131 1.05E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001164145 ZNF828 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3813133 1.67E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001164145 ZNF828 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7316983 1.05E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001164165 ASB3 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Hemoglobins rs1160297 1.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001164165 ASB3 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Hemoglobins rs2357013 6.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001164239 DHX16 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130000 2.38E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001164281 TRAF3IP2 20953186 http://www.ncbi.nlm.nih.gov/pubmed/20953186 "Arthritis, Psoriatic" rs33980500 1.00E-20 Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. NHGRI|-1
NM_001164281 TRAF3IP2 20953188 http://www.ncbi.nlm.nih.gov/pubmed/20953188 Psoriasis rs33980500 1.00E-16 Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. NHGRI|-1
NM_001164282 TRAF3IP2 20953186 http://www.ncbi.nlm.nih.gov/pubmed/20953186 "Arthritis, Psoriatic" rs33980500 1.00E-20 Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. NHGRI|-1
NM_001164282 TRAF3IP2 20953188 http://www.ncbi.nlm.nih.gov/pubmed/20953188 Psoriasis rs33980500 1.00E-16 Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. NHGRI|-1
NM_001164283 TRAF3IP2 20953186 http://www.ncbi.nlm.nih.gov/pubmed/20953186 "Arthritis, Psoriatic" rs33980500 1.00E-20 Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. NHGRI|-1
NM_001164283 TRAF3IP2 20953188 http://www.ncbi.nlm.nih.gov/pubmed/20953188 Psoriasis rs33980500 1.00E-16 Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. NHGRI|-1
NM_001164317 FLNB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4681795 1.70E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001164318 FLNB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4681795 1.70E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001164319 FLNB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4681795 1.70E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001164380 STAU2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs12679254 2.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001164380 STAU2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs10283372 1.90E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001164381 STAU2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs12679254 2.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001164381 STAU2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs10283372 1.90E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001164382 STAU2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs12679254 2.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001164382 STAU2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs10283372 1.90E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001164383 STAU2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs12679254 2.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001164383 STAU2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs10283372 1.90E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001164384 STAU2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs12679254 2.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001164384 STAU2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs10283372 1.90E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001164385 STAU2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs12679254 2.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001164385 STAU2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs10283372 1.90E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001164391 MTF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10874753 4.57E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001164391 MTF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs660870 3.16E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001164391 MTF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs521428 4.57E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001164392 MTF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10874753 4.57E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001164392 MTF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs660870 3.16E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001164392 MTF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs521428 4.57E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001164393 MTF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10874753 4.57E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001164393 MTF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs660870 3.16E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001164393 MTF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs521428 4.57E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001164399 C14orf38 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11158264 2.54E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001164436 TMEM212 21701570 http://www.ncbi.nlm.nih.gov/pubmed/21701570 Body Mass Index rs6794092 2.00E-06 Genome-Wide Association of BMI in African Americans. NHGRI|-1
NM_001164443 ANKRD31 18802019 http://www.ncbi.nlm.nih.gov/pubmed/18802019 "Cholesterol, LDL" rs7703051 1.00E-08 Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. NHGRI|-1
NM_001164460 MGC87042 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs17364464 4.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001164473 FNBP1L 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs237438 5.24E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001164473 FNBP1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs237425 9.56E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001164537 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164537 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164537 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164537 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164538 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164538 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164538 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164538 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164539 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164539 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164539 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164539 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164540 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164540 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164540 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164540 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164541 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164541 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164541 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164541 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164542 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164542 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164542 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164542 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164544 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164544 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164544 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164544 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164545 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164545 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164545 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164545 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164546 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164546 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164546 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164546 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164547 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164547 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164547 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164547 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164548 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164548 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164548 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164548 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164549 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164549 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164549 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164549 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164551 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164551 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164551 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164551 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164552 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164552 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164552 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164552 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164553 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164553 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164553 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164553 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164554 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164554 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164554 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164554 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164555 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_001164555 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_001164555 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001164555 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001164595 PDZRN4 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1458175 2.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001164595 PDZRN4 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1458175 7.90E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001164595 PDZRN4 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2220999 1.09E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001164595 PDZRN4 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 "Cholesterol, HDL" rs871392 3.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001164595 PDZRN4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11532502 1.30E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001164595 PDZRN4 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10880174 5.06E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001164595 PDZRN4 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10785303 5.06E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001164595 PDZRN4 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs1472402 8.20E-06 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001164595 PDZRN4 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs978797 3.38E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001164595 PDZRN4 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Alkaline Phosphatase rs1880887 1.00E-10 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001164605 FXYD5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2285515 7.66E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001164664 MAST4 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1030231 9.35E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001164664 MAST4 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Nonalcoholic Fatty Liver Disease rs1697137 2.00E-06 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_001164664 MAST4 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs10514995 1.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001164664 MAST4 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs10069397 5.00E-08 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001164665 KIAA1549 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12670097 2.85E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001164665 KIAA1549 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12670097 9.68E-06 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001164674 SUMF1 20802204 http://www.ncbi.nlm.nih.gov/pubmed/20802204 Multiple Sclerosis rs794185 6.00E-07 Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. NHGRI|-1
NM_001164675 SUMF1 20802204 http://www.ncbi.nlm.nih.gov/pubmed/20802204 Multiple Sclerosis rs794185 6.00E-07 Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. NHGRI|-1
NM_001164680 CCR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9990343 2.76E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001164680 CCR3 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs9990343 4.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001164680 CCR3 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs6441961 3.00E-07 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_001164688 RD3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10863899 1.67E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001164694 IYD 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs9372078 5.00E-07 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_001164694 IYD 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Carbohydrates rs1591830 1.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_001164695 IYD 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs9372078 5.00E-07 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_001164695 IYD 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Carbohydrates rs1591830 1.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_001164720 CC2D2A 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1861050 8.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001164746 RASSF8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4963910 8.37E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001164747 RASSF8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4963910 8.37E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001164748 RASSF8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4963910 8.37E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001164749 NPAS3 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Mental Disorders rs4982029 4.00E-06 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_001164749 NPAS3 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs8015959 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001164749 NPAS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs8014514 1.79E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001164749 NPAS3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17555909 6.53E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001164749 NPAS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17571355 2.92E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001164749 NPAS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs10142154 2.34E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001164750 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900493 6.94E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164750 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483170 5.79E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164750 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483172 6.77E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164751 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900493 6.94E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164751 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483170 5.79E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164751 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483172 6.77E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164752 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900493 6.94E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164752 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483170 5.79E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164752 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483172 6.77E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164753 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900493 6.94E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164753 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483170 5.79E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164753 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483172 6.77E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164754 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900493 6.94E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164754 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483170 5.79E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164754 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483172 6.77E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164755 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900493 6.94E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164755 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483170 5.79E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164755 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483172 6.77E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164756 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900493 6.94E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164756 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483170 5.79E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164756 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483172 6.77E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001164757 NOS1AP 20062061 http://www.ncbi.nlm.nih.gov/pubmed/20062061 Electrocardiography rs1415259 7.00E-10 Genetic variation in SCN10A influences cardiac conduction. NHGRI|-1
NM_001164757 NOS1AP 16648850 http://www.ncbi.nlm.nih.gov/pubmed/16648850 Electrocardiography rs10494366 1.00E-10 A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. NHGRI|-1
NM_001164757 NOS1AP 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs10494366 5.00E-22 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001164757 NOS1AP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12140791 5.12E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001164757 NOS1AP 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs16857031 1.00E-34 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001164757 NOS1AP 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12029454 3.00E-45 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001164757 NOS1AP 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs4657178 7.00E-33 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001164757 NOS1AP 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs2880058 2.00E-10 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001164757 NOS1AP 19587794 http://www.ncbi.nlm.nih.gov/pubmed/19587794 "Arrhythmias, Cardiac" rs12143842 1.00E-83 Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies. NHGRI|-1
NM_001164757 NOS1AP 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12143842 2.00E-78 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001164757 NOS1AP 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs12143842 2.00E-78 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001164766 ZFHX3 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs16971384 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001164766 ZFHX3 19132087 http://www.ncbi.nlm.nih.gov/pubmed/19132087 Mucocutaneous Lymph Node Syndrome rs7199343 2.00E-06 A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease. NHGRI|-1
NM_001164766 ZFHX3 19597491 http://www.ncbi.nlm.nih.gov/pubmed/19597491 Atrial Fibrillation rs7193343 1.00E-10 A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. NHGRI|-1
NM_001164766 ZFHX3 19597492 http://www.ncbi.nlm.nih.gov/pubmed/19597492 Atrial Fibrillation rs2106261 2.00E-15 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. NHGRI|-1
NM_001164771 SLC7A2 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs2720508 7.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001164883 CTNNA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12471455 9.45E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001164883 CTNNA2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Interleukin-10 rs11695685 5.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001164883 CTNNA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13423141 8.74E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001164883 CTNNA2 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs13409348 3.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001164883 CTNNA2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs399885 5.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001164883 CTNNA2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs7570469 6.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001165032 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12333130 5.60E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001165032 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1003024 6.43E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001165032 RNF182 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs1003024 7.51E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_001165032 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1555051 7.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001165032 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs7750009 7.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001165033 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12333130 5.60E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001165033 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1003024 6.43E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001165033 RNF182 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs1003024 7.51E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_001165033 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1555051 7.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001165033 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs7750009 7.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001165034 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12333130 5.60E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001165034 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1003024 6.43E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001165034 RNF182 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs1003024 7.51E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_001165034 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1555051 7.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001165034 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs7750009 7.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001165035 FBLN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17793957 1.85E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001165035 FBLN2 21368711 http://www.ncbi.nlm.nih.gov/pubmed/21368711 Personality rs9846232 1.00E-08 Genome-wide association study of personality traits in bipolar patients. NHGRI|-1
NM_001165255 MNX1 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs6966038 4.00E-07 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_001165255 MNX1 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs6966038 5.00E-07 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_001165257 SCG3 20159242 http://www.ncbi.nlm.nih.gov/pubmed/20159242 Asthma rs17525472 2.00E-06 Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. NHGRI|-1
NM_001165412 NFKB1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs7665090 4.00E-12 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001165414 LDHA 21124955 http://www.ncbi.nlm.nih.gov/pubmed/21124955 Serum Amyloid A Protein rs2896526 4.00E-22 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. NHGRI|-1
NM_001165415 LDHA 21124955 http://www.ncbi.nlm.nih.gov/pubmed/21124955 Serum Amyloid A Protein rs2896526 4.00E-22 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. NHGRI|-1
NM_001165416 LDHA 21124955 http://www.ncbi.nlm.nih.gov/pubmed/21124955 Serum Amyloid A Protein rs2896526 4.00E-22 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. NHGRI|-1
NM_001165893 NPAS3 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Mental Disorders rs4982029 4.00E-06 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_001165893 NPAS3 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs8015959 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001165893 NPAS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs8014514 1.79E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001165893 NPAS3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17555909 6.53E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001165893 NPAS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17571355 2.92E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001165893 NPAS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs10142154 2.34E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001165899 PDE4D 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs10052657 2.00E-19 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001165899 PDE4D 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs1823068 3.00E-08 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_001165899 PDE4D 17667963 http://www.ncbi.nlm.nih.gov/pubmed/17667963 Neurotic Disorders rs702543 2.00E-06 A whole genome association study of neuroticism using DNA pooling. NHGRI|-1
NM_001165899 PDE4D 19426955 http://www.ncbi.nlm.nih.gov/pubmed/19426955 Asthma rs1588265 3.00E-08 Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. NHGRI|-1
NM_001165920 SERPINF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1057355 4.40E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001165921 SERPINF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1057355 4.40E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001165923 HNF1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2107133 8.77E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001165923 HNF1B 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs4430796 2.00E-06 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001165923 HNF1B 21499250 http://www.ncbi.nlm.nih.gov/pubmed/21499250 Endometrial Neoplasms rs4430796 7.00E-10 Genome-wide association study identifies a common variant associated with risk of endometrial cancer. NHGRI|-1
NM_001165923 HNF1B 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs4430796 6.00E-11 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001165923 HNF1B 17603485 http://www.ncbi.nlm.nih.gov/pubmed/17603485 Prostatic Neoplasms rs4430796 1.00E-11 "Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetes." NHGRI|-1
NM_001165923 HNF1B 18264096 http://www.ncbi.nlm.nih.gov/pubmed/18264096 Prostatic Neoplasms rs4430796 1.00E-09 Multiple loci identified in a genome-wide association study of prostate cancer. NHGRI|-1
NM_001165923 HNF1B 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs4430796 8.00E-06 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_001165923 HNF1B 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs7501939 1.00E-12 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_001165923 HNF1B 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs7501939 2.00E-06 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_001165923 HNF1B 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs7501939 3.00E-18 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001165923 HNF1B 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs7501939 9.00E-12 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_001165924 EMX2 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs2184898 3.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001165933 RGS9 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs8068707 2.40E-06 NBL-GWAS version 1 dbGaP|2845
NM_001165946 IDE 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs6583826 7.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_001165946 IDE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11186960 8.74E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001165958 GSDMB 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs2305480 1.00E-07 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_001165958 GSDMB 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs2305480 3.00E-08 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_001165958 GSDMB 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2290400 6.00E-13 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001165958 GSDMB 17611496 http://www.ncbi.nlm.nih.gov/pubmed/17611496 Asthma rs7216389 9.00E-11 Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. NHGRI|-1
NM_001165958 GSDMB 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs2872507 9.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001165958 GSDMB 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2872507 5.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001165958 GSDMB 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2872507 5.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001165958 GSDMB 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs8067378 1.00E-07 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_001165959 GSDMB 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs2305480 1.00E-07 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_001165959 GSDMB 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs2305480 3.00E-08 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_001165959 GSDMB 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2290400 6.00E-13 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001165959 GSDMB 17611496 http://www.ncbi.nlm.nih.gov/pubmed/17611496 Asthma rs7216389 9.00E-11 Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. NHGRI|-1
NM_001165959 GSDMB 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs2872507 9.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001165959 GSDMB 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2872507 5.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001165959 GSDMB 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2872507 5.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001165959 GSDMB 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs8067378 1.00E-07 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_001165962 ELAC2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3944086 6.41E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001165972 NRG3 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs4933824 2.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001165972 NRG3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2250544 9.03E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001165972 NRG3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2494028 5.41E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001165972 NRG3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2249075 1.47E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001165972 NRG3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2820096 1.33E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001165972 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17689242 5.66E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001165972 NRG3 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs2224865 9.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_001165972 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs2224865 9.98E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_001165972 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11200376 6.80E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001165972 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11200394 6.80E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001165972 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12220373 6.80E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001165972 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11200700 1.00E-04 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001165972 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7068193 6.40E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001165972 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4615965 8.65E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001165972 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7906877 8.92E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001165972 NRG3 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1484170 1.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001165972 NRG3 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Nonalcoholic Fatty Liver Disease rs588517 8.00E-06 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_001165973 NRG3 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs4933824 2.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001165973 NRG3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2250544 9.03E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001165973 NRG3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2494028 5.41E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001165973 NRG3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2249075 1.47E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001165973 NRG3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2820096 1.33E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001165973 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17689242 5.66E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001165973 NRG3 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs2224865 9.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_001165973 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs2224865 9.98E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_001165973 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11200376 6.80E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001165973 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11200394 6.80E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001165973 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12220373 6.80E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001165973 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11200700 1.00E-04 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001165973 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7068193 6.40E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001165973 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4615965 8.65E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001165973 NRG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7906877 8.92E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001165973 NRG3 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1484170 1.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001165973 NRG3 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Nonalcoholic Fatty Liver Disease rs588517 8.00E-06 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_001165979 PLCE1 21368711 http://www.ncbi.nlm.nih.gov/pubmed/21368711 Religion and Psychology rs9419788 4.00E-08 Genome-wide association study of personality traits in bipolar patients. NHGRI|-1
NM_001165979 PLCE1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs11187837 4.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001165979 PLCE1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs3765524 2.00E-09 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001165979 PLCE1 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs117607728 4.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001165979 PLCE1 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs2274223 4.00E-20 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001165979 PLCE1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs3781264 4.00E-09 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001165979 PLCE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs3781264 2.31E-04 Genome-wide association between genotype and incident stroke in participants of primarily self-described European ancestry dbGaP|2886
NM_001166010 PECI 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs6942328 1.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_001166018 POU6F2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs9655034 8.80E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001166018 POU6F2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs859522 3.41E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001166104 NR3C2 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Fibrinogen rs1490453 3.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001166108 PALLD 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs17054392 3.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001166108 PALLD 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs2710833 6.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001166109 PALLD 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs17054392 3.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001166109 PALLD 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs2710833 6.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001166110 PALLD 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs17054392 3.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001166110 PALLD 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs2710833 6.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001166119 LEF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17038960 3.00E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001166133 FRAS1 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs1268789 7.00E-08 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001166139 LCORL 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs16896068 2.00E-13 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001166139 LCORL 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs6830062 1.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001166139 LCORL 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs6830062 5.00E-09 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001166139 LCORL 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs6830062 8.00E-06 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_001166220 TBX20 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs1362212 1.00E-13 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001166220 TBX20 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs2392362 2.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001166220 TBX20 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Liver Cirrhosis rs343064 3.00E-08 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001166220 TBX20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs74992754 6.07E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001166226 CEP120 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs2115172 2.00E-06 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001166226 CEP120 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs17470137 1.00E-11 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_001166243 FHIT 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs1825630 8.00E-06 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_001166243 FHIT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs3912494 9.80E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001166243 FHIT 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs10510837 4.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_001166243 FHIT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1735460 3.40E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001166243 FHIT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1735460 3.67E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001166243 FHIT 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs6791644 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001166243 FHIT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9825823 2.13E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001166243 FHIT 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs10514718 4.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_001166243 FHIT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2121794 2.14E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001166247 GRIK2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1361168 7.90E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001166247 GRIK2 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Fibrinogen rs12207601 2.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001166247 GRIK2 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs4520040 3.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001166252 LPPR4 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs7543130 1.00E-07 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_001166261 MTIF3 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs4771122 9.00E-10 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001166261 MTIF3 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7336332 1.00E-06 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001166261 MTIF3 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs9512730 5.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_001166261 MTIF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1218897 2.49E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166261 MTIF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1218885 4.54E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166262 MTIF3 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs4771122 9.00E-10 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001166262 MTIF3 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7336332 1.00E-06 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001166262 MTIF3 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs9512730 5.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_001166262 MTIF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1218897 2.49E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166262 MTIF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1218885 4.54E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166263 MTIF3 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs4771122 9.00E-10 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001166263 MTIF3 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7336332 1.00E-06 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001166263 MTIF3 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs9512730 5.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_001166263 MTIF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1218897 2.49E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166263 MTIF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1218885 4.54E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166264 LTBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4670322 5.13E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001166264 LTBP1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs3769528 8.00E-08 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001166264 LTBP1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs41464348 7.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001166265 LTBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4670322 5.13E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001166265 LTBP1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs3769528 8.00E-08 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001166265 LTBP1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs41464348 7.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001166271 SPATA13 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2793483 3.78E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001166271 SPATA13 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17464589 2.84E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001166271 SPATA13 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs17079773 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001166276 ARHGAP25 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs10496166 4.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001166277 ARHGAP25 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs10496166 4.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001166290 KCNJ11 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs5215 4.00E-07 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001166290 KCNJ11 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs5215 5.00E-11 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001166290 KCNJ11 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs5219 1.00E-07 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001166290 KCNJ11 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs5219 1.00E-09 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001166290 KCNJ11 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs5219 5.00E-07 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001166290 KCNJ11 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs5219 7.00E-11 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001166293 SSX2IP 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9729377 6.00E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001166294 SSX2IP 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9729377 6.00E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001166295 SSX2IP 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9729377 6.00E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001166305 TMEM44 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs789852 7.00E-07 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001166306 TMEM44 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs789852 7.00E-07 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001166373 1-Mar 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs3792615 9.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_001166392 TPBG 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2917494 5.90E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001166412 SMOC2 19890347 http://www.ncbi.nlm.nih.gov/pubmed/19890347 Vitiligo rs13208776 9.00E-08 "Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8." NHGRI|-1
NM_001166412 SMOC2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7741751 2.25E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001166415 EHHADH 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs7374394 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001166415 EHHADH 21042317 http://www.ncbi.nlm.nih.gov/pubmed/21042317 "Depressive Disorder, Major" rs7647854 5.00E-06 "Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned." NHGRI|-1
NM_001166417 SSX2IP 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9729377 6.00E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001166434 ITIH1 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs1042779 2.00E-07 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001166435 ITIH1 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs1042779 2.00E-07 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001166436 ITIH1 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs1042779 2.00E-07 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001166451 KNG1 20303064 http://www.ncbi.nlm.nih.gov/pubmed/20303064 Partial Thromboplastin Time rs710446 1.00E-21 "Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time." NHGRI|-1
NM_001166451 KNG1 20876611 http://www.ncbi.nlm.nih.gov/pubmed/20876611 Adiponectin rs11924390 2.00E-09 Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ. NHGRI|-1
NM_001166504 ADH7 21437268 http://www.ncbi.nlm.nih.gov/pubmed/21437268 Head and Neck Neoplasms rs971074 9.00E-17 A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. NHGRI|-1
NM_001166504 ADH7 19609347 http://www.ncbi.nlm.nih.gov/pubmed/19609347 Hypertension rs991316 5.00E-06 A genome-wide association study of hypertension and blood pressure in African Americans. NHGRI|-1
NM_001166533 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7730742 9.29E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166533 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10035707 5.09E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166533 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs957459 4.21E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166533 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2619046 1.76E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166533 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs162096 3.33E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166534 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7730742 9.29E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166534 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10035707 5.09E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166534 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs957459 4.21E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166534 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2619046 1.76E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166534 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs162096 3.33E-05 NBL-GWAS version 2 dbGaP|2895
NM_001166538 LST1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9267502 3.79E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001166598 APOA5 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs2266788 5.00E-13 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001166598 APOA5 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2266788 2.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001166598 APOA5 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2266788 2.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001166598 APOA5 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2266788 4.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001166598 APOA5 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs1263173 2.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001166598 APOA5 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Triglycerides rs7396835 1.00E-09 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001166624 CFHR3 20694013 http://www.ncbi.nlm.nih.gov/pubmed/20694013 Meningococcal Infections rs426736 5.00E-13 Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. NHGRI|-1
NM_001166691 TTK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7453746 7.12E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001166691 TTK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7453746 7.86E-06 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001166692 C11orf91 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs831620 3.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001166692 C11orf91 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2746600 8.29E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001166693 AFF1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs442177 3.00E-10 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001166694 CHRNA3 18978790 http://www.ncbi.nlm.nih.gov/pubmed/18978790 Lung Neoplasms rs1051730 1.00E-15 Lung cancer susceptibility locus at 5p15.33. NHGRI|-1
NM_001166694 CHRNA3 19836008 http://www.ncbi.nlm.nih.gov/pubmed/19836008 Lung Neoplasms rs1051730 2.00E-51 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. NHGRI|-1
NM_001166694 CHRNA3 20418889 http://www.ncbi.nlm.nih.gov/pubmed/20418889 Smoking rs1051730 2.00E-66 Meta-analysis and imputation refines the association of 15q25 with smoking quantity. NHGRI|-1
NM_001166694 CHRNA3 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs1051730 2.00E-69 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_001166694 CHRNA3 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs1051730 3.00E-73 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001166694 CHRNA3 18385739 http://www.ncbi.nlm.nih.gov/pubmed/18385739 Tobacco Use Disorder rs1051730 6.00E-20 "A variant associated with nicotine dependence, lung cancer and peripheral arterial disease." NHGRI|-1
NM_001166694 CHRNA3 18978787 http://www.ncbi.nlm.nih.gov/pubmed/18978787 Lung Neoplasms rs8042374 8.00E-12 Common 5p15.33 and 6p21.33 variants influence lung cancer risk. NHGRI|-1
NM_001166698 FAM13C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10509101 3.95E-05 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_001167575 C9orf82 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10453196 3.37E-06 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001167575 C9orf82 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10491819 5.58E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001167575 C9orf82 19483685 http://www.ncbi.nlm.nih.gov/pubmed/19483685 Drug-Induced Liver Injury rs10812428 1.00E-06 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. NHGRI|-1
NM_001167575 C9orf82 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12236180 4.63E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001167575 C9orf82 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs1889899 6.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001167576 TRPC7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2673926 8.27E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001167576 TRPC7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2673925 7.34E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001167576 TRPC7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2673913 8.51E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001167577 TRPC7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2673926 8.27E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001167577 TRPC7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2673925 7.34E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001167577 TRPC7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2673913 8.51E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001167579 SLC34A1 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs6420094 1.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001167580 SV2B 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Sphingomyelins rs886144 2.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_001167582 RBM6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2681779 6.15E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001167582 RBM6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2624821 6.07E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001167582 RBM6 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs6762477 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001167583 ZFAT 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1036819 1.00E-24 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001167583 ZFAT 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs12680655 2.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001167583 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1545240 1.52E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001167583 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs16905215 1.89E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001167583 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs9785140 1.26E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001167608 RHBDD1 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Forced Expiratory Volume rs3820928 5.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_001167623 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001167623 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001167623 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001167623 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001167624 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001167624 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001167624 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001167624 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001167625 CACNA1C 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1006737 3.00E-08 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001167625 CACNA1C 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1006737 7.00E-08 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001167625 CACNA1C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs886898 1.05E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001167625 CACNA1C 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs216013 9.00E-07 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001167667 CDH18 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs349475 2.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_001167671 LPP 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1464510 3.00E-40 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001167671 LPP 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs1464510 5.00E-09 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_001167671 LPP 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs1464510 1.00E-11 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_001167671 LPP 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Mass Index rs1152846 3.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001167671 LPP 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs1152846 6.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001167672 LPP 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1464510 3.00E-40 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001167672 LPP 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs1464510 5.00E-09 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_001167672 LPP 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs1464510 1.00E-11 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_001167672 LPP 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Mass Index rs1152846 3.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001167672 LPP 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs1152846 6.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001167674 CADM2 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs13078807 4.00E-11 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001167674 CADM2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7642134 4.00E-10 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001167674 CADM2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4574309 5.23E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001167674 CADM2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4396907 6.68E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001167674 CADM2 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs10511089 7.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001167675 CADM2 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs13078807 4.00E-11 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001167675 CADM2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7642134 4.00E-10 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001167675 CADM2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4574309 5.23E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001167675 CADM2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4396907 6.68E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001167675 CADM2 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs10511089 7.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001167681 FLI1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs588407 3.45E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264303 7.62E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264302 7.39E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264301 7.62E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264298 7.62E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9262288 6.65E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111872682 6.72E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs75893422 8.03E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113373192 6.65E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2517467 2.25E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2517467 8.78E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2074506 5.71E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs753725 2.01E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs753725 1.05E-05 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2532938 7.71E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167733 VARS2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs4678 4.59E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2532934 2.37E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2532934 8.78E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001167733 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2532929 1.51E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264303 7.62E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264302 7.39E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264301 7.62E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264298 7.62E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9262288 6.65E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111872682 6.72E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs75893422 8.03E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113373192 6.65E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2517467 2.25E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2517467 8.78E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2074506 5.71E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs753725 2.01E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs753725 1.05E-05 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2532938 7.71E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs4678 4.59E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2532934 2.37E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2532934 8.78E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001167734 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2532929 1.51E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001167738 NAV1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1854077 4.46E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001167738 NAV1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs614452 1.02E-04 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001167738 NAV1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs16865416 5.11E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001167738 NAV1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs545372 8.92E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001167738 NAV1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs625436 8.92E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001167738 NAV1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs495198 2.19E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001167740 SMYD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2275313 6.98E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001167740 SMYD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4654179 6.53E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001167740 SMYD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4654180 3.68E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001167740 SMYD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2105158 2.06E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001167741 MTX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7735699 1.78E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001167741 MTX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs265010 2.67E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001167827 TFEB 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2842643 3.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_001167856 SBNO1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs11830103 4.00E-15 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001167867 ATP5SL 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs17318596 5.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001167868 ATP5SL 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs17318596 5.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001167869 ATP5SL 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs17318596 5.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001167871 ATP5SL 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs17318596 5.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001167882 ANKRD50 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs1986655 2.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_001167911 VEPH1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs9866141 9.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001167912 VEPH1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs9866141 9.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001167915 VEPH1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs9866141 9.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001167916 VEPH1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs9866141 9.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001167917 VEPH1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs9866141 9.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001167928 IL1RAP 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs9290936 4.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001167928 IL1RAP 18385676 http://www.ncbi.nlm.nih.gov/pubmed/18385676 Lung Neoplasms rs7626795 8.00E-06 Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. NHGRI|-1
NM_001167929 IL1RAP 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs9290936 4.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001167929 IL1RAP 18385676 http://www.ncbi.nlm.nih.gov/pubmed/18385676 Lung Neoplasms rs7626795 8.00E-06 Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. NHGRI|-1
NM_001167930 IL1RAP 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs9290936 4.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001167930 IL1RAP 18385676 http://www.ncbi.nlm.nih.gov/pubmed/18385676 Lung Neoplasms rs7626795 8.00E-06 Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. NHGRI|-1
NM_001167931 IL1RAP 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs9290936 4.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001167931 IL1RAP 18385676 http://www.ncbi.nlm.nih.gov/pubmed/18385676 Lung Neoplasms rs7626795 8.00E-06 Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. NHGRI|-1
NM_001167940 CADPS2 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs2429582 6.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001167945 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 1.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001167945 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 7.00E-07 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001167945 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs11014166 6.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001167945 CACNB2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Blood Pressure rs7069923 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001167945 CACNB2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 C-Reactive Protein rs7076247 6.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001167945 CACNB2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17661538 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001167945 CACNB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4748442 9.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001167959 TMEM178 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs2716734 2.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001167959 TMEM178 18957941 http://www.ncbi.nlm.nih.gov/pubmed/18957941 Personality rs2540226 3.00E-06 Genome-wide association scan for five major dimensions of personality. NHGRI|-1
NM_001167961 KCTD7 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs10263935 4.00E-07 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_001167965 WDR65 21460395 http://www.ncbi.nlm.nih.gov/pubmed/21460395 Telomere length rs621559 2.00E-06 A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer. NHGRI|-1
NM_001167966 WDR65 21460395 http://www.ncbi.nlm.nih.gov/pubmed/21460395 Telomere length rs621559 2.00E-06 A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer. NHGRI|-1
NM_001168271 GPR156 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs9289143 3.03E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001168271 GPR156 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs9289143 8.56E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001168272 ITPR1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs746039 2.06E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001168278 WWTR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10513355 4.66E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001168280 WWTR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10513355 4.66E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001168298 CXCR2 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs11676348 1.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001168299 KLHL13 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs2430212 2.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001168300 KLHL13 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs2430212 2.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001168301 KLHL13 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs2430212 2.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001168302 KLHL13 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs2430212 2.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001168303 KLHL13 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs2430212 2.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001168319 EDN1 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs1040994 2.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001168335 ME2 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs732528 7.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252109 3.07E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs14224 3.04E-19 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252117 3.07E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252120 4.79E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252125 1.55E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252126 1.06E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252130 3.57E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4252135 1.09E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1247555 1.91E-13 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1247557 1.63E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1620921 2.67E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1740442 1.63E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2115869 5.38E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs783153 2.04E-15 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1937479 3.04E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2465868 1.54E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001168338 PLG 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs935181 9.81E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001168339 TTC39B 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs471364 3.00E-10 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001168339 TTC39B 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs643531 7.00E-09 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001168339 TTC39B 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs1780159 6.00E-06 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_001168340 TTC39B 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs471364 3.00E-10 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001168340 TTC39B 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs643531 7.00E-09 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001168340 TTC39B 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs1780159 6.00E-06 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_001168341 TTC39B 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs471364 3.00E-10 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001168341 TTC39B 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs643531 7.00E-09 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001168341 TTC39B 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs1780159 6.00E-06 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_001168342 TTC39B 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs471364 3.00E-10 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001168342 TTC39B 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs643531 7.00E-09 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001168342 TTC39B 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs1780159 6.00E-06 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_001168344 RREB1 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs11755724 1.00E-06 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_001168344 RREB1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs557074 4.36E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001168344 RREB1 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs675209 1.00E-09 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_001168357 PLA2G7 20442857 http://www.ncbi.nlm.nih.gov/pubmed/20442857 1-Alkyl-2-acetylglycerophosphocholine Esterase rs1805017 6.00E-14 Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study. NHGRI|-1
NM_001168360 PCDH11X 19136949 http://www.ncbi.nlm.nih.gov/pubmed/19136949 Alzheimer Disease rs2573905 2.00E-07 Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease. NHGRI|-1
NM_001168361 PCDH11X 19136949 http://www.ncbi.nlm.nih.gov/pubmed/19136949 Alzheimer Disease rs2573905 2.00E-07 Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease. NHGRI|-1
NM_001168363 PCDH11X 19136949 http://www.ncbi.nlm.nih.gov/pubmed/19136949 Alzheimer Disease rs2573905 2.00E-07 Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease. NHGRI|-1
NM_001168368 GALNTL1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 2.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001168368 GALNTL1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001168374 KIAA0319 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs16889440 2.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_001168375 KIAA0319 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs16889440 2.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_001168376 KIAA0319 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs16889440 2.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_001168377 KIAA0319 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs16889440 2.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_001168388 CITED2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs628751 1.00E-17 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001168388 CITED2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs643381 5.00E-25 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001168388 CITED2 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs642858 2.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_001168388 CITED2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs169291 5.93E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001168389 CITED2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs628751 1.00E-17 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001168389 CITED2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs643381 5.00E-25 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001168389 CITED2 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs642858 2.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_001168389 CITED2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs169291 5.93E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001168393 C5orf41 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs251253 9.00E-13 Genome-wide association study of PR interval. NHGRI|-1
NM_001168394 C5orf41 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs251253 9.00E-13 Genome-wide association study of PR interval. NHGRI|-1
NM_001168647 CNKSR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11094807 2.92E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001168648 CNKSR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11094807 2.92E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001168649 CNKSR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11094807 2.92E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001168724 TMEM135 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1386330 2.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001169117 STIM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12505133 3.78E-05 NBL-GWAS version 2 dbGaP|2895
NM_001169117 STIM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs11727649 1.88E-05 NBL-GWAS version 2 dbGaP|2895
NM_001169118 STIM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12505133 3.78E-05 NBL-GWAS version 2 dbGaP|2895
NM_001169118 STIM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs11727649 1.88E-05 NBL-GWAS version 2 dbGaP|2895
NM_001169122 AFF2 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs5936441 5.00E-06 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_001169122 AFF2 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs2159767 7.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_001169123 AFF2 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs5936441 5.00E-06 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_001169123 AFF2 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs2159767 7.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_001169124 AFF2 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs5936441 5.00E-06 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_001169124 AFF2 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs2159767 7.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_001169125 AFF2 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs5936441 5.00E-06 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_001169125 AFF2 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs2159767 7.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_001170406 CDK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4132554 7.66E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001170407 CDK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4132554 7.66E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001170418 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3135050 2.42E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001170418 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071653 2.34E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001170418 MOG 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal Neoplasms rs29232 9.00E-17 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_001170418 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3131854 2.54E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001170464 CDK17 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs11108495 4.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001170464 CDK17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7312607 9.34E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001170585 PLB1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs2338545 6.34E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001170585 PLB1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2940787 1.92E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001170628 AFF2 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs5936441 5.00E-06 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_001170628 AFF2 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs2159767 7.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_001170637 SRGAP2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2336938 2.83E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001170639 CDK20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10868677 8.79E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001170640 CDK20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10868677 8.79E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001170700 DTHD1 20802204 http://www.ncbi.nlm.nih.gov/pubmed/20802204 Multiple Sclerosis rs13117816 7.00E-06 Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. NHGRI|-1
NM_001170714 BCAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs13337397 6.65E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001170715 BCAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs13337397 6.65E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001170716 BCAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs13337397 6.65E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001170717 BCAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs13337397 6.65E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001170718 BCAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs13337397 6.65E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001170719 BCAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs13337397 6.65E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001170720 BCAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs13337397 6.65E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001170721 BCAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs13337397 6.65E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001170754 C1orf127 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1280975 4.93E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001170765 LCOR 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6584099 4.33E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001170766 LCOR 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6584099 4.33E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001170791 FAM82A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1374196 7.26E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001170791 FAM82A1 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs6741148 4.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001170791 FAM82A1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs4670766 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001170791 FAM82A1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs17511102 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001170791 FAM82A1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs604381 8.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001170791 FAM82A1 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs4670779 4.00E-06 New sequence variants associated with bone mineral density. NHGRI|-1
NM_001170792 FAM82A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1374196 7.26E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001170792 FAM82A1 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs6741148 4.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001170792 FAM82A1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs4670766 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001170792 FAM82A1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs17511102 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001170792 FAM82A1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs604381 8.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001170792 FAM82A1 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs4670779 4.00E-06 New sequence variants associated with bone mineral density. NHGRI|-1
NM_001170793 FAM82A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1374196 7.26E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001170793 FAM82A1 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs6741148 4.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001170793 FAM82A1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs4670766 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001170793 FAM82A1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs17511102 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001170793 FAM82A1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs604381 8.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001170793 FAM82A1 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs4670779 4.00E-06 New sequence variants associated with bone mineral density. NHGRI|-1
NM_001170794 BACH2 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs10806425 4.00E-10 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001170794 BACH2 18840781 http://www.ncbi.nlm.nih.gov/pubmed/18840781 "Diabetes Mellitus, Type 1" rs3757247 1.00E-06 Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes. NHGRI|-1
NM_001170794 BACH2 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs11755527 5.00E-12 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_001170794 BACH2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs11755527 5.00E-08 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001170794 BACH2 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs1847472 5.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001170794 BACH2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1145724 4.14E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001170794 BACH2 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs806276 3.00E-07 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_001170806 C8orf47 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs13278732 6.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_001170905 ZNF736 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, LDL" rs10266483 8.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001170957 SMG6 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs1231206 9.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001170957 SMG6 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs216172 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001170957 SMG6 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs10852932 2.00E-11 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_001171 ABCC6 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2239322 6.84E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001171 ABCC6 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8056397 8.87E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001171025 PTPRD 18660810 http://www.ncbi.nlm.nih.gov/pubmed/18660810 Restless Legs Syndrome rs1975197 6.00E-09 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. NHGRI|-1
NM_001171025 PTPRD 20174558 http://www.ncbi.nlm.nih.gov/pubmed/20174558 "Diabetes Mellitus, Type 2" rs17584499 9.00E-10 A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. NHGRI|-1
NM_001171025 PTPRD 18660810 http://www.ncbi.nlm.nih.gov/pubmed/18660810 Restless Legs Syndrome rs4626664 6.00E-10 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. NHGRI|-1
NM_001171025 PTPRD 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs2475335 9.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_001171025 PTPRD 21647700 http://www.ncbi.nlm.nih.gov/pubmed/21647700 "Diabetes Mellitus, Type 2" rs649891 6.00E-06 "Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals." NHGRI|-1
NM_001171025 PTPRD 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Braces rs1535480 4.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001171025 PTPRD 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7044355 1.00E-07 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001171025 PTPRD 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10815798 6.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001171195 ELAVL2 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs4246856 6.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001171195 ELAVL2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Weight rs2225614 3.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001171195 ELAVL2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10491833 5.28E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001171195 ELAVL2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9406815 9.13E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001171195 ELAVL2 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs12552736 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001171195 ELAVL2 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs13300284 4.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001171195 ELAVL2 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs17774966 8.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001171195 ELAVL2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Waist Circumference rs613391 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001171195 ELAVL2 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Stomach Neoplasms rs10811771 8.00E-07 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_001171197 ELAVL2 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs4246856 6.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001171197 ELAVL2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Weight rs2225614 3.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001171197 ELAVL2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10491833 5.28E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001171197 ELAVL2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9406815 9.13E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001171197 ELAVL2 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs12552736 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001171197 ELAVL2 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs13300284 4.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001171197 ELAVL2 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs17774966 8.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001171197 ELAVL2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Waist Circumference rs613391 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001171197 ELAVL2 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Stomach Neoplasms rs10811771 8.00E-07 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_001171251 C17orf53 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs227584 9.00E-07 New sequence variants associated with bone mineral density. NHGRI|-1
NM_001171506 MCFD2 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs76351433 2.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001171507 MCFD2 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs76351433 2.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001171508 MCFD2 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs76351433 2.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001171509 MCFD2 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs76351433 2.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001171510 MCFD2 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs76351433 2.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001171511 MCFD2 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs76351433 2.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001171581 ITM2A 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1474563 3.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001171622 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001171622 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001171622 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001171622 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001171622 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001171623 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001171623 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001171623 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001171623 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001171623 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001171624 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001171624 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001171624 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001171624 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001171624 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001171625 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001171625 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001171625 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001171625 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001171625 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001171626 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001171626 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001171626 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001171626 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001171626 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001171627 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001171627 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001171627 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001171627 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001171627 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001171628 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001171628 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001171628 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001171628 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001171628 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001171629 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001171629 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001171629 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001171629 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001171629 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001171630 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001171630 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001171630 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001171630 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001171630 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001171713 FBXL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2291897 1.82E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001171795 C8orf83 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs16915399 9.45E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001171795 C8orf83 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6471335 1.33E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001171796 C8orf83 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs16915399 9.45E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001171796 C8orf83 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6471335 1.33E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001171797 C8orf83 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs16915399 9.45E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001171797 C8orf83 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6471335 1.33E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001171798 C8orf83 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs16915399 9.45E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001171798 C8orf83 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6471335 1.33E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001171799 C8orf83 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs16915399 9.45E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001171799 C8orf83 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6471335 1.33E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001171805 PAPD7 18821564 http://www.ncbi.nlm.nih.gov/pubmed/18821564 Attention Deficit Disorder with Hyperactivity rs11134178 3.00E-06 Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder. NHGRI|-1
NM_001171805 PAPD7 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs7729273 1.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001171805 PAPD7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6891243 2.10E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001171806 PAPD7 18821564 http://www.ncbi.nlm.nih.gov/pubmed/18821564 Attention Deficit Disorder with Hyperactivity rs11134178 3.00E-06 Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder. NHGRI|-1
NM_001171806 PAPD7 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs7729273 1.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001171806 PAPD7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6891243 2.10E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001171818 PPARD 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs9658108 5.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001171818 PPARD 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs4713858 4.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001171819 PPARD 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs9658108 5.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001171819 PPARD 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs4713858 4.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001171820 PPARD 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs9658108 5.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001171820 PPARD 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs4713858 4.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001171873 UGT3A1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs860413 1.00E-11 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001171942 GLRA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs3020867 1.46E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001171988 AGA 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11947216 3.31E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001171988 AGA 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10031053 1.54E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001171988 AGA 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs9993819 5.49E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001171988 AGA 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs569945 8.85E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001171988 AGA 17903306 http://www.ncbi.nlm.nih.gov/pubmed/17903306 Heart Rate rs1395479 7.00E-06 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. NHGRI|-1
NM_001171991 HCCS 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs5934953 1.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001171992 C6orf223 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001171992 C6orf223 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001171992 C6orf223 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001171992 C6orf223 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001171992 C6orf223 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001172086 PEX2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7821178 3.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001172086 PEX2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs7846385 5.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001172086 PEX2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs3864663 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001172086 PEX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10091852 8.64E-05 NBL-GWAS version 2 dbGaP|2895
NM_001172087 PEX2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7821178 3.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001172087 PEX2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs7846385 5.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001172087 PEX2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs3864663 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001172087 PEX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10091852 8.64E-05 NBL-GWAS version 2 dbGaP|2895
NM_001172128 IL16 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs7172689 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001172173 CSRNP3 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs6710518 5.00E-10 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_001172218 SCMH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs6686842 2.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001172219 SCMH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs6686842 2.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001172220 SCMH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs6686842 2.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001172221 SCMH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs6686842 2.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001172222 SCMH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs6686842 2.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001172312 PLS1 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs3773506 9.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_001172418 BTBD9 17637780 http://www.ncbi.nlm.nih.gov/pubmed/17637780 Restless Legs Syndrome rs9296249 4.00E-18 Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. NHGRI|-1
NM_001172418 BTBD9 17634447 http://www.ncbi.nlm.nih.gov/pubmed/17634447 Restless Legs Syndrome rs3923809 1.00E-17 A genetic risk factor for periodic limb movements in sleep. NHGRI|-1
NM_001172430 AMPD3 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Bipolar Disorder rs6484218 4.00E-08 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_001172431 AMPD3 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Bipolar Disorder rs6484218 4.00E-08 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_001172509 SATB2 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs1992950 5.00E-06 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_001172509 SATB2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs12617311 6.00E-13 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001172517 SATB2 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs1992950 5.00E-06 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_001172517 SATB2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs12617311 6.00E-13 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001172574 MCPH1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Attention Deficit Disorder with Hyperactivity rs4875598 9.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001172574 MCPH1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7817815 4.96E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001172575 MCPH1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Attention Deficit Disorder with Hyperactivity rs4875598 9.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_001172575 MCPH1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7817815 4.96E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001172646 PLCB4 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs6039424 9.55E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001172646 PLCB4 20172861 http://www.ncbi.nlm.nih.gov/pubmed/20172861 Leukocyte Count rs2072910 3.00E-10 Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count. NHGRI|-1
NM_001172663 RAB40C 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs763014 5.00E-06 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001172664 RAB40C 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs763014 5.00E-06 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001172665 RAB40C 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs763014 5.00E-06 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001172666 RAB40C 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs763014 5.00E-06 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001172672 PNPLA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs5934349 1.75E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001172673 CELF5 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs11669592 4.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001172689 ZNF573 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs16975963 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001172690 ZNF573 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs16975963 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001172691 ZNF573 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs16975963 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001172692 ZNF573 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs16975963 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001172698 PPARGC1B 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs32579 4.00E-06 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_001172699 PPARGC1B 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs32579 4.00E-06 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_001172774 DPY19L3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2012353 2.42E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001172774 DPY19L3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs16967057 2.87E-06 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001172774 DPY19L3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2111504 1.57E-07 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001172774 DPY19L3 19488044 http://www.ncbi.nlm.nih.gov/pubmed/19488044 Bipolar Disorder rs2111504 2.00E-06 Genome-wide association study of bipolar disorder in European American and African American individuals. NHGRI|-1
NM_001172810 DNAI2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs7219585 1.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001172811 SLC30A8 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs13266634 2.00E-14 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001172811 SLC30A8 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs13266634 3.00E-06 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001172811 SLC30A8 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001172811 SLC30A8 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001172811 SLC30A8 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001172811 SLC30A8 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs13266634 6.00E-08 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001172811 SLC30A8 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs13266634 7.00E-06 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001172811 SLC30A8 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs13266634 8.00E-08 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001172811 SLC30A8 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs13266634 5.00E-08 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_001172811 SLC30A8 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs3802177 1.00E-08 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001172811 SLC30A8 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs11558471 3.00E-11 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001172813 SLC30A8 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs13266634 2.00E-14 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001172813 SLC30A8 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs13266634 3.00E-06 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001172813 SLC30A8 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001172813 SLC30A8 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001172813 SLC30A8 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001172813 SLC30A8 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs13266634 6.00E-08 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001172813 SLC30A8 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs13266634 7.00E-06 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001172813 SLC30A8 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs13266634 8.00E-08 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001172813 SLC30A8 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs13266634 5.00E-08 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_001172813 SLC30A8 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs3802177 1.00E-08 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001172813 SLC30A8 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs11558471 3.00E-11 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001172814 SLC30A8 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs13266634 2.00E-14 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001172814 SLC30A8 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs13266634 3.00E-06 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001172814 SLC30A8 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001172814 SLC30A8 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001172814 SLC30A8 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001172814 SLC30A8 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs13266634 6.00E-08 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001172814 SLC30A8 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs13266634 7.00E-06 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001172814 SLC30A8 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs13266634 8.00E-08 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001172814 SLC30A8 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs13266634 5.00E-08 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_001172814 SLC30A8 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs3802177 1.00E-08 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001172814 SLC30A8 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs11558471 3.00E-11 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001172815 SLC30A8 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs13266634 2.00E-14 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001172815 SLC30A8 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs13266634 3.00E-06 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001172815 SLC30A8 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001172815 SLC30A8 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001172815 SLC30A8 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001172815 SLC30A8 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs13266634 6.00E-08 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001172815 SLC30A8 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs13266634 7.00E-06 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001172815 SLC30A8 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs13266634 8.00E-08 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001172815 SLC30A8 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs13266634 5.00E-08 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_001172815 SLC30A8 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs3802177 1.00E-08 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001172815 SLC30A8 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs11558471 3.00E-11 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001172818 PGM1 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2269241 4.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001172818 PGM1 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs2749097 2.00E-09 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_001172818 PGM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11208285 9.59E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001172818 PGM1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2819130 1.23E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001172819 PGM1 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2269241 4.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001172819 PGM1 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs2749097 2.00E-09 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_001172819 PGM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11208285 9.59E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001172819 PGM1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2819130 1.23E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001172831 ZNF300 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs1000113 3.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001172831 ZNF300 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs11747270 3.00E-16 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001172831 ZNF300 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs7714584 8.00E-19 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001172832 ZNF300 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs1000113 3.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001172832 ZNF300 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs11747270 3.00E-16 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001172832 ZNF300 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs7714584 8.00E-19 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001172895 CAV1 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs3807989 4.00E-28 Genome-wide association study of PR interval. NHGRI|-1
NM_001172895 CAV1 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3807989 7.00E-13 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001172895 CAV1 20835238 http://www.ncbi.nlm.nih.gov/pubmed/20835238 "Glaucoma, Open-Angle" rs4236601 2.00E-11 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. NHGRI|-1
NM_001172896 CAV1 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs3807989 4.00E-28 Genome-wide association study of PR interval. NHGRI|-1
NM_001172896 CAV1 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3807989 7.00E-13 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001172896 CAV1 20835238 http://www.ncbi.nlm.nih.gov/pubmed/20835238 "Glaucoma, Open-Angle" rs4236601 2.00E-11 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. NHGRI|-1
NM_001172897 CAV1 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs3807989 4.00E-28 Genome-wide association study of PR interval. NHGRI|-1
NM_001172897 CAV1 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3807989 7.00E-13 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001172897 CAV1 20835238 http://www.ncbi.nlm.nih.gov/pubmed/20835238 "Glaucoma, Open-Angle" rs4236601 2.00E-11 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. NHGRI|-1
NM_001173393 HAVCR1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs1501908 1.00E-11 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001173454 PDHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs5955711 9.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001173455 PDHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs5955711 9.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001173456 PDHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs5955711 9.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001173467 SP7 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2016266 1.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001173467 SP7 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs10876432 1.00E-07 New sequence variants associated with bone mineral density. NHGRI|-1
NM_001173482 CRBN 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4055307 1.85E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001173482 CRBN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9829721 6.83E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001173482 CRBN 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1601875 7.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001173484 NEBL 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs12219125 9.00E-09 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_001173484 NEBL 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs12772794 7.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001173484 NEBL 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs16920624 7.00E-07 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_001173484 NEBL 20610895 http://www.ncbi.nlm.nih.gov/pubmed/20610895 Vascular Diseases rs2359536 2.00E-06 Identification of evidence suggestive of an association with peripheral arterial disease at the OSBPL10 locus by genome-wide investigation in the Japanese population. NHGRI|-1
NM_001173487 NKRF 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2018358 6.49E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001173488 NKRF 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2018358 6.49E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001173531 POU5F1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9501063 2.29E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001173531 POU5F1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9263800 6.55E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001173531 POU5F1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3130931 1.14E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001173531 POU5F1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9263804 1.34E-08 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001173531 POU5F1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113112186 2.97E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001173531 POU5F1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130501 3.87E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001173531 POU5F1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3132524 8.72E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001173539 BANP 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs4843747 2.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_001173539 BANP 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs12447690 6.00E-22 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_001173539 BANP 20485516 http://www.ncbi.nlm.nih.gov/pubmed/20485516 Cornea rs12447690 9.00E-11 Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. NHGRI|-1
NM_001173540 BANP 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs4843747 2.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_001173540 BANP 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs12447690 6.00E-22 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_001173540 BANP 20485516 http://www.ncbi.nlm.nih.gov/pubmed/20485516 Cornea rs12447690 9.00E-11 Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. NHGRI|-1
NM_001173541 BANP 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs4843747 2.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_001173541 BANP 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs12447690 6.00E-22 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_001173541 BANP 20485516 http://www.ncbi.nlm.nih.gov/pubmed/20485516 Cornea rs12447690 9.00E-11 Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. NHGRI|-1
NM_001173542 BANP 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs4843747 2.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_001173542 BANP 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs12447690 6.00E-22 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_001173542 BANP 20485516 http://www.ncbi.nlm.nih.gov/pubmed/20485516 Cornea rs12447690 9.00E-11 Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. NHGRI|-1
NM_001173543 BANP 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs4843747 2.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_001173543 BANP 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs12447690 6.00E-22 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_001173543 BANP 20485516 http://www.ncbi.nlm.nih.gov/pubmed/20485516 Cornea rs12447690 9.00E-11 Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. NHGRI|-1
NM_001173977 LRRC16A 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Iron rs2274089 5.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001173977 LRRC16A 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs2274089 3.00E-07 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001173977 LRRC16A 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs2274089 8.00E-07 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001173977 LRRC16A 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs742132 9.00E-09 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_001173977 LRRC16A 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs932316 9.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001173982 CHST11 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs12811699 8.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_001173984 BRD7 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs8054797 1.11E-08 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001173984 BRD7 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs8044151 6.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001174060 OSBPL10 20610895 http://www.ncbi.nlm.nih.gov/pubmed/20610895 Vascular Diseases rs1902341 5.00E-07 Identification of evidence suggestive of an association with peripheral arterial disease at the OSBPL10 locus by genome-wide investigation in the Japanese population. NHGRI|-1
NM_001174060 OSBPL10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs936160 1.94E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001174069 LMX1A 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs1532815 6.00E-07 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_001174069 LMX1A 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs723821 1.42E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001174087 NCOA3 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs6125048 2.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001174088 NCOA3 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs6125048 2.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001174093 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2839658 1.84E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001174093 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2839658 8.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001174093 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12217563 3.40E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001174093 ZEB1 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001174094 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2839658 1.84E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001174094 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2839658 8.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001174094 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12217563 3.40E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001174094 ZEB1 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001174095 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2839658 1.84E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001174095 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2839658 8.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001174095 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12217563 3.40E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001174095 ZEB1 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001174096 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2839658 1.84E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001174096 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2839658 8.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001174096 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12217563 3.40E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001174096 ZEB1 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001174116 DMXL2 20159242 http://www.ncbi.nlm.nih.gov/pubmed/20159242 Asthma rs17525472 2.00E-06 Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. NHGRI|-1
NM_001174117 DMXL2 20159242 http://www.ncbi.nlm.nih.gov/pubmed/20159242 Asthma rs17525472 2.00E-06 Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. NHGRI|-1
NM_001174146 LMX1B 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs867559 1.00E-07 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001174147 LMX1B 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs867559 1.00E-07 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001174157 ZFAT 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1036819 1.00E-24 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001174157 ZFAT 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs12680655 2.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001174157 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1545240 1.52E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001174157 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs16905215 1.89E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001174157 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs9785140 1.26E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001174158 ZFAT 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1036819 1.00E-24 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001174158 ZFAT 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs12680655 2.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001174158 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1545240 1.52E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001174158 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs16905215 1.89E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001174158 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs9785140 1.26E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001174167 SYK 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic Nephropathies rs773506 6.00E-06 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_001174168 SYK 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic Nephropathies rs773506 6.00E-06 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_001177306 PAM 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs1502844 1.00E-06 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_001177310 TRPM6 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs11144134 8.00E-15 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001177311 TRPM6 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs11144134 8.00E-15 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001177314 RRAS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11023186 9.66E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001177315 RRAS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11023186 9.66E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001177381 CPEB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs16889099 1.85E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001177381 CPEB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2270279 8.13E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001177381 CPEB2 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Count rs10489087 5.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001177381 CPEB2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1013284 4.93E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001177382 CPEB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs16889099 1.85E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001177382 CPEB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2270279 8.13E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001177382 CPEB2 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Count rs10489087 5.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001177382 CPEB2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1013284 4.93E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001177383 CPEB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs16889099 1.85E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001177383 CPEB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2270279 8.13E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001177383 CPEB2 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Count rs10489087 5.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001177383 CPEB2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1013284 4.93E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001177384 CPEB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs16889099 1.85E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001177384 CPEB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2270279 8.13E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001177384 CPEB2 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Count rs10489087 5.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001177384 CPEB2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1013284 4.93E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001177506 AOAH 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs6948404 3.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_001177506 AOAH 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs17329669 9.82E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001177507 AOAH 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs6948404 3.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_001177507 AOAH 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs17329669 9.82E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001177515 BAT5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2295663 8.40E-24 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001177520 ALPL 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs1780324 7.00E-15 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_001177520 ALPL 20558539 http://www.ncbi.nlm.nih.gov/pubmed/20558539 Phosphorus rs1697421 1.00E-27 Common genetic variants associate with serum phosphorus concentration. NHGRI|-1
NM_001177599 SUCLG2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4417811 1.52E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001177608 CD33 18976728 http://www.ncbi.nlm.nih.gov/pubmed/18976728 Alzheimer Disease rs3826656 6.00E-06 Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE. NHGRI|-1
NM_001177608 CD33 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs3865444 2.00E-09 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_001177660 HABP2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4265536 8.64E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001177693 RGNEF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs6869486 4.61E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001177693 RGNEF 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs16871023 1.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001177704 FREM1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs10961780 2.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001177711 RBMS3 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs1530057 3.00E-06 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_001177711 RBMS3 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Bone Density rs10510628 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001177711 RBMS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6778464 1.22E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001177711 RBMS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9877517 6.53E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001177712 RBMS3 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs1530057 3.00E-06 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_001177712 RBMS3 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Bone Density rs10510628 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001177712 RBMS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6778464 1.22E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001177712 RBMS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9877517 6.53E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001177800 ADIPOQ 20018283 http://www.ncbi.nlm.nih.gov/pubmed/20018283 Adiponectin rs17366568 1.00E-41 Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals. NHGRI|-1
NM_001177800 ADIPOQ 19165155 http://www.ncbi.nlm.nih.gov/pubmed/19165155 Adiponectin rs6773957 5.00E-08 Genome-wide linkage and association analyses to identify genes influencing adiponectin levels: the GEMS Study. NHGRI|-1
NM_001177800 ADIPOQ 20011104 http://www.ncbi.nlm.nih.gov/pubmed/20011104 Adiponectin rs266717 9.00E-19 A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. NHGRI|-1
NM_001177800 ADIPOQ 20011104 http://www.ncbi.nlm.nih.gov/pubmed/20011104 Adiponectin rs1648707 3.00E-12 A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. NHGRI|-1
NM_001177800 ADIPOQ 20876611 http://www.ncbi.nlm.nih.gov/pubmed/20876611 Adiponectin rs864265 1.00E-19 Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ. NHGRI|-1
NM_001177875 PCSK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9918149 4.77E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001177876 PCSK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9918149 4.77E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001177969 VIT 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11691187 4.77E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001177970 VIT 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11691187 4.77E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001177971 VIT 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11691187 4.77E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001177972 VIT 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11691187 4.77E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001178 ARNTL 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs900145 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001178002 ATP8B3 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs7250872 2.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_001178003 WDR66 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs7961894 3.00E-44 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001178003 WDR66 19110211 http://www.ncbi.nlm.nih.gov/pubmed/19110211 Platelet Count rs7961894 7.00E-48 A genome-wide association study identifies three loci associated with mean platelet volume. NHGRI|-1
NM_001178003 WDR66 21572414 http://www.ncbi.nlm.nih.gov/pubmed/21572414 Metabolism rs830124 1.00E-46 A genome-wide association study of metabolic traits in human urine. NHGRI|-1
NM_001178004 PCCA 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs681561 9.81E-07 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001178006 SAA1 21124955 http://www.ncbi.nlm.nih.gov/pubmed/21124955 Serum Amyloid A Protein rs4638289 3.00E-53 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. NHGRI|-1
NM_001178008 CBS 20031578 http://www.ncbi.nlm.nih.gov/pubmed/20031578 Homocysteine rs6586282 3.00E-10 "Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study." NHGRI|-1
NM_001178009 CBS 20031578 http://www.ncbi.nlm.nih.gov/pubmed/20031578 Homocysteine rs6586282 3.00E-10 "Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study." NHGRI|-1
NM_001178014 PCCB 20031576 http://www.ncbi.nlm.nih.gov/pubmed/20031576 Fibrinogen rs511154 6.00E-10 Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. NHGRI|-1
NM_001178032 ZC4H2 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs7064929 7.00E-07 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001178032 ZC4H2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7890561 8.45E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001178033 ZC4H2 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs7064929 7.00E-07 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001178033 ZC4H2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7890561 8.45E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001178034 DPP10 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4624391 9.77E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001178034 DPP10 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4277531 9.40E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001178035 C6orf204 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs12210810 2.00E-17 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001178035 C6orf204 19587794 http://www.ncbi.nlm.nih.gov/pubmed/19587794 "Arrhythmias, Cardiac" rs11153730 2.00E-29 Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies. NHGRI|-1
NM_001178035 C6orf204 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11153730 1.00E-18 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001178035 C6orf204 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs11970286 2.00E-24 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001178035 C6orf204 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs11970286 8.00E-07 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001178036 DPP10 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4624391 9.77E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001178036 DPP10 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4277531 9.40E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001178037 DPP10 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4624391 9.77E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001178037 DPP10 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4277531 9.40E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001178044 SLC44A4 20526339 http://www.ncbi.nlm.nih.gov/pubmed/20526339 Vitiligo rs11966200 1.00E-48 Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. NHGRI|-1
NM_001178044 SLC44A4 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs494620 5.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_001178044 SLC44A4 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2736428 1.00E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001178044 SLC44A4 20421499 http://www.ncbi.nlm.nih.gov/pubmed/20421499 Telomere rs2736428 3.00E-06 Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. NHGRI|-1
NM_001178044 SLC44A4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9267658 2.51E-84 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001178045 SLC44A4 20526339 http://www.ncbi.nlm.nih.gov/pubmed/20526339 Vitiligo rs11966200 1.00E-48 Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. NHGRI|-1
NM_001178045 SLC44A4 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs494620 5.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_001178045 SLC44A4 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2736428 1.00E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001178045 SLC44A4 20421499 http://www.ncbi.nlm.nih.gov/pubmed/20421499 Telomere rs2736428 3.00E-06 Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. NHGRI|-1
NM_001178045 SLC44A4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9267658 2.51E-84 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001178055 PARP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13157992 9.03E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001178055 PARP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7720960 7.28E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001178055 PARP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7378969 6.04E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001178055 PARP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1016620 9.80E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001178056 PARP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13157992 9.03E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001178056 PARP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7720960 7.28E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001178056 PARP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7378969 6.04E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001178056 PARP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1016620 9.80E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001178057 ACE 20066004 http://www.ncbi.nlm.nih.gov/pubmed/20066004 Angiotensin-Converting Enzyme Inhibitors rs4343 3.00E-25 A genome-wide association study identifies new loci for ACE activity: potential implications for response to ACE inhibitor. NHGRI|-1
NM_001178063 C2 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs9332739 2.00E-23 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1042663 2.97E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1042663 3.14E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001178063 C2 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs9380272 2.00E-08 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs550605 4.38E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs550605 4.98E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs638383 4.76E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs497239 6.02E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs497239 7.82E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs547154 2.70E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs547154 2.90E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001178063 C2 21105107 http://www.ncbi.nlm.nih.gov/pubmed/21105107 "Carcinoma, Hepatocellular" rs9267673 2.00E-06 Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma. NHGRI|-1
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9267673 2.30E-33 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001178063 C2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs644045 2.06E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs511294 1.45E-13 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs511294 6.27E-13 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs544167 2.48E-13 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001178063 C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs544167 7.79E-13 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001178065 CASR 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs17251221 2.00E-22 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_001178065 CASR 20661308 http://www.ncbi.nlm.nih.gov/pubmed/20661308 Calcium rs1801725 6.00E-37 Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene. NHGRI|-1
NM_001178074 GRIP1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs1082714 5.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_001178078 STAT6 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs167769 2.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_001178079 STAT6 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs167769 2.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_001178080 STAT6 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs167769 2.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_001178081 STAT6 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs167769 2.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_001178091 BCAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10505955 4.33E-04 Genome-wide association between genotype and incident stroke in participants of primarily self-described European ancestry dbGaP|2886
NM_001178092 BCAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10505955 4.33E-04 Genome-wide association between genotype and incident stroke in participants of primarily self-described European ancestry dbGaP|2886
NM_001178093 BCAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10505955 4.33E-04 Genome-wide association between genotype and incident stroke in participants of primarily self-described European ancestry dbGaP|2886
NM_001178094 BCAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10505955 4.33E-04 Genome-wide association between genotype and incident stroke in participants of primarily self-described European ancestry dbGaP|2886
NM_001178096 F3 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs12029080 6.00E-52 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001178097 C12orf74 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10219495 5.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001178100 CD8B 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs6547705 1.00E-08 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_001178117 MINPP1 20304771 http://www.ncbi.nlm.nih.gov/pubmed/20304771 Longevity rs9664222 7.00E-07 A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. NHGRI|-1
NM_001178117 MINPP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12570629 9.12E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001178118 MINPP1 20304771 http://www.ncbi.nlm.nih.gov/pubmed/20304771 Longevity rs9664222 7.00E-07 A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. NHGRI|-1
NM_001178118 MINPP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12570629 9.12E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001178130 EGF 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs9685587 6.63E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001178130 EGF 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs17316633 9.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001178131 EGF 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs9685587 6.63E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001178131 EGF 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs17316633 9.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001178134 CXCL12 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs501120 9.00E-08 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_001178134 CXCL12 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs1746048 3.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001178134 CXCL12 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs1746048 7.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_001178147 CSF3 20172861 http://www.ncbi.nlm.nih.gov/pubmed/20172861 Leukocyte Count rs4794822 6.00E-10 Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count. NHGRI|-1
NM_001178147 CSF3 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs4794822 4.00E-16 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001182 ALDH7A1 20072603 http://www.ncbi.nlm.nih.gov/pubmed/20072603 Osteoporosis rs13182402 2.00E-09 Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis. NHGRI|-1
NM_001184694 MEPE 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1471403 2.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001184694 MEPE 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1471403 8.00E-07 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001184695 MEPE 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1471403 2.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001184695 MEPE 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1471403 8.00E-07 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001184696 MEPE 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1471403 2.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001184696 MEPE 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1471403 8.00E-07 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001184697 MEPE 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1471403 2.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001184697 MEPE 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1471403 8.00E-07 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001184698 MLN 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs2274459 6.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_001184714 SLAMF6 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs16832015 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001184715 SLAMF6 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs16832015 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001184716 SLAMF6 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs16832015 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001184717 TIPARP 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs2665390 3.00E-07 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_001184718 TIPARP 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs2665390 3.00E-07 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_001184734 ASTN2 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs10983238 1.00E-07 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_001184734 ASTN2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs3761845 8.63E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001184734 ASTN2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10817974 1.11E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001184734 ASTN2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs4838255 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001184734 ASTN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs17302884 5.16E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001184735 ASTN2 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs10983238 1.00E-07 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_001184735 ASTN2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs3761845 8.63E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001184735 ASTN2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10817974 1.11E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001184735 ASTN2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs4838255 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001184735 ASTN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs17302884 5.16E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001184743 PGBD1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs13211507 6.73E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001184743 PGBD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs13211507 8.18E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001184746 PAFAH1B2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 "Receptors, Transferrin" rs7112513 6.00E-09 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001184746 PAFAH1B2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs12269901 2.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001184747 PAFAH1B2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 "Receptors, Transferrin" rs7112513 6.00E-09 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001184747 PAFAH1B2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs12269901 2.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001184748 PAFAH1B2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 "Receptors, Transferrin" rs7112513 6.00E-09 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001184748 PAFAH1B2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs12269901 2.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001184751 ZNF408 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7932354 4.00E-09 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001184773 SEZ6L 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Coronary Disease rs688034 4.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001184773 SEZ6L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs667577 8.58E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001184773 SEZ6L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2049988 1.28E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001184774 SEZ6L 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Coronary Disease rs688034 4.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001184774 SEZ6L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs667577 8.58E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001184774 SEZ6L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2049988 1.28E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001184775 SEZ6L 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Coronary Disease rs688034 4.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001184775 SEZ6L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs667577 8.58E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001184775 SEZ6L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2049988 1.28E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001184776 SEZ6L 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Coronary Disease rs688034 4.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001184776 SEZ6L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs667577 8.58E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001184776 SEZ6L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2049988 1.28E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001184777 SEZ6L 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Coronary Disease rs688034 4.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001184777 SEZ6L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs667577 8.58E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001184777 SEZ6L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2049988 1.28E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001184785 PARD3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs563507 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001184785 PARD3 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs7905537 8.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_001184785 PARD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1780436 2.41E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001184785 PARD3 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1780436 3.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001184786 PARD3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs563507 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001184786 PARD3 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs7905537 8.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_001184786 PARD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1780436 2.41E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001184786 PARD3 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1780436 3.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001184787 PARD3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs563507 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001184787 PARD3 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs7905537 8.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_001184787 PARD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1780436 2.41E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001184787 PARD3 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1780436 3.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001184788 PARD3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs563507 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001184788 PARD3 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs7905537 8.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_001184788 PARD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1780436 2.41E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001184788 PARD3 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1780436 3.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001184789 PARD3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs563507 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001184789 PARD3 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs7905537 8.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_001184789 PARD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1780436 2.41E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001184789 PARD3 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1780436 3.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001184790 PARD3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs563507 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001184790 PARD3 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs7905537 8.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_001184790 PARD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1780436 2.41E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001184790 PARD3 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1780436 3.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001184791 PARD3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs563507 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001184791 PARD3 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs7905537 8.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_001184791 PARD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1780436 2.41E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001184791 PARD3 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1780436 3.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001184792 PARD3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs563507 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001184792 PARD3 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs7905537 8.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_001184792 PARD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1780436 2.41E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001184792 PARD3 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1780436 3.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001184793 PARD3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs563507 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001184793 PARD3 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs7905537 8.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_001184793 PARD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1780436 2.41E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001184793 PARD3 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1780436 3.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001184794 PARD3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs563507 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001184794 PARD3 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs7905537 8.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_001184794 PARD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1780436 2.41E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001184794 PARD3 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1780436 3.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001184824 PRMT7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs8058517 4.37E-08 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_001184824 PRMT7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs8058517 8.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001184824 PRMT7 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs7197653 2.00E-06 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001184833 GPR64 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs5955711 9.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001184834 GPR64 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs5955711 9.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001184835 GPR64 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs5955711 9.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001184836 GPR64 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs5955711 9.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001184837 GPR64 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs5955711 9.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001184866 FCRLA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1538972 7.81E-05 NBL-GWAS version 2 dbGaP|2895
NM_001184867 FCRLA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1538972 7.81E-05 NBL-GWAS version 2 dbGaP|2895
NM_001184870 FCRLA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1538972 7.81E-05 NBL-GWAS version 2 dbGaP|2895
NM_001184871 FCRLA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1538972 7.81E-05 NBL-GWAS version 2 dbGaP|2895
NM_001184872 FCRLA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1538972 7.81E-05 NBL-GWAS version 2 dbGaP|2895
NM_001184873 FCRLA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1538972 7.81E-05 NBL-GWAS version 2 dbGaP|2895
NM_001184880 PCDH19 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs5921594 3.79E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001184883 PLCB3 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs2244621 5.00E-10 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001184896 PHF8 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs7065696 4.00E-07 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_001184897 PHF8 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs7065696 4.00E-07 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_001184898 PHF8 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs7065696 4.00E-07 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_001184906 FBXL20 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs7208487 8.00E-07 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001184957 C3orf20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7651825 2.20E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001184958 C3orf20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7651825 2.20E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001184960 SH3KBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs16997315 4.66E-11 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001184963 FXYD4 20598377 http://www.ncbi.nlm.nih.gov/pubmed/20598377 Multiple Sclerosis rs2503875 2.00E-07 Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. NHGRI|-1
NM_001184967 MITF 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs922948 2.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001184968 MITF 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs922948 2.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001184977 UQCC 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs6060369 1.00E-16 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001184977 UQCC 18193045 http://www.ncbi.nlm.nih.gov/pubmed/18193045 Body Height rs6060369 2.00E-16 Common variants in the GDF5-UQCC region are associated with variation in human height. NHGRI|-1
NM_001184977 UQCC 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs6088792 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001184977 UQCC 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs6060373 2.00E-17 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001184977 UQCC 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs6088813 1.00E-13 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001184985 WNK1 19369658 http://www.ncbi.nlm.nih.gov/pubmed/19369658 Stroke rs12425791 1.00E-09 Genomewide association studies of stroke. NHGRI|-1
NM_001184993 RNF17 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1158061 2.59E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001184993 RNF17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9511451 6.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001184993 RNF17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9511479 8.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001184993 RNF17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7335910 2.69E-06 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001185024 ZDHHC8 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs613930 8.67E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001185056 CLDN11 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs6444931 6.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001185056 CLDN11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6444931 1.96E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001185085 ATP12A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2862909 1.03E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001185099 CD22 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4805119 7.57E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001185100 CD22 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4805119 7.57E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001185101 CD22 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4805119 7.57E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001185107 CD1E 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1065457 6.43E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001185108 CD1E 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1065457 6.43E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001185110 CD1E 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1065457 6.43E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001185112 CD1E 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1065457 6.43E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001185113 CD1E 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1065457 6.43E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001185114 CD1E 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1065457 6.43E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001185115 CD1E 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1065457 6.43E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001185118 MYNN 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs10936599 5.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001185118 MYNN 20972440 http://www.ncbi.nlm.nih.gov/pubmed/20972440 Colorectal Neoplasms rs10936599 3.00E-08 "Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33." NHGRI|-1
NM_001185119 MYNN 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs10936599 5.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001185119 MYNN 20972440 http://www.ncbi.nlm.nih.gov/pubmed/20972440 Colorectal Neoplasms rs10936599 3.00E-08 "Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33." NHGRI|-1
NM_001188 BAK1 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs210135 4.00E-10 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001188 BAK1 19483681 http://www.ncbi.nlm.nih.gov/pubmed/19483681 Testicular Neoplasms rs210138 1.00E-13 A genome-wide association study of testicular germ cell tumor. NHGRI|-1
NM_001188 BAK1 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs9394152 7.00E-08 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001188 BAK1 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs9296092 6.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_001190241 IFT80 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6441306 3.52E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001190242 IFT80 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6441306 3.52E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001190263 C1D 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs724568 5.00E-06 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_001190265 C1D 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs724568 5.00E-06 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_001190266 ATG16L1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs10210302 5.00E-14 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001190266 ATG16L1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs3828309 2.00E-32 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001190266 ATG16L1 17435756 http://www.ncbi.nlm.nih.gov/pubmed/17435756 Crohn Disease rs2241880 1.00E-13 Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. NHGRI|-1
NM_001190266 ATG16L1 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs2241880 3.00E-06 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_001190266 ATG16L1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2241880 4.40E-08 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001190266 ATG16L1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs3792109 7.00E-41 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001190266 ATG16L1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs3792106 2.31E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001190266 ATG16L1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs10933436 7.00E-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001190267 ATG16L1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs10210302 5.00E-14 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001190267 ATG16L1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs3828309 2.00E-32 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001190267 ATG16L1 17435756 http://www.ncbi.nlm.nih.gov/pubmed/17435756 Crohn Disease rs2241880 1.00E-13 Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. NHGRI|-1
NM_001190267 ATG16L1 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs2241880 3.00E-06 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_001190267 ATG16L1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2241880 4.40E-08 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001190267 ATG16L1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs3792109 7.00E-41 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001190267 ATG16L1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs3792106 2.31E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001190267 ATG16L1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs10933436 7.00E-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001190411 RPH3AL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11869174 1.23E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001190411 RPH3AL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4247113 2.62E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001190411 RPH3AL 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4130140 2.30E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001190411 RPH3AL 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs7217319 4.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_001190412 RPH3AL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11869174 1.23E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001190412 RPH3AL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4247113 2.62E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001190412 RPH3AL 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4130140 2.30E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001190412 RPH3AL 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs7217319 4.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_001190413 RPH3AL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11869174 1.23E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001190413 RPH3AL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4247113 2.62E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001190413 RPH3AL 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4130140 2.30E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001190413 RPH3AL 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs7217319 4.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_001190442 CAST 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4434401 6.76E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001190442 CAST 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10053056 2.19E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001190442 CAST 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs27524 3.00E-11 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_001190442 CAST 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9918149 4.77E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001190447 PPP2R3A 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs823968 6.68E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001190455 CHRNA7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4779984 1.58E-05 NBL-GWAS version 2 dbGaP|2895
NM_001190455 CHRNA7 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1001555 3.75E-06 NBL-GWAS version 1 dbGaP|2845
NM_001190456 CORO2B 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs8030672 1.00E-11 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001190456 CORO2B 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs1445021 9.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001190456 CORO2B 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs11856323 1.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001190457 CORO2B 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs8030672 1.00E-11 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001190457 CORO2B 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs1445021 9.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001190457 CORO2B 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs11856323 1.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001190463 CTH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001190463 CTH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 8.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001190463 CTH 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs10458561 4.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NM_001190468 GDNF 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs270545 1.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_001190469 GDNF 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs270545 1.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_001190481 CLSPN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs577483 3.31E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001190481 CLSPN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs535638 3.92E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001190482 PCSK5 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs10512049 3.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001190482 PCSK5 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs12344488 5.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001190482 PCSK5 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2842483 5.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001190489 MTRNR2L7 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs7474896 9.00E-07 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_001190489 MTRNR2L7 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Indices rs1200821 6.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001190707 ALS2CL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs7633016 3.19E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001190707 ALS2CL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4076927 2.53E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001190709 COL11A1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1415363 5.62E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001190709 COL11A1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Fibrinogen rs10874639 3.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001190716 DNM2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11671653 9.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001190727 C9orf103 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10868025 1.79E-07 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001190727 C9orf103 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10868025 6.46E-07 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001190737 NFIB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10435726 4.14E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001190737 NFIB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10435726 6.42E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001190738 NFIB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10435726 4.14E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001190738 NFIB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10435726 6.42E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001190807 CYB5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10514115 6.18E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001190821 SMAD7 17934461 http://www.ncbi.nlm.nih.gov/pubmed/17934461 Colorectal Neoplasms rs4939827 1.00E-12 A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. NHGRI|-1
NM_001190821 SMAD7 18372905 http://www.ncbi.nlm.nih.gov/pubmed/18372905 Colorectal Neoplasms rs4939827 2.00E-06 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. NHGRI|-1
NM_001190821 SMAD7 18372901 http://www.ncbi.nlm.nih.gov/pubmed/18372901 Colorectal Neoplasms rs4939827 8.00E-28 Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. NHGRI|-1
NM_001190822 SMAD7 17934461 http://www.ncbi.nlm.nih.gov/pubmed/17934461 Colorectal Neoplasms rs4939827 1.00E-12 A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. NHGRI|-1
NM_001190822 SMAD7 18372905 http://www.ncbi.nlm.nih.gov/pubmed/18372905 Colorectal Neoplasms rs4939827 2.00E-06 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. NHGRI|-1
NM_001190822 SMAD7 18372901 http://www.ncbi.nlm.nih.gov/pubmed/18372901 Colorectal Neoplasms rs4939827 8.00E-28 Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. NHGRI|-1
NM_001190823 SMAD7 17934461 http://www.ncbi.nlm.nih.gov/pubmed/17934461 Colorectal Neoplasms rs4939827 1.00E-12 A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. NHGRI|-1
NM_001190823 SMAD7 18372905 http://www.ncbi.nlm.nih.gov/pubmed/18372905 Colorectal Neoplasms rs4939827 2.00E-06 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. NHGRI|-1
NM_001190823 SMAD7 18372901 http://www.ncbi.nlm.nih.gov/pubmed/18372901 Colorectal Neoplasms rs4939827 8.00E-28 Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. NHGRI|-1
NM_001190880 HYI 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12069733 8.59E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001190892 PDYN 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs6136489 8.00E-11 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001190892 PDYN 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs6045676 3.00E-08 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_001190898 PDYN 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs6136489 8.00E-11 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001190898 PDYN 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs6045676 3.00E-08 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_001190899 PDYN 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs6136489 8.00E-11 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001190899 PDYN 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs6045676 3.00E-08 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_001190900 PDYN 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs6136489 8.00E-11 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001190900 PDYN 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs6045676 3.00E-08 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_001190945 TRAF1 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs3761847 2.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001190945 TRAF1 17804836 http://www.ncbi.nlm.nih.gov/pubmed/17804836 "Arthritis, Rheumatoid" rs3761847 4.00E-14 TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. NHGRI|-1
NM_001190945 TRAF1 19503088 http://www.ncbi.nlm.nih.gov/pubmed/19503088 "Arthritis, Rheumatoid" rs881375 4.00E-08 "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis." NHGRI|-1
NM_001190947 TRAF1 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs3761847 2.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001190947 TRAF1 17804836 http://www.ncbi.nlm.nih.gov/pubmed/17804836 "Arthritis, Rheumatoid" rs3761847 4.00E-14 TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. NHGRI|-1
NM_001190947 TRAF1 19503088 http://www.ncbi.nlm.nih.gov/pubmed/19503088 "Arthritis, Rheumatoid" rs881375 4.00E-08 "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis." NHGRI|-1
NM_001190995 IPO8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs2046383 1.97E-04 Genome-wide association between genotype and incident heart failure in African-American participants dbGaP|2885
NM_001190995 IPO8 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs2046383 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_001190995 IPO8 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Aging rs1463605 7.00E-08 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_001190996 ARPC1A 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs740160 2.00E-16 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001190997 SLC6A13 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Creatinine rs10774021 1.00E-09 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001191028 TNPO3 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs12531711 9.00E-17 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001191028 TNPO3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs12531711 2.29E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001191028 TNPO3 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs12531711 6.00E-09 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_001191028 TNPO3 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs10488631 4.00E-11 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001191028 TNPO3 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs10488631 2.00E-07 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_001191028 TNPO3 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs10488631 3.00E-10 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_001191028 TNPO3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 1.65E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001191028 TNPO3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10488631 2.48E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001191028 TNPO3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 2.00E-11 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_001191028 TNPO3 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs10488631 7.00E-18 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_001191028 TNPO3 20383147 http://www.ncbi.nlm.nih.gov/pubmed/20383147 "Scleroderma, Systemic" rs10488631 2.00E-13 Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. NHGRI|-1
NM_001191028 TNPO3 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs10488631 4.00E-07 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_001191035 C8orf83 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs16915399 9.45E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001191035 C8orf83 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6471335 1.33E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001191036 C8orf83 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs16915399 9.45E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001191036 C8orf83 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6471335 1.33E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001191056 PDE1C 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs215614 2.00E-07 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_001191057 PDE1C 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs215614 2.00E-07 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_001191058 PDE1C 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs215614 2.00E-07 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_001191059 PDE1C 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs215614 2.00E-07 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_001191320 GABRB3 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs8043440 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001191320 GABRB3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs3212335 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001191321 GABRB3 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs8043440 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001191321 GABRB3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs3212335 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001191322 GREM1 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs1258763 1.00E-06 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_001191322 GREM1 18372905 http://www.ncbi.nlm.nih.gov/pubmed/18372905 Colorectal Neoplasms rs4779584 5.00E-07 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. NHGRI|-1
NM_001191323 GREM1 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs1258763 1.00E-06 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_001191323 GREM1 18372905 http://www.ncbi.nlm.nih.gov/pubmed/18372905 Colorectal Neoplasms rs4779584 5.00E-07 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. NHGRI|-1
NM_001193277 MID1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs5934953 1.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001193277 MID1 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs12388359 4.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_001193283 LEKR1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs12638253 2.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001193283 LEKR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12638253 8.31E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001193283 LEKR1 20372150 http://www.ncbi.nlm.nih.gov/pubmed/20372150 Birth Weight rs900400 2.00E-35 Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. NHGRI|-1
NM_001193283 LEKR1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs13064954 7.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001193288 SLC24A2 19187332 http://www.ncbi.nlm.nih.gov/pubmed/19187332 Asthma rs16937883 7.00E-06 Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis. NHGRI|-1
NM_001193289 APOBEC3A 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs1014971 8.00E-12 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_001193311 C7orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17527624 1.33E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001193311 C7orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17688601 3.62E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001193311 C7orf10 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs29880 7.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001193311 C7orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11505535 6.37E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001193311 C7orf10 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1079866 6.00E-14 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001193311 C7orf10 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Height rs10486715 3.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001193312 C7orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17527624 1.33E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001193312 C7orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17688601 3.62E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001193312 C7orf10 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs29880 7.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001193312 C7orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11505535 6.37E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001193312 C7orf10 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1079866 6.00E-14 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001193312 C7orf10 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Height rs10486715 3.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001193313 C7orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17527624 1.33E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001193313 C7orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17688601 3.62E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001193313 C7orf10 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs29880 7.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001193313 C7orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11505535 6.37E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001193313 C7orf10 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1079866 6.00E-14 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001193313 C7orf10 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Height rs10486715 3.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001193318 RNF212 18239089 http://www.ncbi.nlm.nih.gov/pubmed/18239089 "Recombination, Genetic" rs1670533 2.00E-12 Sequence variants in the RNF212 gene associate with genome-wide recombination rate. NHGRI|-1
NM_001193318 RNF212 18239089 http://www.ncbi.nlm.nih.gov/pubmed/18239089 "Recombination, Genetic" rs3796619 3.00E-24 Sequence variants in the RNF212 gene associate with genome-wide recombination rate. NHGRI|-1
NM_001193318 RNF212 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6839931 2.09E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001193318 RNF212 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7669622 4.53E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001193318 RNF212 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6827357 5.15E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001193329 C9orf3 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs3802458 4.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001193331 C9orf3 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs3802458 4.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001193334 WLS 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs187922 2.61E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001193334 WLS 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1430742 3.00E-13 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001193334 WLS 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2566755 2.00E-12 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001193347 MEF2C 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs770189 3.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001193347 MEF2C 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs10037512 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001193347 MEF2C 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1366594 1.00E-13 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001193347 MEF2C 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs1366594 1.00E-07 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_001193347 MEF2C 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs1366594 8.00E-10 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_001193347 MEF2C 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs12518099 7.00E-07 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001193347 MEF2C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2972956 6.07E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001193347 MEF2C 21060863 http://www.ncbi.nlm.nih.gov/pubmed/21060863 Retinal Vein rs17421627 7.00E-16 "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo." NHGRI|-1
NM_001193348 MEF2C 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs770189 3.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001193348 MEF2C 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs10037512 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001193348 MEF2C 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1366594 1.00E-13 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001193348 MEF2C 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs1366594 1.00E-07 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_001193348 MEF2C 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs1366594 8.00E-10 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_001193348 MEF2C 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs12518099 7.00E-07 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001193348 MEF2C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2972956 6.07E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001193348 MEF2C 21060863 http://www.ncbi.nlm.nih.gov/pubmed/21060863 Retinal Vein rs17421627 7.00E-16 "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo." NHGRI|-1
NM_001193350 MEF2C 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs770189 3.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001193350 MEF2C 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs10037512 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001193350 MEF2C 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1366594 1.00E-13 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001193350 MEF2C 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs1366594 1.00E-07 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_001193350 MEF2C 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs1366594 8.00E-10 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_001193350 MEF2C 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs12518099 7.00E-07 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001193350 MEF2C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2972956 6.07E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001193350 MEF2C 21060863 http://www.ncbi.nlm.nih.gov/pubmed/21060863 Retinal Vein rs17421627 7.00E-16 "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo." NHGRI|-1
NM_001193360 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 2.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001193360 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001193361 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 2.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001193361 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001193362 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 2.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001193362 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001193363 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 2.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001193363 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001193376 TERT 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Count rs2736100 3.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001193376 TERT 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs2736100 1.00E-14 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_001193376 TERT 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs2736100 2.00E-17 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_001193376 TERT 18835860 http://www.ncbi.nlm.nih.gov/pubmed/18835860 Idiopathic Pulmonary Fibrosis rs2736100 3.00E-08 A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis. NHGRI|-1
NM_001193376 TERT 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs2736100 1.00E-27 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_001193376 TERT 19836008 http://www.ncbi.nlm.nih.gov/pubmed/19836008 Lung Neoplasms rs2736100 2.00E-10 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. NHGRI|-1
NM_001193376 TERT 20700438 http://www.ncbi.nlm.nih.gov/pubmed/20700438 Lung Neoplasms rs2736100 2.00E-22 The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia. NHGRI|-1
NM_001193376 TERT 20871597 http://www.ncbi.nlm.nih.gov/pubmed/20871597 Lung Neoplasms rs2736100 3.00E-11 Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations. NHGRI|-1
NM_001193376 TERT 20543847 http://www.ncbi.nlm.nih.gov/pubmed/20543847 Testicular Neoplasms rs2736100 8.00E-15 "Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer." NHGRI|-1
NM_001193376 TERT 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs2853676 4.00E-14 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_001193376 TERT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4635969 1.05E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001193376 TERT 20543847 http://www.ncbi.nlm.nih.gov/pubmed/20543847 Testicular Neoplasms rs4635969 1.00E-23 "Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer." NHGRI|-1
NM_001193376 TERT 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs4975616 3.00E-09 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_001193376 TERT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4975616 8.29E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001193431 PTPN22 17804836 http://www.ncbi.nlm.nih.gov/pubmed/17804836 "Arthritis, Rheumatoid" rs2476601 2.00E-11 TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. NHGRI|-1
NM_001193431 PTPN22 19503088 http://www.ncbi.nlm.nih.gov/pubmed/19503088 "Arthritis, Rheumatoid" rs2476601 2.00E-21 "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis." NHGRI|-1
NM_001193431 PTPN22 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs2476601 9.00E-74 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001193431 PTPN22 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2476601 1.00E-08 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001193431 PTPN22 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 "Diabetes Mellitus, Type 1" rs2476601 1.00E-07 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NM_001193431 PTPN22 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs2476601 2.00E-80 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_001193431 PTPN22 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2476601 9.00E-85 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001193431 PTPN22 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs2476601 1.00E-07 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_001193455 NSUN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs563624 6.12E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001193460 MSRB3 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs10506525 6.00E-09 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001193460 MSRB3 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs10506525 9.00E-07 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001193460 MSRB3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10784460 2.18E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001193460 MSRB3 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic Nephropathies rs2358944 4.00E-06 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_001193461 MSRB3 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs10506525 6.00E-09 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001193461 MSRB3 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs10506525 9.00E-07 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001193461 MSRB3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10784460 2.18E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001193461 MSRB3 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic Nephropathies rs2358944 4.00E-06 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_001193465 KIAA1267 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2532274 2.22E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001193465 KIAA1267 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2532269 2.70E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001193465 KIAA1267 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2668692 3.94E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001193466 KIAA1267 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2532274 2.22E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001193466 KIAA1267 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2532269 2.70E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001193466 KIAA1267 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2668692 3.94E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001193471 FOLH1B 20801717 http://www.ncbi.nlm.nih.gov/pubmed/20801717 Amyotrophic Lateral Sclerosis rs1488902 3.00E-06 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. NHGRI|-1
NM_001193472 FOLH1B 20801717 http://www.ncbi.nlm.nih.gov/pubmed/20801717 Amyotrophic Lateral Sclerosis rs1488902 3.00E-06 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. NHGRI|-1
NM_001193473 FOLH1B 20801717 http://www.ncbi.nlm.nih.gov/pubmed/20801717 Amyotrophic Lateral Sclerosis rs1488902 3.00E-06 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. NHGRI|-1
NM_001193508 REST 21106707 http://www.ncbi.nlm.nih.gov/pubmed/21106707 Bleomycin rs708547 9.00E-07 A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity. NHGRI|-1
NM_001193520 RASAL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7976407 7.44E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001193521 RASAL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7976407 7.44E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001193544 ANXA6 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs17728338 1.00E-20 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NM_001193582 NRCAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs409797 8.78E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001193583 NRCAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs409797 8.78E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001193584 NRCAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs409797 8.78E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001193640 CRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10754220 2.85E-10 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001193640 CRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10754220 4.20E-11 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001193640 CRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1415214 9.74E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001193640 CRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs949571 3.31E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001193640 CRB1 20032318 http://www.ncbi.nlm.nih.gov/pubmed/20032318 Asthma rs2786098 2.00E-13 Variants of DENND1B associated with asthma in children. NHGRI|-1
NM_001193640 CRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1764629 5.01E-06 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001193653 C17orf62 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Insulin-Like Growth Factor I rs9303029 4.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001193654 C17orf62 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Insulin-Like Growth Factor I rs9303029 4.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001193655 C17orf62 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Insulin-Like Growth Factor I rs9303029 4.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001193657 C17orf62 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Insulin-Like Growth Factor I rs9303029 4.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001194997 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs729662 8.52E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001194997 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7481584 9.54E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001194997 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001194997 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 4.55E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001194997 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 7.54E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001194997 CARS 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs739401 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001194997 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs438384 1.07E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001194997 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 2.60E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001194997 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 3.06E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001194997 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 9.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001194997 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs369461 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001194997 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs369461 7.87E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001194998 CEP152 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs17463995 4.89E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001195001 PTPRU 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1932397 7.14E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001195001 PTPRU 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9286938 9.14E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001195001 PTPRU 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs4949526 4.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001195001 PTPRU 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11580589 2.48E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001195001 PTPRU 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs910696 3.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001195001 PTPRU 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs2180233 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001195010 GRHL3 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs4649203 7.00E-08 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_001195032 C6orf99 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9365009 4.19E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_001195044 YAP1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs2852894 1.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001195045 YAP1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs2852894 1.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001195059 PLEKHO2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs12595292 9.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001195106 TLR10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6838905 6.46E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001195106 TLR10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6838905 7.66E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001195106 TLR10 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7658334 1.49E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001195107 TLR10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6838905 6.46E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001195107 TLR10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6838905 7.66E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001195107 TLR10 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7658334 1.49E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001195108 TLR10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6838905 6.46E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001195108 TLR10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6838905 7.66E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001195108 TLR10 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7658334 1.49E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001195215 DENND1B 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs1998598 9.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001195216 DENND1B 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs1998598 9.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001195248 APTX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10971259 1.34E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001195249 APTX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10971259 1.34E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001195250 APTX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10971259 1.34E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001195251 APTX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10971259 1.34E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001195252 APTX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10971259 1.34E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001195254 APTX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10971259 1.34E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001195263 PDZD7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs701837 1.19E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001195286 IRF4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs12203592 2.00E-15 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001195286 IRF4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12203592 2.00E-28 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001195286 IRF4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12203592 4.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001195286 IRF4 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs12203592 7.00E-127 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_001195286 IRF4 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs12203592 9.00E-28 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_001195286 IRF4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Melanosis rs12203592 2.00E-91 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001195286 IRF4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12203592 4.90E-05 NBL-GWAS version 2 dbGaP|2895
NM_001195286 IRF4 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs12203592 6.00E-15 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_001195286 IRF4 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs872071 2.00E-20 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NM_001195286 IRF4 21131588 http://www.ncbi.nlm.nih.gov/pubmed/21131588 "Leukemia, Lymphoid" rs9378805 2.00E-06 Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL. NHGRI|-1
NM_001195286 IRF4 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Melanosis rs1540771 4.00E-18 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_001195286 IRF4 21700618 http://www.ncbi.nlm.nih.gov/pubmed/21700618 "Carcinoma, Basal Cell" rs12210050 1.00E-09 Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma. NHGRI|-1
NM_001195286 IRF4 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs12210050 5.00E-14 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_001195286 IRF4 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1033180 6.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001195303 RGS5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4657247 1.05E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001195303 RGS5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12566267 8.82E-06 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001195303 RGS5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4132246 4.90E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001195381 GPR35 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs4676406 8.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001195382 GPR35 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs4676406 8.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001195388 FCRL5 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs6427356 8.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001195396 ARL4A 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs732577 4.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001195415 DCLK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1539549 2.28E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001195415 DCLK1 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1926320 1.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_001195415 DCLK1 17903306 http://www.ncbi.nlm.nih.gov/pubmed/17903306 Heart Rate rs9315385 8.00E-06 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. NHGRI|-1
NM_001195416 DCLK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1539549 2.28E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001195416 DCLK1 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1926320 1.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_001195416 DCLK1 17903306 http://www.ncbi.nlm.nih.gov/pubmed/17903306 Heart Rate rs9315385 8.00E-06 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. NHGRI|-1
NM_001195430 DCLK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1539549 2.28E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001195430 DCLK1 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1926320 1.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_001195430 DCLK1 17903306 http://www.ncbi.nlm.nih.gov/pubmed/17903306 Heart Rate rs9315385 8.00E-06 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. NHGRI|-1
NM_001195432 MLF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1714524 1.36E-05 NBL-GWAS version 2 dbGaP|2895
NM_001195432 MLF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1656377 4.94E-05 NBL-GWAS version 2 dbGaP|2895
NM_001195433 MLF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1714524 1.36E-05 NBL-GWAS version 2 dbGaP|2895
NM_001195433 MLF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1656377 4.94E-05 NBL-GWAS version 2 dbGaP|2895
NM_001195434 MLF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1714524 1.36E-05 NBL-GWAS version 2 dbGaP|2895
NM_001195434 MLF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1656377 4.94E-05 NBL-GWAS version 2 dbGaP|2895
NM_001195470 SATB1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs6792314 8.60E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001195470 SATB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11914608 1.42E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001195470 SATB1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs13073817 7.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001195470 SATB1 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs6809854 1.00E-07 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_001195536 CHMP5 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs12336160 1.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_001195573 DICER1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11624318 7.62E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001195573 DICER1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11160219 3.45E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001195573 DICER1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8007115 4.06E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001195573 DICER1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs8019257 8.50E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751890 1.61E-15 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751890 2.15E-16 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001195608 PLEKHA1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs6585827 2.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6585827 1.12E-21 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6585827 1.42E-23 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2280141 1.06E-21 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2280141 1.37E-23 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2292627 2.68E-17 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2292627 4.68E-18 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1882907 4.02E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1882907 6.27E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7091160 1.81E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6585818 1.92E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11598094 2.21E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11598094 5.64E-07 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7080960 4.24E-11 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7080960 5.76E-12 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11200583 5.76E-16 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11200583 8.67E-16 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751889 1.73E-14 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001195608 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751889 2.26E-15 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001195610 DCDC2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs793834 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_001195641 PLA2R1 21323541 http://www.ncbi.nlm.nih.gov/pubmed/21323541 "Glomerulonephritis, Membranous" rs4664308 9.00E-29 Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy. NHGRI|-1
NM_001195653 ZGPAT 18758464 http://www.ncbi.nlm.nih.gov/pubmed/18758464 Inflammatory Bowel Diseases rs2315008 9.00E-15 Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. NHGRI|-1
NM_001195653 ZGPAT 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs4809330 3.00E-15 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001195654 ZGPAT 18758464 http://www.ncbi.nlm.nih.gov/pubmed/18758464 Inflammatory Bowel Diseases rs2315008 9.00E-15 Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. NHGRI|-1
NM_001195654 ZGPAT 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs4809330 3.00E-15 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001195683 TGFBR3 19249006 http://www.ncbi.nlm.nih.gov/pubmed/19249006 Bone Density rs17131547 1.00E-06 Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups. NHGRI|-1
NM_001195684 TGFBR3 19249006 http://www.ncbi.nlm.nih.gov/pubmed/19249006 Bone Density rs17131547 1.00E-06 Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups. NHGRI|-1
NM_001195736 C1orf93 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs734999 3.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001195737 C1orf93 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs734999 3.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001195738 C1orf93 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs734999 3.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001195740 C1orf93 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs734999 3.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001195741 C1orf93 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs734999 3.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001195798 LDLR 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs6511720 2.00E-26 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001195798 LDLR 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs6511720 2.00E-51 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_001195798 LDLR 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs6511720 4.00E-26 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001195798 LDLR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs2228671 4.00E-14 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001195798 LDLR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs2228671 9.00E-24 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001195798 LDLR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs2228671 2.34E-06 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001195798 LDLR 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs2738459 7.00E-06 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001195798 LDLR 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs11668477 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001195798 LDLR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs11668477 1.51E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001195799 LDLR 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs6511720 2.00E-26 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001195799 LDLR 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs6511720 2.00E-51 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_001195799 LDLR 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs6511720 4.00E-26 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001195799 LDLR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs2228671 4.00E-14 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001195799 LDLR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs2228671 9.00E-24 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001195799 LDLR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs2228671 2.34E-06 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001195799 LDLR 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs2738459 7.00E-06 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001195799 LDLR 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs11668477 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001195799 LDLR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs11668477 1.51E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001195800 LDLR 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs6511720 2.00E-26 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001195800 LDLR 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs6511720 2.00E-51 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_001195800 LDLR 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs6511720 4.00E-26 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001195800 LDLR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs2228671 4.00E-14 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001195800 LDLR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs2228671 9.00E-24 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001195800 LDLR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs2228671 2.34E-06 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001195800 LDLR 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs2738459 7.00E-06 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001195800 LDLR 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs11668477 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001195800 LDLR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs11668477 1.51E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001195802 LDLR 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs6511720 2.00E-26 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001195802 LDLR 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs6511720 2.00E-51 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_001195802 LDLR 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs6511720 4.00E-26 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001195802 LDLR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs2228671 4.00E-14 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001195802 LDLR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs2228671 9.00E-24 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001195802 LDLR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs2228671 2.34E-06 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001195802 LDLR 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs2738459 7.00E-06 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001195802 LDLR 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs11668477 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001195802 LDLR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs11668477 1.51E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001195803 LDLR 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs6511720 2.00E-26 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001195803 LDLR 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs6511720 2.00E-51 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_001195803 LDLR 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs6511720 4.00E-26 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001195803 LDLR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs2228671 4.00E-14 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001195803 LDLR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs2228671 9.00E-24 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001195803 LDLR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs2228671 2.34E-06 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001195803 LDLR 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs2738459 7.00E-06 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001195803 LDLR 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs11668477 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001195803 LDLR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs11668477 1.51E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001197 BIK 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs742134 6.00E-06 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_001197 BIK 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs5759167 1.00E-05 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_001197 BIK 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs5759167 6.00E-29 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001197020 PRSS55 20452100 http://www.ncbi.nlm.nih.gov/pubmed/20452100 Neurofibrillary Tangles rs11782819 3.00E-06 Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study. NHGRI|-1
NM_001197079 IFRD1 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs17159640 9.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_001197080 IFRD1 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs17159640 9.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_001197097 PRSS3 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs216345 4.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001197098 PRSS3 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs216345 4.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001197107 SCHIP1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Waist Circumference rs2222328 8.00E-07 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001197108 SCHIP1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Waist Circumference rs2222328 8.00E-07 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001197109 SCHIP1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Waist Circumference rs2222328 8.00E-07 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001197113 SCHIP1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Waist Circumference rs2222328 8.00E-07 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001197114 SCHIP1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Waist Circumference rs2222328 8.00E-07 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001197129 SYS1 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs1008953 1.00E-07 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_001197218 PDE4D 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs10052657 2.00E-19 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001197218 PDE4D 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs1823068 3.00E-08 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_001197218 PDE4D 17667963 http://www.ncbi.nlm.nih.gov/pubmed/17667963 Neurotic Disorders rs702543 2.00E-06 A whole genome association study of neuroticism using DNA pooling. NHGRI|-1
NM_001197218 PDE4D 19426955 http://www.ncbi.nlm.nih.gov/pubmed/19426955 Asthma rs1588265 3.00E-08 Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. NHGRI|-1
NM_001197219 PDE4D 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs10052657 2.00E-19 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001197219 PDE4D 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs1823068 3.00E-08 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_001197219 PDE4D 17667963 http://www.ncbi.nlm.nih.gov/pubmed/17667963 Neurotic Disorders rs702543 2.00E-06 A whole genome association study of neuroticism using DNA pooling. NHGRI|-1
NM_001197219 PDE4D 19426955 http://www.ncbi.nlm.nih.gov/pubmed/19426955 Asthma rs1588265 3.00E-08 Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. NHGRI|-1
NM_001197220 PDE4D 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs10052657 2.00E-19 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001197220 PDE4D 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs1823068 3.00E-08 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_001197220 PDE4D 17667963 http://www.ncbi.nlm.nih.gov/pubmed/17667963 Neurotic Disorders rs702543 2.00E-06 A whole genome association study of neuroticism using DNA pooling. NHGRI|-1
NM_001197220 PDE4D 19426955 http://www.ncbi.nlm.nih.gov/pubmed/19426955 Asthma rs1588265 3.00E-08 Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. NHGRI|-1
NM_001197221 PDE4D 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs10052657 2.00E-19 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001197221 PDE4D 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs1823068 3.00E-08 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_001197221 PDE4D 17667963 http://www.ncbi.nlm.nih.gov/pubmed/17667963 Neurotic Disorders rs702543 2.00E-06 A whole genome association study of neuroticism using DNA pooling. NHGRI|-1
NM_001197221 PDE4D 19426955 http://www.ncbi.nlm.nih.gov/pubmed/19426955 Asthma rs1588265 3.00E-08 Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. NHGRI|-1
NM_001197222 PDE4D 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs10052657 2.00E-19 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001197222 PDE4D 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs1823068 3.00E-08 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_001197222 PDE4D 17667963 http://www.ncbi.nlm.nih.gov/pubmed/17667963 Neurotic Disorders rs702543 2.00E-06 A whole genome association study of neuroticism using DNA pooling. NHGRI|-1
NM_001197222 PDE4D 19426955 http://www.ncbi.nlm.nih.gov/pubmed/19426955 Asthma rs1588265 3.00E-08 Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. NHGRI|-1
NM_001197223 PDE4D 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs10052657 2.00E-19 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001197223 PDE4D 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs1823068 3.00E-08 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_001197223 PDE4D 17667963 http://www.ncbi.nlm.nih.gov/pubmed/17667963 Neurotic Disorders rs702543 2.00E-06 A whole genome association study of neuroticism using DNA pooling. NHGRI|-1
NM_001197223 PDE4D 19426955 http://www.ncbi.nlm.nih.gov/pubmed/19426955 Asthma rs1588265 3.00E-08 Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. NHGRI|-1
NM_001197233 BTN2A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs13195509 1.17E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197233 BTN2A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs13195509 7.66E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001197233 BTN2A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9358946 1.12E-08 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197233 BTN2A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs16891725 6.05E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197234 BTN2A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs13195509 1.17E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197234 BTN2A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs13195509 7.66E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001197234 BTN2A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9358946 1.12E-08 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197234 BTN2A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs16891725 6.05E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197244 BCL7B 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs13233571 4.00E-09 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001197246 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9379858 6.21E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197246 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9379859 3.79E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197246 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs12176317 6.83E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197247 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9379858 6.21E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197247 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9379859 3.79E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197247 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs12176317 6.83E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197248 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9379858 6.21E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197248 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9379859 3.79E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197248 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs12176317 6.83E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197249 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9379858 6.21E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197249 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9379859 3.79E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197249 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs12176317 6.83E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001197317 CLEC2D 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs3764021 5.00E-08 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001197318 CLEC2D 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs3764021 5.00E-08 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001197319 CLEC2D 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs3764021 5.00E-08 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001198 PRDM1 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs548234 5.00E-12 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_001198 PRDM1 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs9386463 6.00E-07 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001198 PRDM1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs7746082 2.00E-10 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001198 PRDM1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6911490 1.00E-08 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001198525 TCF7L2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7901695 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001198525 TCF7L2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs7901695 1.00E-48 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001198525 TCF7L2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs4506565 5.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001198525 TCF7L2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4506565 1.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001198525 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.25E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001198525 TCF7L2 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs7903146 1.00E-30 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001198525 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001198525 TCF7L2 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs7903146 2.00E-10 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001198525 TCF7L2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs7903146 2.00E-31 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001198525 TCF7L2 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs7903146 2.00E-34 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001198525 TCF7L2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7903146 2.00E-51 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001198525 TCF7L2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7903146 3.00E-23 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001198525 TCF7L2 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs7903146 5.00E-08 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_001198525 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 6.00E-16 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001198525 TCF7L2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs7903146 7.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001198525 TCF7L2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs7903146 8.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001198525 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 9.00E-30 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001198525 TCF7L2 20849430 http://www.ncbi.nlm.nih.gov/pubmed/20849430 "Hemoglobin A, Glycosylated" rs7903146 1.00E-07 The TCF7L2 diabetes risk variant is associated with HbAG??(C) levels: a genome-wide association meta-analysis. NHGRI|-1
NM_001198525 TCF7L2 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs12243326 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001198525 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12255372 1.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001198526 TCF7L2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7901695 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001198526 TCF7L2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs7901695 1.00E-48 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001198526 TCF7L2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs4506565 5.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001198526 TCF7L2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4506565 1.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001198526 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.25E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001198526 TCF7L2 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs7903146 1.00E-30 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001198526 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001198526 TCF7L2 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs7903146 2.00E-10 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001198526 TCF7L2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs7903146 2.00E-31 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001198526 TCF7L2 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs7903146 2.00E-34 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001198526 TCF7L2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7903146 2.00E-51 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001198526 TCF7L2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7903146 3.00E-23 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001198526 TCF7L2 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs7903146 5.00E-08 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_001198526 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 6.00E-16 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001198526 TCF7L2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs7903146 7.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001198526 TCF7L2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs7903146 8.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001198526 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 9.00E-30 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001198526 TCF7L2 20849430 http://www.ncbi.nlm.nih.gov/pubmed/20849430 "Hemoglobin A, Glycosylated" rs7903146 1.00E-07 The TCF7L2 diabetes risk variant is associated with HbAG??(C) levels: a genome-wide association meta-analysis. NHGRI|-1
NM_001198526 TCF7L2 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs12243326 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001198526 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12255372 1.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001198527 TCF7L2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7901695 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001198527 TCF7L2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs7901695 1.00E-48 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001198527 TCF7L2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs4506565 5.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001198527 TCF7L2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4506565 1.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001198527 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.25E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001198527 TCF7L2 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs7903146 1.00E-30 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001198527 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001198527 TCF7L2 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs7903146 2.00E-10 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001198527 TCF7L2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs7903146 2.00E-31 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001198527 TCF7L2 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs7903146 2.00E-34 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001198527 TCF7L2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7903146 2.00E-51 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001198527 TCF7L2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7903146 3.00E-23 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001198527 TCF7L2 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs7903146 5.00E-08 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_001198527 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 6.00E-16 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001198527 TCF7L2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs7903146 7.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001198527 TCF7L2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs7903146 8.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001198527 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 9.00E-30 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001198527 TCF7L2 20849430 http://www.ncbi.nlm.nih.gov/pubmed/20849430 "Hemoglobin A, Glycosylated" rs7903146 1.00E-07 The TCF7L2 diabetes risk variant is associated with HbAG??(C) levels: a genome-wide association meta-analysis. NHGRI|-1
NM_001198527 TCF7L2 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs12243326 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001198527 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12255372 1.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001198528 TCF7L2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7901695 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001198528 TCF7L2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs7901695 1.00E-48 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001198528 TCF7L2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs4506565 5.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001198528 TCF7L2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4506565 1.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001198528 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.25E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001198528 TCF7L2 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs7903146 1.00E-30 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001198528 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001198528 TCF7L2 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs7903146 2.00E-10 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001198528 TCF7L2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs7903146 2.00E-31 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001198528 TCF7L2 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs7903146 2.00E-34 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001198528 TCF7L2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7903146 2.00E-51 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001198528 TCF7L2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7903146 3.00E-23 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001198528 TCF7L2 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs7903146 5.00E-08 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_001198528 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 6.00E-16 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001198528 TCF7L2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs7903146 7.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001198528 TCF7L2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs7903146 8.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001198528 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 9.00E-30 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001198528 TCF7L2 20849430 http://www.ncbi.nlm.nih.gov/pubmed/20849430 "Hemoglobin A, Glycosylated" rs7903146 1.00E-07 The TCF7L2 diabetes risk variant is associated with HbAG??(C) levels: a genome-wide association meta-analysis. NHGRI|-1
NM_001198528 TCF7L2 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs12243326 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001198528 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12255372 1.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001198529 TCF7L2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7901695 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001198529 TCF7L2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs7901695 1.00E-48 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001198529 TCF7L2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs4506565 5.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001198529 TCF7L2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4506565 1.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001198529 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.25E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001198529 TCF7L2 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs7903146 1.00E-30 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001198529 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001198529 TCF7L2 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs7903146 2.00E-10 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001198529 TCF7L2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs7903146 2.00E-31 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001198529 TCF7L2 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs7903146 2.00E-34 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001198529 TCF7L2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7903146 2.00E-51 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001198529 TCF7L2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7903146 3.00E-23 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001198529 TCF7L2 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs7903146 5.00E-08 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_001198529 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 6.00E-16 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001198529 TCF7L2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs7903146 7.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001198529 TCF7L2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs7903146 8.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001198529 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 9.00E-30 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001198529 TCF7L2 20849430 http://www.ncbi.nlm.nih.gov/pubmed/20849430 "Hemoglobin A, Glycosylated" rs7903146 1.00E-07 The TCF7L2 diabetes risk variant is associated with HbAG??(C) levels: a genome-wide association meta-analysis. NHGRI|-1
NM_001198529 TCF7L2 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs12243326 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001198529 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12255372 1.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001198531 TCF7L2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7901695 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001198531 TCF7L2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs7901695 1.00E-48 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_001198531 TCF7L2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs4506565 5.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001198531 TCF7L2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4506565 1.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001198531 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.25E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001198531 TCF7L2 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs7903146 1.00E-30 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_001198531 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_001198531 TCF7L2 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs7903146 2.00E-10 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_001198531 TCF7L2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs7903146 2.00E-31 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001198531 TCF7L2 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs7903146 2.00E-34 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_001198531 TCF7L2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7903146 2.00E-51 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001198531 TCF7L2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7903146 3.00E-23 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001198531 TCF7L2 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs7903146 5.00E-08 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_001198531 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 6.00E-16 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001198531 TCF7L2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs7903146 7.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001198531 TCF7L2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs7903146 8.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_001198531 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 9.00E-30 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_001198531 TCF7L2 20849430 http://www.ncbi.nlm.nih.gov/pubmed/20849430 "Hemoglobin A, Glycosylated" rs7903146 1.00E-07 The TCF7L2 diabetes risk variant is associated with HbAG??(C) levels: a genome-wide association meta-analysis. NHGRI|-1
NM_001198531 TCF7L2 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs12243326 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001198531 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12255372 1.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001198541 ERAP1 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs27524 3.00E-11 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_001198541 ERAP1 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Aminopeptidases rs13160562 7.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_001198541 ERAP1 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs30187 2.00E-27 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_001198541 ERAP1 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs27434 5.00E-12 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_001198546 NOL4 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs7239368 9.00E-06 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_001198546 NOL4 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs1013696 4.00E-06 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_001198547 NOL4 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs7239368 9.00E-06 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_001198547 NOL4 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs1013696 4.00E-06 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_001198548 NOL4 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs7239368 9.00E-06 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_001198548 NOL4 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs1013696 4.00E-06 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_001198549 NOL4 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs7239368 9.00E-06 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_001198549 NOL4 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs1013696 4.00E-06 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_001198551 WT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs11031676 5.68E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001198551 WT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7944342 6.98E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001198552 WT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs11031676 5.68E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001198552 WT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7944342 6.98E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001198559 DNAJC27 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs4665736 7.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001198559 DNAJC27 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs713586 6.00E-22 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001198656 AKAP2 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs7032940 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_001198681 LEPROT 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs1892534 7.00E-21 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_001198681 LEPROT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs1892534 4.77E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001198681 LEPROT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs2889195 5.95E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001198681 LEPROT 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4420065 4.00E-62 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001198681 LEPROT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs4420065 6.67E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001198681 LEPROT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs12753193 3.76E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001198681 LEPROT 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Inflammation rs12753193 4.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001198683 LEPROT 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs1892534 7.00E-21 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_001198683 LEPROT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs1892534 4.77E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001198683 LEPROT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs2889195 5.95E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001198683 LEPROT 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4420065 4.00E-62 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001198683 LEPROT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs4420065 6.67E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001198683 LEPROT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs12753193 3.76E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_001198683 LEPROT 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Inflammation rs12753193 4.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001198687 LEPR 20167575 http://www.ncbi.nlm.nih.gov/pubmed/20167575 "Receptors, Leptin" rs1751492 6.00E-13 Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels. NHGRI|-1
NM_001198687 LEPR 19567438 http://www.ncbi.nlm.nih.gov/pubmed/19567438 C-Reactive Protein rs6700896 3.00E-14 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. NHGRI|-1
NM_001198688 LEPR 20167575 http://www.ncbi.nlm.nih.gov/pubmed/20167575 "Receptors, Leptin" rs1751492 6.00E-13 Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels. NHGRI|-1
NM_001198688 LEPR 19567438 http://www.ncbi.nlm.nih.gov/pubmed/19567438 C-Reactive Protein rs6700896 3.00E-14 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. NHGRI|-1
NM_001198689 LEPR 20167575 http://www.ncbi.nlm.nih.gov/pubmed/20167575 "Receptors, Leptin" rs1751492 6.00E-13 Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels. NHGRI|-1
NM_001198689 LEPR 19567438 http://www.ncbi.nlm.nih.gov/pubmed/19567438 C-Reactive Protein rs6700896 3.00E-14 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. NHGRI|-1
NM_001198777 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7920095 2.20E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198777 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7923172 1.43E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198777 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11595898 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198777 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934704 1.48E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198777 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1926554 3.32E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198777 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7099036 2.13E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198777 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934719 2.68E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198777 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198777 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198777 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198777 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2492448 3.84E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198777 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11591754 1.68E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198777 CUL2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs17582416 2.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001198778 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7920095 2.20E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198778 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7923172 1.43E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198778 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11595898 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198778 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934704 1.48E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198778 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1926554 3.32E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198778 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7099036 2.13E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198778 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934719 2.68E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198778 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198778 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198778 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198778 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2492448 3.84E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198778 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11591754 1.68E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198778 CUL2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs17582416 2.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001198779 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7920095 2.20E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198779 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7923172 1.43E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198779 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11595898 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198779 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934704 1.48E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198779 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1926554 3.32E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198779 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7099036 2.13E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198779 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934719 2.68E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198779 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198779 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198779 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198779 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2492448 3.84E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198779 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11591754 1.68E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198779 CUL2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs17582416 2.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001198783 POU2F1 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs9803659 4.00E-06 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_001198786 POU2F1 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs9803659 4.00E-06 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_001198853 CYP2C8 18594024 http://www.ncbi.nlm.nih.gov/pubmed/18594024 Osteonecrosis rs1934951 1.00E-06 Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis. NHGRI|-1
NM_001198853 CYP2C8 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs2185570 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001198854 CYP2C8 18594024 http://www.ncbi.nlm.nih.gov/pubmed/18594024 Osteonecrosis rs1934951 1.00E-06 Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis. NHGRI|-1
NM_001198854 CYP2C8 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs2185570 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001198855 CYP2C8 18594024 http://www.ncbi.nlm.nih.gov/pubmed/18594024 Osteonecrosis rs1934951 1.00E-06 Bisphosphonate-related osteonecrosis of the jaw is associated with polymorphisms of the cytochrome P450 CYP2C8 in multiple myeloma: a genome-wide single nucleotide polymorphism analysis. NHGRI|-1
NM_001198855 CYP2C8 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs2185570 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs7756516 5.36E-112 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001198858 HLA-DQB2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs7756516 3.02E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2301271 2.38E-100 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001198858 HLA-DQB2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2301271 2.89E-15 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001198858 HLA-DQB2 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs2301271 2.00E-12 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs7768538 4.59E-15 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs7453920 6.84E-100 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001198858 HLA-DQB2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs7453920 3.77E-15 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs7453920 3.99E-15 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2051549 1.67E-15 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2051549 7.98E-15 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2071550 1.29E-95 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1573649 1.03E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001198858 HLA-DQB2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1573649 2.00E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6902723 8.63E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs6903130 6.43E-72 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001198858 HLA-DQB2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs6903130 4.43E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6903130 1.70E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9296044 2.95E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs6901084 1.21E-85 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9368741 3.26E-95 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2857210 4.10E-14 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9276644 2.04E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7762279 2.40E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001198858 HLA-DQB2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs7762279 2.97E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001198858 HLA-DQB2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs7758736 1.15E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7758736 3.07E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2621384 4.64E-14 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2857161 8.19E-14 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2621383 9.05E-14 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2621382 3.11E-10 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2157082 1.34E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2857154 6.68E-12 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9276726 1.28E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs7767167 9.33E-68 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2219893 2.56E-68 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2857136 4.56E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2857129 3.53E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001198858 HLA-DQB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs10807113 7.00E-112 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001198858 HLA-DQB2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10807113 2.18E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001198899 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs651905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198899 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs602905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198900 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs651905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198900 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs602905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198901 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs651905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198901 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs602905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198902 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs651905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198902 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs602905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198903 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs651905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198903 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs602905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198904 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs651905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198904 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs602905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198905 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs651905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198905 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs602905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198906 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs651905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198906 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs602905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9521061 1.33E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1041466 3.67E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1041466 4.00E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1411766 1.82E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1411766 8.15E-06 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17412858 2.11E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17412858 9.68E-06 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6492208 2.03E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6492208 7.41E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2391777 1.12E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2391777 3.42E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2391778 2.08E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2391778 8.33E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9515085 1.40E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9515085 4.40E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1411765 2.01E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1411765 8.24E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7989848 4.14E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7989848 7.02E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1929210 3.77E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9521445 1.21E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001198950 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9521445 2.95E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001198950 MYO16 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4772972 7.05E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001198965 NFATC4 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs1950500 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001198966 NFATC4 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs1950500 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001198967 NFATC4 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs1950500 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001198999 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs12594515 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001198999 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs12594515 7.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001198999 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4603502 3.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198999 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1865648 1.57E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001198999 SEMA6D 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11857760 6.14E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001199086 NT5C1B 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognition rs1876040 6.00E-08 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001199087 NT5C1B 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognition rs1876040 6.00E-08 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001199088 NT5C1B 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognition rs1876040 6.00E-08 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001199096 BAIAP3 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4984814 2.79E-08 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001199097 BAIAP3 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4984814 2.79E-08 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001199098 BAIAP3 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4984814 2.79E-08 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001199099 BAIAP3 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4984814 2.79E-08 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001199135 TANK 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs10192369 9.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001199135 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6432628 9.13E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001199135 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13034284 1.85E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001199135 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9967749 8.13E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001199135 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11681327 4.77E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001199135 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7603576 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001199135 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2551691 9.03E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001199135 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs197275 4.42E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001199143 XIRP2 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs13015447 7.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001199144 XIRP2 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs13015447 7.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001199145 XIRP2 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs13015447 7.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001199148 SLC38A11 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Foot rs776488 2.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_001199148 SLC38A11 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs13424957 3.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001199149 LTF 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs1015164 9.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_001199159 PI16 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs1405069 6.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NM_001199165 CCDC46 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs8074751 1.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_001199165 CCDC46 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs7209395 3.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001199165 CCDC46 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs757558 6.42E-06 NBL-GWAS version 1 dbGaP|2845
NM_001199172 MGAT5B 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9916886 4.52E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001199173 MLST8 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs26868 9.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001199174 MLST8 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs26868 9.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001199175 MLST8 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs26868 9.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001199208 CYP4F2 19578179 http://www.ncbi.nlm.nih.gov/pubmed/19578179 Acenocoumarol rs2108622 3.00E-10 A genome-wide association study of acenocoumarol maintenance dosage. NHGRI|-1
NM_001199208 CYP4F2 21729881 http://www.ncbi.nlm.nih.gov/pubmed/21729881 Vitamin E rs2108622 1.00E-10 Genome-wide association study identifies common variants associated with circulating vitamin E levels NHGRI|-1
NM_001199208 CYP4F2 19300499 http://www.ncbi.nlm.nih.gov/pubmed/19300499 Warfarin rs2108622 3.00E-10 "A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose." NHGRI|-1
NM_001199208 CYP4F2 20833655 http://www.ncbi.nlm.nih.gov/pubmed/20833655 Warfarin rs2108622 3.00E-08 Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. NHGRI|-1
NM_001199209 CYP4F2 19578179 http://www.ncbi.nlm.nih.gov/pubmed/19578179 Acenocoumarol rs2108622 3.00E-10 A genome-wide association study of acenocoumarol maintenance dosage. NHGRI|-1
NM_001199209 CYP4F2 21729881 http://www.ncbi.nlm.nih.gov/pubmed/21729881 Vitamin E rs2108622 1.00E-10 Genome-wide association study identifies common variants associated with circulating vitamin E levels NHGRI|-1
NM_001199209 CYP4F2 19300499 http://www.ncbi.nlm.nih.gov/pubmed/19300499 Warfarin rs2108622 3.00E-10 "A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose." NHGRI|-1
NM_001199209 CYP4F2 20833655 http://www.ncbi.nlm.nih.gov/pubmed/20833655 Warfarin rs2108622 3.00E-08 Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. NHGRI|-1
NM_001199214 STMN2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11997947 9.55E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001199237 BAT4 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3130618 9.99E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001199238 BAT4 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3130618 9.99E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001199239 BAT4 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3130618 9.99E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001199240 BAT4 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3130618 9.99E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001199241 KYNU 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs352892 5.04E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001199241 KYNU 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2890652 1.00E-10 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001199251 SGOL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6776153 9.43E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001199251 SGOL1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs11720452 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001199251 SGOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1395993 3.49E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001199252 SGOL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6776153 9.43E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001199252 SGOL1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs11720452 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001199252 SGOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1395993 3.49E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001199253 SGOL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6776153 9.43E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001199253 SGOL1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs11720452 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001199253 SGOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1395993 3.49E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001199254 SGOL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6776153 9.43E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001199254 SGOL1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs11720452 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001199254 SGOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1395993 3.49E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001199255 SGOL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6776153 9.43E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001199255 SGOL1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs11720452 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001199255 SGOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1395993 3.49E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001199256 SGOL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6776153 9.43E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001199256 SGOL1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs11720452 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001199256 SGOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1395993 3.49E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001199257 SGOL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6776153 9.43E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001199257 SGOL1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs11720452 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001199257 SGOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1395993 3.49E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001199261 UCHL5 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs9427573 5.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_001199261 UCHL5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs842796 7.60E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001199261 UCHL5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs842796 8.50E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001199262 UCHL5 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs9427573 5.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_001199262 UCHL5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs842796 7.60E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001199262 UCHL5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs842796 8.50E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001199263 UCHL5 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs9427573 5.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_001199263 UCHL5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs842796 7.60E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001199263 UCHL5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs842796 8.50E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001199266 DGKZ 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11038871 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_001199267 DGKZ 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11038871 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_001199268 DGKZ 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11038871 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_001199280 HAS3 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs8047014 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001199297 UIMC1 19448621 http://www.ncbi.nlm.nih.gov/pubmed/19448621 Menarche rs365132 8.00E-14 Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. NHGRI|-1
NM_001199298 UIMC1 19448621 http://www.ncbi.nlm.nih.gov/pubmed/19448621 Menarche rs365132 8.00E-14 Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. NHGRI|-1
NM_001199302 CNOT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs10506584 3.03E-05 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_001199302 CNOT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1882191 7.52E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001199303 CNOT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs10506584 3.03E-05 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_001199303 CNOT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1882191 7.52E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001199319 PEX26 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs462904 3.01E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001199324 ZNF615 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11878803 1.07E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001199327 TNNI3K 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs1514175 8.00E-14 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001199346 C18orf32 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs8099594 3.00E-07 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001199377 ACSBG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11072744 7.62E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001199377 ACSBG1 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Exploratory Behavior rs1533665 7.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_001199380 RNF145 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs1473247 3.00E-07 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001199381 RNF145 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs1473247 3.00E-07 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001199382 RNF145 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs1473247 3.00E-07 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001199383 RNF145 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs1473247 3.00E-07 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001199427 TRAF3 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs10133111 5.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_001199479 ZNF193 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs9380069 1.38E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001199479 ZNF193 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs967005 3.38E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001199479 ZNF193 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs9380064 3.75E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001199480 ZNF193 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs9380069 1.38E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001199480 ZNF193 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs967005 3.38E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001199480 ZNF193 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs9380064 3.75E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001199509 NCR2 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs9471576 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001199510 NCR2 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs9471576 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001199562 PLA2G6 19578365 http://www.ncbi.nlm.nih.gov/pubmed/19578365 Dysplastic Nevus Syndrome rs2284063 3.00E-08 Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. NHGRI|-1
NM_001199562 PLA2G6 19578364 http://www.ncbi.nlm.nih.gov/pubmed/19578364 Melanoma rs2284063 2.00E-09 Genome-wide association study identifies three loci associated with melanoma risk. NHGRI|-1
NM_001199562 PLA2G6 21478494 http://www.ncbi.nlm.nih.gov/pubmed/21478494 Cutaneous nevi rs738322 1.00E-06 Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk. NHGRI|-1
NM_001199633 SLC28A3 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, HDL" rs10123041 6.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001199635 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2267727 3.79E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001199635 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2267742 4.79E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001199635 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1558477 2.58E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001199635 ADCYAP1R1 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1558477 3.00E-07 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001199635 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7791986 8.41E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001199636 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2267727 3.79E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001199636 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2267742 4.79E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001199636 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1558477 2.58E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001199636 ADCYAP1R1 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1558477 3.00E-07 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001199636 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7791986 8.41E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001199637 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2267727 3.79E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001199637 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2267742 4.79E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001199637 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1558477 2.58E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001199637 ADCYAP1R1 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1558477 3.00E-07 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_001199637 ADCYAP1R1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7791986 8.41E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001199640 IL33 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs1342326 9.00E-10 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_001199641 IL33 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs1342326 9.00E-10 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_001199642 ADCY5 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs11708067 7.00E-22 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001199642 ADCY5 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs11708067 3.00E-12 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001199642 ADCY5 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs2877716 7.00E-16 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001199642 ADCY5 20372150 http://www.ncbi.nlm.nih.gov/pubmed/20372150 Birth Weight rs9883204 7.00E-15 Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. NHGRI|-1
NM_001199653 PMF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1052067 5.12E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001199654 PMF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1052067 5.12E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001199661 PMF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1052067 5.12E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001199662 PMF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1052067 5.12E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001199663 PMF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1052067 5.12E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001199679 TMEM56 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1414896 2.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001199687 EDA2R 18849991 http://www.ncbi.nlm.nih.gov/pubmed/18849991 Alopecia rs6625163 5.00E-11 Male-pattern baldness susceptibility locus at 20p11. NHGRI|-1
NM_001199697 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1077393 3.83E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001199697 BAT3 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs760293 9.72E-20 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001199697 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs805303 2.79E-119 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001199697 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs805303 1.25E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001199697 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3130050 1.52E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001199697 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3117583 3.33E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001199697 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3117582 2.62E-83 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001199697 BAT3 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs3117582 4.00E-10 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_001199697 BAT3 18978787 http://www.ncbi.nlm.nih.gov/pubmed/18978787 Lung Neoplasms rs3117582 5.00E-10 Common 5p15.33 and 6p21.33 variants influence lung cancer risk. NHGRI|-1
NM_001199697 BAT3 19836008 http://www.ncbi.nlm.nih.gov/pubmed/19836008 Lung Neoplasms rs3117582 5.00E-12 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. NHGRI|-1
NM_001199697 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3117582 4.53E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001199698 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1077393 3.83E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001199698 BAT3 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs760293 9.72E-20 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001199698 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs805303 2.79E-119 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001199698 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs805303 1.25E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001199698 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3130050 1.52E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001199698 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3117583 3.33E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001199698 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3117582 2.62E-83 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001199698 BAT3 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs3117582 4.00E-10 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_001199698 BAT3 18978787 http://www.ncbi.nlm.nih.gov/pubmed/18978787 Lung Neoplasms rs3117582 5.00E-10 Common 5p15.33 and 6p21.33 variants influence lung cancer risk. NHGRI|-1
NM_001199698 BAT3 19836008 http://www.ncbi.nlm.nih.gov/pubmed/19836008 Lung Neoplasms rs3117582 5.00E-12 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. NHGRI|-1
NM_001199698 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3117582 4.53E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001199729 MSRA 21679298 http://www.ncbi.nlm.nih.gov/pubmed/21679298 Schizophrenia rs7017212 4.00E-06 A genome-wide association study for quantitative traits in schizophrenia in China. NHGRI|-1
NM_001199729 MSRA 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs11775334 4.00E-06 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001199729 MSRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6992153 9.14E-05 NBL-GWAS version 2 dbGaP|2895
NM_001199729 MSRA 20452100 http://www.ncbi.nlm.nih.gov/pubmed/20452100 Neurofibrillary Tangles rs11782819 3.00E-06 Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study. NHGRI|-1
NM_001199729 MSRA 19557161 http://www.ncbi.nlm.nih.gov/pubmed/19557161 Adiposity rs545854 9.00E-09 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. NHGRI|-1
NM_001199729 MSRA 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs545854 3.57E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001199746 HOXD8 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs2592394 5.00E-07 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001199747 HOXD8 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs2592394 5.00E-07 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001199756 PPP2R5A 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs351408 5.86E-06 NBL-GWAS version 1 dbGaP|2845
NM_001199770 OTX1 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs6545977 5.00E-07 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001199772 PSMA5 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs1933182 1.00E-07 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001199773 PSMA5 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs1933182 1.00E-07 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001199774 PSMA5 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs1933182 1.00E-07 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001199777 POC1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs770374 5.30E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001199779 PSMB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6688464 6.00E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001199780 PSMB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6688464 6.00E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001199781 POC1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs770374 5.30E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001199782 POC1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs770374 5.30E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001199799 ILDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11718322 8.23E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001199800 ILDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11718322 8.23E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001199803 CENPO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs41523444 1.63E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001199803 CENPO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs35213472 6.98E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001199814 ZNF812 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2112837 5.59E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001199835 SNX10 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4563785 4.83E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001199835 SNX10 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4563785 6.51E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001199835 SNX10 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4563785 3.60E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001199835 SNX10 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs886716 8.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001199837 SNX10 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4563785 4.83E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001199837 SNX10 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4563785 6.51E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001199837 SNX10 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4563785 3.60E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001199837 SNX10 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs886716 8.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001199838 SNX10 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4563785 4.83E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001199838 SNX10 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4563785 6.51E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001199838 SNX10 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4563785 3.60E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001199838 SNX10 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs886716 8.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001199847 SMURF1 20228798 http://www.ncbi.nlm.nih.gov/pubmed/20228798 "Colitis, Ulcerative" rs7809799 9.00E-11 Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). NHGRI|-1
NM_001199852 AK3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs385893 9.00E-17 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001199853 AK3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs385893 9.00E-17 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001199854 AK3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs385893 9.00E-17 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001199855 AK3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs385893 9.00E-17 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001199856 AK3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs385893 9.00E-17 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001199859 ANGPT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7818981 9.90E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001199859 ANGPT1 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs4534106 1.00E-06 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001199859 ANGPT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4734938 8.67E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001199866 KIF16B 21139019 http://www.ncbi.nlm.nih.gov/pubmed/21139019 Carcinoid Tumor rs2208059 4.00E-07 A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum. NHGRI|-1
NM_001199868 GLRX3 19786962 http://www.ncbi.nlm.nih.gov/pubmed/19786962 Speech Perception rs4751178 7.00E-06 First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. NHGRI|-1
NM_001199868 GLRX3 21160409 http://www.ncbi.nlm.nih.gov/pubmed/21160409 HIV-1 rs4751185 7.00E-06 Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population. NHGRI|-1
NM_001199886 IL7 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs2717536 1.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001199886 IL7 19081515 http://www.ncbi.nlm.nih.gov/pubmed/19081515 Creutzfeldt-Jakob Syndrome rs1460163 6.00E-08 Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. NHGRI|-1
NM_001199887 IL7 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs2717536 1.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001199887 IL7 19081515 http://www.ncbi.nlm.nih.gov/pubmed/19081515 Creutzfeldt-Jakob Syndrome rs1460163 6.00E-08 Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. NHGRI|-1
NM_001199888 IL7 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs2717536 1.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001199888 IL7 19081515 http://www.ncbi.nlm.nih.gov/pubmed/19081515 Creutzfeldt-Jakob Syndrome rs1460163 6.00E-08 Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. NHGRI|-1
NM_001199922 SIAE 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs544368 6.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001200 BMP2 18759275 http://www.ncbi.nlm.nih.gov/pubmed/18759275 Uric Acid rs6085920 6.00E-06 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. NHGRI|-1
NM_001200 BMP2 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Count rs6108011 6.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001200 BMP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs6108011 5.12E-04 Genome-wide association between genotype and incident stroke in participants of primarily self-described European ancestry dbGaP|2886
NM_001200 BMP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6038449 5.19E-05 NBL-GWAS version 2 dbGaP|2895
NM_001200 BMP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2209761 5.14E-05 NBL-GWAS version 2 dbGaP|2895
NM_001200 BMP2 19011631 http://www.ncbi.nlm.nih.gov/pubmed/19011631 Colorectal Neoplasms rs961253 2.00E-10 Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. NHGRI|-1
NM_001200 BMP2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs967417 2.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001200 BMP2 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs2145270 6.00E-06 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_001200001 NOTCH2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs10923931 4.00E-08 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001201325 PDZK1 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs1967017 4.00E-08 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_001201325 PDZK1 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs12129861 3.00E-09 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_001201326 PDZK1 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs1967017 4.00E-08 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_001201326 PDZK1 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs12129861 3.00E-09 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_001201329 PPP1R3B 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs9987289 3.00E-13 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001201329 PPP1R3B 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs9987289 1.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001201329 PPP1R3B 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs9987289 4.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001201329 PPP1R3B 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs6601299 1.00E-08 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001201329 PPP1R3B 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs2126259 7.00E-12 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001201329 PPP1R3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9329191 6.16E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001201329 PPP1R3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12334460 2.92E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001201365 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs252139 7.04E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001201365 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs252095 4.58E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001201365 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs409037 4.58E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001201377 ALDH7A1 20072603 http://www.ncbi.nlm.nih.gov/pubmed/20072603 Osteoporosis rs13182402 2.00E-09 Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis. NHGRI|-1
NM_001201397 EDNRB 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs9574199 7.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_001201397 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6563036 6.86E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001201397 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7996252 2.72E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001201397 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7996252 8.44E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001201397 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2248525 3.14E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001201397 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2248525 8.12E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001201397 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2265775 5.77E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001201397 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2987526 3.23E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001201401 GALC 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs11624056 3.00E-08 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001201401 GALC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1385397 5.84E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001201401 GALC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2401711 9.82E-05 NBL-GWAS version 2 dbGaP|2895
NM_001201401 GALC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7152233 7.28E-06 NBL-GWAS version 2 dbGaP|2895
NM_001201402 GALC 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs11624056 3.00E-08 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001201402 GALC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1385397 5.84E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001201402 GALC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2401711 9.82E-05 NBL-GWAS version 2 dbGaP|2895
NM_001201402 GALC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7152233 7.28E-06 NBL-GWAS version 2 dbGaP|2895
NM_001201427 DAAM2 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs2395730 8.00E-08 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_001201428 GORASP2 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs4668356 5.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001201428 GORASP2 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs4668356 1.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001201428 GORASP2 18759275 http://www.ncbi.nlm.nih.gov/pubmed/18759275 Uric Acid rs4668338 3.00E-06 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. NHGRI|-1
NM_001201450 FLJ42280 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs4729260 2.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001201450 FLJ42280 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7781370 5.00E-12 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001201450 SHFM1 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs12669076 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_001201450 SHFM1 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs17598306 9.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_001201451 FLJ42280 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs4729260 2.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001201451 FLJ42280 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7781370 5.00E-12 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_001201466 ROPN1L 21424380 http://www.ncbi.nlm.nih.gov/pubmed/21424380 Breast Neoplasms rs1092913 2.00E-06 Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility. NHGRI|-1
NM_001201528 PCSK2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs4814615 5.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001201528 PCSK2 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Fibrinogen rs6044777 8.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001201528 PCSK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs6044777 2.96E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_001201528 PCSK2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs852069 3.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001201529 PCSK2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs4814615 5.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001201529 PCSK2 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Fibrinogen rs6044777 8.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001201529 PCSK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs6044777 2.96E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_001201529 PCSK2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs852069 3.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6685931 1.42E-61 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6685931 2.61E-73 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1853883 1.08E-22 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1853883 4.85E-15 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7522952 2.34E-17 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7522952 5.97E-16 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1853882 4.26E-11 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1971579 3.43E-10 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7548070 2.60E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7548070 4.93E-21 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4915318 5.49E-30 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4915318 5.91E-34 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7538501 2.02E-20 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7538501 7.55E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922144 1.53E-32 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922144 3.90E-37 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6657442 1.30E-38 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6657442 2.07E-33 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7517126 5.99E-20 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs13375144 5.05E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201550 CFHR4 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs6428370 7.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801575 1.13E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801575 7.31E-11 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001201550 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801575 8.31E-14 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6685931 1.42E-61 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6685931 2.61E-73 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1853883 1.08E-22 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1853883 4.85E-15 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7522952 2.34E-17 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7522952 5.97E-16 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1853882 4.26E-11 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1971579 3.43E-10 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7548070 2.60E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7548070 4.93E-21 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4915318 5.49E-30 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4915318 5.91E-34 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7538501 2.02E-20 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7538501 7.55E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922144 1.53E-32 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922144 3.90E-37 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6657442 1.30E-38 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6657442 2.07E-33 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7517126 5.99E-20 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs13375144 5.05E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201551 CFHR4 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs6428370 7.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801575 1.13E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801575 7.31E-11 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001201551 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801575 8.31E-14 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001201573 NUBPL 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs7142881 2.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001201573 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs8016004 3.64E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001201573 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2151784 3.65E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001201573 NUBPL 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2039485 6.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001201573 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6571481 1.55E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001201573 NUBPL 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs915071 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001201573 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs915071 4.18E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001201573 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs972396 7.82E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001201573 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1952966 4.84E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001201574 NUBPL 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs7142881 2.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_001201574 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs8016004 3.64E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001201574 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2151784 3.65E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001201574 NUBPL 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2039485 6.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001201574 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6571481 1.55E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001201574 NUBPL 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs915071 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001201574 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs915071 4.18E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001201574 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs972396 7.82E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001201574 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1952966 4.84E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001201576 PLSCR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4613118 8.86E-05 NBL-GWAS version 2 dbGaP|2895
NM_001201965 ASB3 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Hemoglobins rs1160297 1.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001201965 ASB3 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Hemoglobins rs2357013 6.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001202 BMP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12431733 1.52E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001202 BMP4 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs12431733 3.00E-06 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_001202 BMP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8005200 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001202 BMP4 19011631 http://www.ncbi.nlm.nih.gov/pubmed/19011631 Colorectal Neoplasms rs4444235 8.00E-10 Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. NHGRI|-1
NM_001202404 ALDH7A1 20072603 http://www.ncbi.nlm.nih.gov/pubmed/20072603 Osteoporosis rs13182402 2.00E-09 Genome-wide association study identifies ALDH7A1 as a novel susceptibility gene for osteoporosis. NHGRI|-1
NM_001202504 CTDP1 20801717 http://www.ncbi.nlm.nih.gov/pubmed/20801717 Amyotrophic Lateral Sclerosis rs4799088 9.00E-06 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. NHGRI|-1
NM_001202504 CTDP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs537962 1.39E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001202504 CTDP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4799092 2.00E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001202515 CFLAR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12621441 3.43E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001202516 CFLAR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12621441 3.43E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001202517 CFLAR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12621441 3.43E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001202518 CFLAR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12621441 3.43E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001202519 CFLAR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12621441 3.43E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264327 1.68E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2239518 3.45E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9468843 9.01E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3129975 2.40E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs12526186 1.27E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202521 DDR1 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs12526186 3.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001202521 DDR1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs6911628 2.20E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs4711229 5.43E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs3131043 1.76E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3131043 1.81E-11 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs34682678 1.68E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9295917 5.09E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs13198118 2.07E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264362 1.31E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202521 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs886424 4.70E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9295924 2.69E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs4713380 6.51E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs915664 8.45E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202521 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1264350 1.86E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7749924 2.25E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2535331 3.74E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2250264 8.16E-09 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202521 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2844659 1.23E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2535327 1.30E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844654 4.43E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264333 4.42E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264332 4.98E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264331 4.47E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202521 DDR1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs7756521 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001202521 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7756521 7.58E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264327 1.68E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2239518 3.45E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9468843 9.01E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3129975 2.40E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs12526186 1.27E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202523 DDR1 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs12526186 3.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001202523 DDR1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs6911628 2.20E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs4711229 5.43E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs3131043 1.76E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3131043 1.81E-11 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs34682678 1.68E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9295917 5.09E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs13198118 2.07E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264362 1.31E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202523 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs886424 4.70E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9295924 2.69E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs4713380 6.51E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs915664 8.45E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202523 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1264350 1.86E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7749924 2.25E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2535331 3.74E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2250264 8.16E-09 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202523 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2844659 1.23E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2535327 1.30E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844654 4.43E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264333 4.42E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264332 4.98E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264331 4.47E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001202523 DDR1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs7756521 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001202523 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7756521 7.58E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001202543 CUX1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2906724 3.94E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001202543 CUX1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11974778 8.09E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001202544 CUX1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2906724 3.94E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001202544 CUX1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11974778 8.09E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001202545 CUX1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2906724 3.94E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001202545 CUX1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11974778 8.09E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001202546 CUX1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2906724 3.94E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001202546 CUX1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11974778 8.09E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001202550 WDR27 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs3734905 2.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001202555 CD44 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2295756 9.65E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001202556 CD44 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2295756 9.65E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001202557 CD44 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2295756 9.65E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001203 BMPR1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6831418 1.50E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001203 BMPR1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs4538488 1.39E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001203 BMPR1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs4254781 1.91E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001203 BMPR1B 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs1859156 2.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_001203 BMPR1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11097457 1.97E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001203251 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17563986 3.44E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001203251 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs242557 9.00E-18 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_001203251 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1981997 2.02E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001203251 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs8070723 3.36E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001203251 MAPT 21044948 http://www.ncbi.nlm.nih.gov/pubmed/21044948 Parkinson Disease rs8070723 7.00E-12 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. NHGRI|-1
NM_001203251 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs8070723 2.00E-118 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_001203252 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17563986 3.44E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001203252 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs242557 9.00E-18 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_001203252 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1981997 2.02E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001203252 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs8070723 3.36E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001203252 MAPT 21044948 http://www.ncbi.nlm.nih.gov/pubmed/21044948 Parkinson Disease rs8070723 7.00E-12 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. NHGRI|-1
NM_001203252 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs8070723 2.00E-118 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_001203258 MTA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9743822 1.35E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001204056 ANKRD12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1114591 3.23E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001204065 ANKS1B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7968606 3.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001204065 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs2373011 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204065 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs2373011 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204065 ANKS1B 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11110077 4.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001204066 ANKS1B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7968606 3.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001204066 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs2373011 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204066 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs2373011 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204066 ANKS1B 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11110077 4.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001204067 ANKS1B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7968606 3.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001204067 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs2373011 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204067 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs2373011 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204067 ANKS1B 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11110077 4.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001204068 ANKS1B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7968606 3.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001204068 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs2373011 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204068 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs2373011 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204068 ANKS1B 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11110077 4.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001204069 ANKS1B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7968606 3.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001204069 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs2373011 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204069 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs2373011 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204069 ANKS1B 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11110077 4.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001204070 ANKS1B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7968606 3.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001204070 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs2373011 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204070 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs2373011 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204070 ANKS1B 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11110077 4.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001204078 ATP6V1G2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2251824 5.97E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001204078 ATP6V1G2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071593 4.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001204078 ATP6V1G2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2523503 5.59E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001204079 ANKS1B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7968606 3.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001204079 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs2373011 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204079 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs2373011 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204079 ANKS1B 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11110077 4.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001204080 ANKS1B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7968606 3.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001204080 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs2373011 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204080 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs2373011 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204080 ANKS1B 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11110077 4.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001204081 ANKS1B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7968606 3.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001204081 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs2373011 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204081 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs2373011 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204081 ANKS1B 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11110077 4.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001204082 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 2.00E-11 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001204082 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 3.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001204082 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12138950 3.00E-18 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001204082 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs10917468 1.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001204083 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 2.00E-11 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001204083 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 3.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001204083 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12138950 3.00E-18 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001204083 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs10917468 1.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001204087 KCNN3 20173747 http://www.ncbi.nlm.nih.gov/pubmed/20173747 Atrial Fibrillation rs13376333 2.00E-21 Common variants in KCNN3 are associated with lone atrial fibrillation. NHGRI|-1
NM_001204103 PPT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3134603 3.36E-116 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001204103 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3096697 2.16E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001204103 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3096697 5.66E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001204103 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130347 1.22E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001204103 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130347 3.62E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001204106 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001204106 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_001204107 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001204107 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_001204108 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001204108 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_001204109 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001204109 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_001204110 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001204110 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_001204111 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001204111 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_001204112 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001204112 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_001204113 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_001204113 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_001204144 HDAC9 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs615545 5.89E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001204145 HDAC9 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs615545 5.89E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001204146 HDAC9 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs615545 5.89E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001204147 HDAC9 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs615545 5.89E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001204148 HDAC9 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs615545 5.89E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001204171 MDM4 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs12143943 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001204172 MDM4 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs12143943 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001204197 NBEA 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs1777672 4.00E-07 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001204213 NOS1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs478597 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001204214 NOS1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs478597 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001204218 NOS1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs478597 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001204255 SCARB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6532244 2.09E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001204269 KCNA2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7526730 2.14E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001204269 KCNA2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6700661 4.20E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001204269 KCNA2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs17025978 6.56E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_001204269 KCNA2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7553815 3.96E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001204285 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001204285 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001204286 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001204286 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001204287 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001204287 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001204288 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001204288 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001204289 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001204289 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001204290 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001204290 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001204291 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001204291 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001204292 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001204292 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001204293 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001204293 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001204294 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001204294 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001204295 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001204295 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001204296 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001204296 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001204297 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001204297 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_001204298 ZNF664 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs4765078 1.67E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001204299 FAM101A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs4765078 1.67E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001204306 GC 20541252 http://www.ncbi.nlm.nih.gov/pubmed/20541252 Vitamin D rs2282679 2.00E-109 Common genetic determinants of vitamin D insufficiency: a genome-wide association study. NHGRI|-1
NM_001204306 GC 20418485 http://www.ncbi.nlm.nih.gov/pubmed/20418485 Vitamin D rs2282679 2.00E-49 Genome-wide association study of circulating vitamin D levels. NHGRI|-1
NM_001204307 GC 20541252 http://www.ncbi.nlm.nih.gov/pubmed/20541252 Vitamin D rs2282679 2.00E-109 Common genetic determinants of vitamin D insufficiency: a genome-wide association study. NHGRI|-1
NM_001204307 GC 20418485 http://www.ncbi.nlm.nih.gov/pubmed/20418485 Vitamin D rs2282679 2.00E-49 Genome-wide association study of circulating vitamin D levels. NHGRI|-1
NM_001204314 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286411 2.12E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204314 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 5.38E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001204314 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 6.67E-07 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204314 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs169587 1.61E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204314 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1605683 1.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204314 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286388 1.39E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204314 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 1.29E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204314 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 3.17E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001204315 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286411 2.12E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204315 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 5.38E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001204315 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 6.67E-07 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204315 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs169587 1.61E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204315 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1605683 1.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204315 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286388 1.39E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204315 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 1.29E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204315 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 3.17E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001204316 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286411 2.12E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204316 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 5.38E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001204316 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 6.67E-07 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204316 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs169587 1.61E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204316 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1605683 1.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204316 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286388 1.39E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204316 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 1.29E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204316 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 3.17E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001204317 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286411 2.12E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204317 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 5.38E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001204317 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 6.67E-07 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204317 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs169587 1.61E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204317 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1605683 1.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204317 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286388 1.39E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204317 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 1.29E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204317 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 3.17E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001204318 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286411 2.12E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204318 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 5.38E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001204318 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 6.67E-07 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204318 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs169587 1.61E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204318 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1605683 1.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204318 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286388 1.39E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204318 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 1.29E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001204318 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 3.17E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001204352 SPOCK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7657608 2.65E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001204353 SPOCK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7657608 2.65E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001204354 SPOCK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7657608 2.65E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001204355 SPOCK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7657608 2.65E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001204356 SPOCK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7657608 2.65E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001204357 SPOCK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7657608 2.65E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001204358 SPOCK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7657608 2.65E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001204359 SPOCK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7657608 2.65E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001204366 MGST2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs8192013 4.55E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001204367 MGST2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs8192013 4.55E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001204368 MGST2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs8192013 4.55E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001204384 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001204384 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001204384 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001204384 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001204384 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001204385 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_001204385 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001204385 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001204385 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_001204385 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001204397 PITX2 19597492 http://www.ncbi.nlm.nih.gov/pubmed/19597492 Atrial Fibrillation rs17042171 4.00E-63 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. NHGRI|-1
NM_001204397 PITX2 19597491 http://www.ncbi.nlm.nih.gov/pubmed/19597491 Atrial Fibrillation rs2200733 1.00E-14 A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. NHGRI|-1
NM_001204397 PITX2 17603472 http://www.ncbi.nlm.nih.gov/pubmed/17603472 Atrial Fibrillation rs2200733 3.00E-41 Variants conferring risk of atrial fibrillation on chromosome 4q25. NHGRI|-1
NM_001204397 PITX2 18991354 http://www.ncbi.nlm.nih.gov/pubmed/18991354 Stroke rs2200733 2.00E-10 Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. NHGRI|-1
NM_001204397 PITX2 20173747 http://www.ncbi.nlm.nih.gov/pubmed/20173747 Atrial Fibrillation rs6843082 3.00E-28 Common variants in KCNN3 are associated with lone atrial fibrillation. NHGRI|-1
NM_001204397 PITX2 17603472 http://www.ncbi.nlm.nih.gov/pubmed/17603472 Atrial Fibrillation rs10033464 7.00E-11 Variants conferring risk of atrial fibrillation on chromosome 4q25. NHGRI|-1
NM_001204397 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs10033464 5.70E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_001204397 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2654735 9.03E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001204397 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1806506 3.67E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001204398 PITX2 19597492 http://www.ncbi.nlm.nih.gov/pubmed/19597492 Atrial Fibrillation rs17042171 4.00E-63 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. NHGRI|-1
NM_001204398 PITX2 19597491 http://www.ncbi.nlm.nih.gov/pubmed/19597491 Atrial Fibrillation rs2200733 1.00E-14 A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. NHGRI|-1
NM_001204398 PITX2 17603472 http://www.ncbi.nlm.nih.gov/pubmed/17603472 Atrial Fibrillation rs2200733 3.00E-41 Variants conferring risk of atrial fibrillation on chromosome 4q25. NHGRI|-1
NM_001204398 PITX2 18991354 http://www.ncbi.nlm.nih.gov/pubmed/18991354 Stroke rs2200733 2.00E-10 Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. NHGRI|-1
NM_001204398 PITX2 20173747 http://www.ncbi.nlm.nih.gov/pubmed/20173747 Atrial Fibrillation rs6843082 3.00E-28 Common variants in KCNN3 are associated with lone atrial fibrillation. NHGRI|-1
NM_001204398 PITX2 17603472 http://www.ncbi.nlm.nih.gov/pubmed/17603472 Atrial Fibrillation rs10033464 7.00E-11 Variants conferring risk of atrial fibrillation on chromosome 4q25. NHGRI|-1
NM_001204398 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs10033464 5.70E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_001204398 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2654735 9.03E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001204398 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1806506 3.67E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001204399 PITX2 19597492 http://www.ncbi.nlm.nih.gov/pubmed/19597492 Atrial Fibrillation rs17042171 4.00E-63 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. NHGRI|-1
NM_001204399 PITX2 19597491 http://www.ncbi.nlm.nih.gov/pubmed/19597491 Atrial Fibrillation rs2200733 1.00E-14 A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. NHGRI|-1
NM_001204399 PITX2 17603472 http://www.ncbi.nlm.nih.gov/pubmed/17603472 Atrial Fibrillation rs2200733 3.00E-41 Variants conferring risk of atrial fibrillation on chromosome 4q25. NHGRI|-1
NM_001204399 PITX2 18991354 http://www.ncbi.nlm.nih.gov/pubmed/18991354 Stroke rs2200733 2.00E-10 Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. NHGRI|-1
NM_001204399 PITX2 20173747 http://www.ncbi.nlm.nih.gov/pubmed/20173747 Atrial Fibrillation rs6843082 3.00E-28 Common variants in KCNN3 are associated with lone atrial fibrillation. NHGRI|-1
NM_001204399 PITX2 17603472 http://www.ncbi.nlm.nih.gov/pubmed/17603472 Atrial Fibrillation rs10033464 7.00E-11 Variants conferring risk of atrial fibrillation on chromosome 4q25. NHGRI|-1
NM_001204399 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs10033464 5.70E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_001204399 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2654735 9.03E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001204399 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1806506 3.67E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001204403 ANK3 20185149 http://www.ncbi.nlm.nih.gov/pubmed/20185149 Schizophrenia rs10761482 8.00E-06 Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. NHGRI|-1
NM_001204403 ANK3 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs10994336 9.00E-09 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001204403 ANK3 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs10994338 5.00E-07 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001204404 ANK3 20185149 http://www.ncbi.nlm.nih.gov/pubmed/20185149 Schizophrenia rs10761482 8.00E-06 Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. NHGRI|-1
NM_001204404 ANK3 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs10994336 9.00E-09 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_001204404 ANK3 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs10994338 5.00E-07 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_001204408 SEC14L1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs3744064 7.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001204410 SEC14L1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs3744064 7.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001204416 RGS6 20811658 http://www.ncbi.nlm.nih.gov/pubmed/20811658 Smoking Cessation rs7159300 4.00E-06 Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement. NHGRI|-1
NM_001204416 RGS6 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4903031 5.00E-06 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001204417 RGS6 20811658 http://www.ncbi.nlm.nih.gov/pubmed/20811658 Smoking Cessation rs7159300 4.00E-06 Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement. NHGRI|-1
NM_001204417 RGS6 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4903031 5.00E-06 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001204418 RGS6 20811658 http://www.ncbi.nlm.nih.gov/pubmed/20811658 Smoking Cessation rs7159300 4.00E-06 Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement. NHGRI|-1
NM_001204418 RGS6 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4903031 5.00E-06 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001204419 RGS6 20811658 http://www.ncbi.nlm.nih.gov/pubmed/20811658 Smoking Cessation rs7159300 4.00E-06 Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement. NHGRI|-1
NM_001204419 RGS6 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4903031 5.00E-06 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001204420 RGS6 20811658 http://www.ncbi.nlm.nih.gov/pubmed/20811658 Smoking Cessation rs7159300 4.00E-06 Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement. NHGRI|-1
NM_001204420 RGS6 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4903031 5.00E-06 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001204421 RGS6 20811658 http://www.ncbi.nlm.nih.gov/pubmed/20811658 Smoking Cessation rs7159300 4.00E-06 Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement. NHGRI|-1
NM_001204421 RGS6 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4903031 5.00E-06 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001204422 RGS6 20811658 http://www.ncbi.nlm.nih.gov/pubmed/20811658 Smoking Cessation rs7159300 4.00E-06 Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement. NHGRI|-1
NM_001204422 RGS6 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4903031 5.00E-06 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001204423 RGS6 20811658 http://www.ncbi.nlm.nih.gov/pubmed/20811658 Smoking Cessation rs7159300 4.00E-06 Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement. NHGRI|-1
NM_001204423 RGS6 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4903031 5.00E-06 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001204424 RGS6 20811658 http://www.ncbi.nlm.nih.gov/pubmed/20811658 Smoking Cessation rs7159300 4.00E-06 Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement. NHGRI|-1
NM_001204424 RGS6 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4903031 5.00E-06 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001204458 TNFRSF19 20512145 http://www.ncbi.nlm.nih.gov/pubmed/20512145 Nasopharyngeal Neoplasms rs9510787 2.00E-09 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. NHGRI|-1
NM_001204458 TNFRSF19 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs753955 2.00E-12 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_001204458 TNFRSF19 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9507108 2.60E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001204458 TNFRSF19 20512145 http://www.ncbi.nlm.nih.gov/pubmed/20512145 Nasopharyngeal Neoplasms rs1572072 1.00E-08 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. NHGRI|-1
NM_001204459 TNFRSF19 20512145 http://www.ncbi.nlm.nih.gov/pubmed/20512145 Nasopharyngeal Neoplasms rs9510787 2.00E-09 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. NHGRI|-1
NM_001204459 TNFRSF19 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs753955 2.00E-12 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_001204459 TNFRSF19 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9507108 2.60E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001204459 TNFRSF19 20512145 http://www.ncbi.nlm.nih.gov/pubmed/20512145 Nasopharyngeal Neoplasms rs1572072 1.00E-08 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. NHGRI|-1
NM_001204477 CDRT4 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Forced Expiratory Volume rs2906966 8.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_001204504 DGKH 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs6561030 7.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001204504 DGKH 17486107 http://www.ncbi.nlm.nih.gov/pubmed/17486107 Bipolar Disorder rs1012053 2.00E-08 A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder. NHGRI|-1
NM_001204504 DGKH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1886811 2.38E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001204505 DGKH 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs6561030 7.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001204505 DGKH 17486107 http://www.ncbi.nlm.nih.gov/pubmed/17486107 Bipolar Disorder rs1012053 2.00E-08 A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder. NHGRI|-1
NM_001204505 DGKH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1886811 2.38E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001204506 DGKH 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs6561030 7.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001204506 DGKH 17486107 http://www.ncbi.nlm.nih.gov/pubmed/17486107 Bipolar Disorder rs1012053 2.00E-08 A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder. NHGRI|-1
NM_001204506 DGKH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1886811 2.38E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001204514 KIFAP3 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs1541160 2.00E-08 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001204516 KIFAP3 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs1541160 2.00E-08 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001204517 KIFAP3 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs1541160 2.00E-08 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001204760 TLL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17689952 1.81E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001204798 KCNH2 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3807375 5.00E-11 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001204798 KCNH2 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs2968864 8.00E-16 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001204798 KCNH2 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs2968863 2.00E-15 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001204798 KCNH2 20062061 http://www.ncbi.nlm.nih.gov/pubmed/20062061 Electrocardiography rs4725982 3.00E-06 Genetic variation in SCN10A influences cardiac conduction. NHGRI|-1
NM_001204798 KCNH2 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs4725982 5.00E-16 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001204803 ANO6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12579771 2.29E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_001204813 NT5E 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11752804 1.30E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001204889 ALDH2 21372407 http://www.ncbi.nlm.nih.gov/pubmed/21372407 Drinking Behavior rs671 4.00E-211 Confirmation of ALDH2 as a Major locus of drinking behavior and of its variants regulating multiple metabolic phenotypes in a Japanese population. NHGRI|-1
NM_001204889 ALDH2 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs671 7.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001204889 ALDH2 19698717 http://www.ncbi.nlm.nih.gov/pubmed/19698717 Esophageal Neoplasms rs671 3.00E-24 Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk. NHGRI|-1
NM_001204889 ALDH2 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 gamma-Glutamyltransferase rs671 5.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001204961 PBX1 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs6670655 3.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001204963 PBX1 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs6670655 3.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_001205028 MDM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs10492304 1.68E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001205029 MDM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs10492304 1.68E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001205194 MECOM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs16852880 9.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001205206 SLC19A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9976523 7.46E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001205206 SLC19A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs9980967 2.07E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001205206 SLC19A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11701130 2.79E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001205206 SLC19A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4819143 7.47E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001205207 SLC19A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9976523 7.46E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001205207 SLC19A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs9980967 2.07E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001205207 SLC19A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11701130 2.79E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001205207 SLC19A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4819143 7.47E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001205296 TTF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1185995 1.06E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001205301 EGFLAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs2956597 9.25E-06 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_001205301 EGFLAM 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs270545 1.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_001206480 ELMO1 17653210 http://www.ncbi.nlm.nih.gov/pubmed/17653210 Diabetic Nephropathies rs741301 8.00E-06 Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population. NHGRI|-1
NM_001206480 ELMO1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs10488031 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001206480 ELMO1 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs4723619 3.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001206480 ELMO1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs6974491 2.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001206480 ELMO1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs6974491 4.00E-08 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001206480 ELMO1 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs11984075 5.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_001206482 ELMO1 17653210 http://www.ncbi.nlm.nih.gov/pubmed/17653210 Diabetic Nephropathies rs741301 8.00E-06 Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population. NHGRI|-1
NM_001206482 ELMO1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs10488031 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001206482 ELMO1 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs4723619 3.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001206482 ELMO1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs6974491 2.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001206482 ELMO1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs6974491 4.00E-08 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001206482 ELMO1 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs11984075 5.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_001206491 MAVS 20159242 http://www.ncbi.nlm.nih.gov/pubmed/20159242 Asthma rs4815617 8.00E-06 Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. NHGRI|-1
NM_001206491 MAVS 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs4815617 8.00E-08 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001206528 CRTAC1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs531676 9.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001206528 CRTAC1 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs508001 7.00E-09 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_001206540 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 2.00E-11 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001206540 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 3.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001206540 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12138950 3.00E-18 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001206540 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs10917468 1.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001206541 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 2.00E-11 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001206541 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 3.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001206541 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12138950 3.00E-18 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001206541 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs10917468 1.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_001206557 KIAA1432 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7026868 6.90E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_001206557 KIAA1432 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs4740820 6.41E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001206559 POLR1D 21471979 http://www.ncbi.nlm.nih.gov/pubmed/21471979 "Lymphoma, Large B-Cell, Diffuse" rs7097 7.00E-06 Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility. NHGRI|-1
NM_001206567 IFI16 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs1772408 8.00E-07 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_001206569 SORCS1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2245437 6.05E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001206569 SORCS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1931605 1.68E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001206569 SORCS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11592212 5.16E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001206570 SORCS1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2245437 6.05E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001206570 SORCS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1931605 1.68E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001206570 SORCS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11592212 5.16E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001206571 SORCS1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2245437 6.05E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001206571 SORCS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1931605 1.68E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001206571 SORCS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11592212 5.16E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001206572 SORCS1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2245437 6.05E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001206572 SORCS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1931605 1.68E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001206572 SORCS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11592212 5.16E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001206609 SELPLG 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs8179116 3.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001206615 EHF 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Antipsychotic Agents rs286913 7.00E-08 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001206615 EHF 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs5028798 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_001206616 EHF 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Antipsychotic Agents rs286913 7.00E-08 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_001206616 EHF 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs5028798 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_001206654 NCOR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7956328 6.36E-06 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001206654 NCOR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7956328 8.55E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001206671 RIC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4758051 2.83E-08 NBL-GWAS version 2 dbGaP|2895
NM_001206671 RIC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10840002 6.01E-06 NBL-GWAS version 2 dbGaP|2895
NM_001206672 RIC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4758051 2.83E-08 NBL-GWAS version 2 dbGaP|2895
NM_001206672 RIC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10840002 6.01E-06 NBL-GWAS version 2 dbGaP|2895
NM_001206691 RFX4 21084426 http://www.ncbi.nlm.nih.gov/pubmed/21084426 Parkinson Disease rs4964469 2.00E-07 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. NHGRI|-1
NM_001206691 RFX4 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs3891355 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_001206696 IRF6 20436469 http://www.ncbi.nlm.nih.gov/pubmed/20436469 Cleft Lip rs10863790 1.00E-14 A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. NHGRI|-1
NM_001206696 IRF6 19270707 http://www.ncbi.nlm.nih.gov/pubmed/19270707 Cleft Lip rs642961 2.00E-06 Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. NHGRI|-1
NM_001206729 AKT3 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs4132509 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001206729 AKT3 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs10927101 2.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001206729 AKT3 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs476141 1.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001206729 AKT3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1000543 1.25E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001206729 AKT3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2454222 6.14E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001206729 AKT3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2454221 8.28E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001206729 AKT3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2047137 9.15E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001206747 CAV2 20835238 http://www.ncbi.nlm.nih.gov/pubmed/20835238 "Glaucoma, Open-Angle" rs4236601 2.00E-11 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. NHGRI|-1
NM_001206748 CAV2 20835238 http://www.ncbi.nlm.nih.gov/pubmed/20835238 "Glaucoma, Open-Angle" rs4236601 2.00E-11 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. NHGRI|-1
NM_001206769 DLG2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Chemokine CCL2 rs3885683 8.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001206769 DLG2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10501570 6.75E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001206769 DLG2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10501570 7.00E-06 Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_001206769 DLG2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs6592199 1.45E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001206769 DLG2 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs1452928 7.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001206769 DLG2 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Body Height rs10898392 3.00E-06 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_001206801 RFC5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7295696 1.77E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001206804 MAP2K5 17637780 http://www.ncbi.nlm.nih.gov/pubmed/17637780 Restless Legs Syndrome rs12593813 1.00E-15 Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. NHGRI|-1
NM_001206804 MAP2K5 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2241423 1.00E-18 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001206838 PTPRZ1 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs10253361 6.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_001206839 PTPRZ1 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs10253361 6.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_001206846 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12677 3.65E-09 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001206846 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12677 5.97E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001206846 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12034362 4.45E-14 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001206846 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12034362 7.46E-13 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001206846 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2026429 6.24E-11 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001206846 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2026429 7.66E-12 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001206846 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4915337 3.65E-09 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001206846 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4915337 5.97E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001206846 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1888991 3.65E-09 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001206846 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1888991 5.97E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001206846 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6677082 3.99E-09 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001206846 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6677082 4.57E-09 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001206846 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6677082 6.47E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001206855 TFR2 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Count rs7385804 5.00E-10 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001206855 TFR2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs7385804 4.00E-10 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001206855 TFR2 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs7385804 7.00E-08 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_001206855 TFR2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7786877 3.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001206866 IL6R 19567438 http://www.ncbi.nlm.nih.gov/pubmed/19567438 C-Reactive Protein rs4537545 2.00E-14 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. NHGRI|-1
NM_001206866 IL6R 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4129267 2.00E-48 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001206866 IL6R 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Maximal Midexpiratory Flow Rate rs4129267 7.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_001206866 IL6R 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 "Receptors, Interleukin-6" rs4129267 2.00E-57 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001206866 IL6R 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs2228145 2.00E-08 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_001206866 IL6R 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs2228145 2.00E-11 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_001206880 MRVI1 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7940646 1.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001206880 MRVI1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2018368 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001206880 MRVI1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11042937 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001206881 MRVI1 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7940646 1.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_001206881 MRVI1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2018368 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001206881 MRVI1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11042937 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001206897 ALDH1A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs597804 5.59E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001206897 ALDH1A2 19609347 http://www.ncbi.nlm.nih.gov/pubmed/19609347 Hypertension rs1550576 3.00E-06 A genome-wide association study of hypertension and blood pressure in African Americans. NHGRI|-1
NM_001206920 SLC35F4 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Bipolar Disorder rs10134944 7.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001206920 SLC35F4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1092015 2.23E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001206920 SLC35F4 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs8013190 7.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001206920 SLC35F4 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs1335515 8.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_001206920 SLC35F4 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Maximal Midexpiratory Flow Rate rs808225 7.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_001206920 SLC35F4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2747100 1.13E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001206946 PICALM 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs536841 3.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_001206946 PICALM 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs561655 7.00E-11 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_001206946 PICALM 19734902 http://www.ncbi.nlm.nih.gov/pubmed/19734902 Alzheimer Disease rs3851179 1.00E-09 Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. NHGRI|-1
NM_001206947 PICALM 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs536841 3.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_001206947 PICALM 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs561655 7.00E-11 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_001206947 PICALM 19734902 http://www.ncbi.nlm.nih.gov/pubmed/19734902 Alzheimer Disease rs3851179 1.00E-09 Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. NHGRI|-1
NM_001206955 CNTN4 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs2619566 7.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001206955 CNTN4 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs4370013 4.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001206956 CNTN4 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs2619566 7.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001206956 CNTN4 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs4370013 4.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001218 CA12 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs10519210 1.00E-08 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_001221 CAMK2D 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs13134836 2.84E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001221 CAMK2D 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12331375 1.11E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001232 CASQ2 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs4074536 2.00E-08 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001233 CAV2 20835238 http://www.ncbi.nlm.nih.gov/pubmed/20835238 "Glaucoma, Open-Angle" rs4236601 2.00E-11 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. NHGRI|-1
NM_001235 SERPINH1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs634552 4.00E-13 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001238 CCNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs184583 2.90E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001238 CCNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs184583 3.72E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001238 CCNE1 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs8102137 2.00E-11 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_001240 CCNT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7297499 5.97E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001244 TNFSF8 21699788 http://www.ncbi.nlm.nih.gov/pubmed/21699788 Inflammatory Bowel Diseases rs2006996 4.00E-13 HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease. NHGRI|-1
NM_001244 TNFSF8 21699788 http://www.ncbi.nlm.nih.gov/pubmed/21699788 Inflammatory Bowel Diseases rs2006996 4.00E-16 HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease. NHGRI|-1
NM_001244 TNFSF8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs7866342 1.01E-05 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_001250 CD40 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs4810485 3.00E-09 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_001250 CD40 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 "Arthritis, Rheumatoid" rs4810485 8.00E-09 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_001250 CD40 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs6074022 1.00E-07 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_001253 CDC5L 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs13198841 8.51E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001257 CDH13 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs11646411 7.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_001257 CDH13 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs12386026 2.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_001257 CDH13 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Coronary Disease rs8055236 6.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001257 CDH13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs11150555 1.70E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001257 CDH13 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs10514585 5.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_001257 CDH13 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17216786 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001257 CDH13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4238691 5.55E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001257 CDH13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs9930750 3.14E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001257 CDH13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4357934 2.19E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001257 CDH13 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs6563943 6.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_001257 CDH13 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs3096277 1.00E-09 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001257 CDH13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2967391 1.52E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001257 CDH13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2967340 2.14E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001257 CDH13 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Bone Density rs4087296 3.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001257 CDH13 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs4082514 3.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001257 CDH13 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs1991867 4.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001257 CDH13 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Benzodiazepines rs4783227 4.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001257 CDH13 19304780 http://www.ncbi.nlm.nih.gov/pubmed/19304780 Hypertension rs11646213 8.00E-06 Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations. NHGRI|-1
NM_001257 CDH13 20887962 http://www.ncbi.nlm.nih.gov/pubmed/20887962 Adiponectin rs3865188 3.00E-83 Adiponectin concentrations: a genome-wide association study. NHGRI|-1
NM_001257 CDH13 20876611 http://www.ncbi.nlm.nih.gov/pubmed/20876611 Adiponectin rs3865188 4.00E-30 Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ. NHGRI|-1
NM_001259 CDK6 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 "Arthritis, Rheumatoid" rs42041 4.00E-06 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_001259 CDK6 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs2040494 4.00E-07 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_001259 CDK6 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs2282978 1.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001259 CDK6 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs2282978 1.00E-08 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001259 CDK6 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs2282978 8.00E-23 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_001259 CDK6 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs445 2.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001259 CDK6 21738479 http://www.ncbi.nlm.nih.gov/pubmed/21738479 Leukocyte Count rs445 4.00E-07 "Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT)." NHGRI|-1
NM_001259 CDK6 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs445 7.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001262 CDKN2C 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs17391905 3.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001264 CDSN 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130981 9.90E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001264 CDSN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111573149 1.16E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001264 CDSN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1062470 8.99E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001264 CDSN 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs3094212 7.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001270 CHD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs467728 1.33E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001276 CHI3L1 18403759 http://www.ncbi.nlm.nih.gov/pubmed/18403759 Glycoproteins rs4950928 1.00E-13 "Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function." NHGRI|-1
NM_001276 CHI3L1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6691378 3.76E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001276 CHI3L1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4950929 1.32E-12 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001276 CHI3L1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs946263 9.74E-13 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001276 CHI3L1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2153101 9.74E-13 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001286 CLCN6 21273288 http://www.ncbi.nlm.nih.gov/pubmed/21273288 "Natriuretic Peptide, Brain" rs1023252 4.00E-16 Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. NHGRI|-1
NM_001295 CCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10510749 4.22E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001295 CCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7631551 7.95E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001295 CCR1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs13098911 3.00E-17 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001297 CNGB1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs3784900 6.67E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001297 CNGB1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs3784901 5.51E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001298 CNGA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7571001 1.95E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001300 KLF6 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs6601764 9.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001300 KLF6 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs2031577 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001300 KLF6 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Mass Index rs10458787 1.00E-06 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_001300 KLF6 20662065 http://www.ncbi.nlm.nih.gov/pubmed/20662065 Lupus Vulgaris rs1391511 7.00E-06 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. NHGRI|-1
NM_001300 KLF6 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs2764980 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001300 KLF6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17135017 4.32E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001300 KLF6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11251836 2.88E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001300 KLF6 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Bone Density rs2165468 1.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001300 KLF6 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4881184 5.93E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001308 CPN1 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs11597390 2.00E-08 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_001313 CRMP1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4292278 7.31E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001317 CSH1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2665838 5.00E-25 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001320 CSNK2B 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3130618 9.99E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001322 CST2 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 "Arthritis, Rheumatoid" rs6138150 3.00E-06 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_001329 CTBP2 18264096 http://www.ncbi.nlm.nih.gov/pubmed/18264096 Prostatic Neoplasms rs4962416 2.00E-07 Multiple loci identified in a genome-wide association study of prostate cancer. NHGRI|-1
NM_001332 CTNND2 21095009 http://www.ncbi.nlm.nih.gov/pubmed/21095009 Myopia rs6885224 8.00E-06 Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese. NHGRI|-1
NM_001332 CTNND2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17176973 2.27E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_001338 CXADR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Blood Pressure rs211953 8.91E-05 Genomewide association analysis of systolic blood pressure (SBP) in a birth cohort from a founder population dbGaP|2903
NM_001340 CYLC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1867347 2.08E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001340 CYLC2 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs1342899 8.00E-07 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_001343 DAB2 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs11959928 1.00E-07 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001343 DAB2 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs2548145 2.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_001343 DAB2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs4613763 7.00E-27 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_001343 DAB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4613763 6.97E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001343 DAB2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs17234657 2.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001343 DAB2 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs11742570 7.00E-36 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001343 DAB2 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6451493 3.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001343 DAB2 17684544 http://www.ncbi.nlm.nih.gov/pubmed/17684544 Crohn Disease rs1992660 4.00E-07 Systematic association mapping identifies NELL1 as a novel IBD disease gene. NHGRI|-1
NM_001343 DAB2 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs6896969 2.00E-07 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_001343 DAB2 17447842 http://www.ncbi.nlm.nih.gov/pubmed/17447842 Crohn Disease rs1373692 2.00E-12 Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4. NHGRI|-1
NM_001343 DAB2 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs9292777 3.00E-18 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_001343 DAB2 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs10440635 3.00E-07 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_001346 DGKG 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs7647305 7.00E-11 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001346 DGKG 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7647305 4.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001346 DGKG 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs9816226 2.00E-18 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001347 DGKQ 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs11248060 2.00E-06 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_001347 DGKQ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11248060 3.39E-06 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_001348 DAPK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7255123 7.90E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001349 DARS 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs309160 2.54E-07 NBL-GWAS version 1 dbGaP|2845
NM_001349 DARS 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs309137 3.48E-07 NBL-GWAS version 1 dbGaP|2845
NM_001349 DARS 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs749873 1.79E-06 NBL-GWAS version 1 dbGaP|2845
NM_001349 DARS 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2011946 7.16E-06 NBL-GWAS version 1 dbGaP|2845
NM_001349 DARS 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs932206 1.07E-06 NBL-GWAS version 1 dbGaP|2845
NM_001364 DLG2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Chemokine CCL2 rs3885683 8.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001364 DLG2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10501570 6.75E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001364 DLG2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10501570 7.00E-06 Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_001364 DLG2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs6592199 1.45E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001364 DLG2 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs1452928 7.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001364 DLG2 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Body Height rs10898392 3.00E-06 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_001369 DNAH5 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Ankle Brachial Index rs2896103 5.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001369 DNAH5 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Ankle Brachial Index rs7715811 6.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001369 DNAH5 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Ankle Brachial Index rs1502050 9.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001373 DNAH14 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2662928 8.79E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001373 DNAH14 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs1892121 6.78E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_001376 DYNC1H1 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs4906172 3.00E-06 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_001377 DYNC2H1 21118971 http://www.ncbi.nlm.nih.gov/pubmed/21118971 Small Cell Lung Carcinoma rs716274 9.00E-08 Genome-wide interrogation identifies YAP1 variants associated with survival of small-cell lung cancer patients. NHGRI|-1
NM_001377 DYNC2H1 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs1917445 6.00E-07 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001377 DYNC2H1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs974819 2.00E-09 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_001380 DOCK1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4255455 6.99E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001389 DSCAM 21079520 http://www.ncbi.nlm.nih.gov/pubmed/21079520 "Carcinoma, Non-Small-Cell Lung" rs9981861 4.00E-06 Genome-wide association study on overall survival of advanced non-small cell lung cancer patients treated with carboplatin and paclitaxel. NHGRI|-1
NM_001389 DSCAM 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2837754 2.85E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001389 DSCAM 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3804024 2.95E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001389 DSCAM 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs2837828 1.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001389 DSCAM 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Arthritis, Rheumatoid" rs2837960 2.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001394 DUSP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs601962 5.33E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001394 DUSP4 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, HDL" rs10091038 3.00E-08 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001395 DUSP9 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs5945326 3.00E-10 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_001396 DYRK1A 21364930 http://www.ncbi.nlm.nih.gov/pubmed/21364930 HIV-1 rs12483205 5.00E-06 Genome-wide association study identifies single nucleotide polymorphism in DYRK1A associated with replication of HIV-1 in monocyte-derived macrophages. NHGRI|-1
NM_001396 DYRK1A 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs2835810 6.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_001399 EDA 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs5936487 6.00E-11 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001399 EDA 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs4844096 5.00E-11 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_001400 S1PR1 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs17410015 2.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001401 LPAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1536435 1.10E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001401 LPAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1536435 9.93E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001401 LPAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs509276 2.53E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001408 CELSR2 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs12740374 2.00E-42 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001408 CELSR2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs12740374 9.00E-29 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001408 CELSR2 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs660240 1.00E-26 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001408 CELSR2 20686565 http://www.ncbi.nlm.nih.gov/pubmed/20686565 Lipids rs629301 1.00E-170 "Biological, clinical and population relevance of 95 loci for blood lipids." NHGRI|-1
NM_001408 CELSR2 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs646776 2.00E-12 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001408 CELSR2 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs646776 3.00E-29 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_001408 CELSR2 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs646776 8.00E-23 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001408 CELSR2 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs646776 4.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001408 CELSR2 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs646776 9.00E-22 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001408 CELSR2 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs646776 6.00E-10 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_001408 CELSR2 21087763 http://www.ncbi.nlm.nih.gov/pubmed/21087763 "GRN protein, human [Supplementary Concept]" rs646776 2.00E-30 Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma. NHGRI|-1
NM_001408 CELSR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs646776 2.19E-12 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_001408 CELSR2 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs646776 8.00E-12 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_001422 ELF5 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1323690 1.74E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001422 ELF5 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs5028798 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_001424 EMP2 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs11074889 7.00E-07 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_001424 EMP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4780959 8.18E-05 NBL-GWAS version 2 dbGaP|2895
NM_001426 EN1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs13028041 1.66E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001426 EN1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs651477 2.00E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001426 EN1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs651477 7.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001430 EPAS1 21131975 http://www.ncbi.nlm.nih.gov/pubmed/21131975 "Carcinoma, Renal Cell" rs7579899 2.00E-09 Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3. NHGRI|-1
NM_001430 EPAS1 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs12623288 3.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001430 EPAS1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs2346177 2.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001432 EREG 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1350666 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_001437 ESR2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1256065 8.27E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001437 ESR2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1256059 4.61E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001437 ESR2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1256044 4.68E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001437 ESR2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1269056 5.46E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001438 ESRRG 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs12757165 1.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001438 ESRRG 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs1436900 7.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_001438 ESRRG 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs1497828 4.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001451 FOXF1 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs305061 4.00E-07 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_001451 FOXF1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs16940202 6.00E-19 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001451 FOXF1 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs17445836 4.00E-09 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_001451 FOXF1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs11117432 5.00E-11 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001451 FOXF1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs987052 8.15E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001451 FOXF1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs2696835 3.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_001451 FOXF1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, HDL" rs11641231 8.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001452 FOXF2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs9328053 4.70E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_001452 FOXF2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2745636 5.45E-06 NBL-GWAS version 1 dbGaP|2845
NM_001452 FOXF2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs6906804 3.67E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001452 FOXF2 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs9502893 3.00E-07 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_001455 FOXO3 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs9480865 7.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001455 FOXO3 21216879 http://www.ncbi.nlm.nih.gov/pubmed/21216879 Insulin-Like Growth Factor I rs2153960 5.00E-07 A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. NHGRI|-1
NM_001457 FLNB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4681795 1.70E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_001478 B4GALNT1 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs10876993 4.00E-06 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_001480 GALR1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs2717128 1.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001482 GATM 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs2453533 5.00E-22 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001486 GCKR 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Albumins rs1260326 4.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001486 GCKR 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs1260326 5.00E-40 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001486 GCKR 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs1260326 3.00E-10 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_001486 GCKR 20657596 http://www.ncbi.nlm.nih.gov/pubmed/20657596 Hypertriglyceridemia rs1260326 7.00E-09 Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. NHGRI|-1
NM_001486 GCKR 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs1260326 3.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001486 GCKR 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs1260326 2.00E-31 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001486 GCKR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs1260326 3.56E-10 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001486 GCKR 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Triglycerides rs1260326 4.00E-10 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_001486 GCKR 18454146 http://www.ncbi.nlm.nih.gov/pubmed/18454146 Triglycerides rs1260326 4.00E-08 Common genetic variation near MC4R is associated with waist circumference and insulin resistance. NHGRI|-1
NM_001486 GCKR 18179892 http://www.ncbi.nlm.nih.gov/pubmed/18179892 "Cholesterol, LDL" rs780094 5.00E-07 Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. NHGRI|-1
NM_001486 GCKR 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs780094 7.00E-15 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_001486 GCKR 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs780094 6.00E-38 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001486 GCKR 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs780094 4.00E-20 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001486 GCKR 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Insulin Resistance rs780094 3.00E-24 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_001486 GCKR 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs780094 3.00E-14 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_001486 GCKR 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Triglycerides rs780094 3.00E-20 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001486 GCKR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs780094 5.03E-09 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_001486 GCKR 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs780094 6.00E-32 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001486 GCKR 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs780094 1.00E-09 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_001486 GCKR 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs780093 7.00E-06 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_001486 GCKR 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs780093 5.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001486 GCKR 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs780093 2.00E-12 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001486 GCKR 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs780093 3.00E-10 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001486 GCKR 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs780093 4.00E-17 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_001486 GCKR 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs1260333 2.00E-19 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001490 GCNT1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs6560517 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001494 GDI2 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2380205 5.00E-07 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001500 GMDS 21502949 http://www.ncbi.nlm.nih.gov/pubmed/21502949 Caudate Nucleus rs9378688 6.00E-06 Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search. NHGRI|-1
NM_001500 GMDS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6911560 1.79E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001502 GP2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs12444268 2.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001502 GP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6497465 5.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001502 GP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs8054898 5.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001503 GPLD1 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs9467160 1.00E-11 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_001508 GPR39 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs16831128 4.00E-07 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001508 GPR39 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs16831128 5.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_001526 HCRTR2 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs9367630 1.00E-07 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001530 HIF1A 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 CD40 Ligand rs8005745 4.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001532 SLC29A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs7935572 1.99E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001539 DNAJA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10813923 1.61E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001539 DNAJA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10758179 1.40E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001540 HSPB1 21654844 http://www.ncbi.nlm.nih.gov/pubmed/21654844 Multiple Sclerosis rs7789940 6.00E-06 Genome-wide association study of severity in multiple sclerosis. NHGRI|-1
NM_001540 HSPB1 21654844 http://www.ncbi.nlm.nih.gov/pubmed/21654844 Multiple Sclerosis rs758944 8.00E-06 Genome-wide association study of severity in multiple sclerosis. NHGRI|-1
NM_001544 ICAM4 18604267 http://www.ncbi.nlm.nih.gov/pubmed/18604267 Intercellular Adhesion Molecule-1 rs5498 5.00E-25 "Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women." NHGRI|-1
NM_001544 ICAM4 21533024 http://www.ncbi.nlm.nih.gov/pubmed/21533024 Intercellular Adhesion Molecule-1 rs5498 6.00E-89 "Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci." NHGRI|-1
NM_001544 ICAM4 18604267 http://www.ncbi.nlm.nih.gov/pubmed/18604267 Intercellular Adhesion Molecule-1 rs281437 3.00E-10 "Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women." NHGRI|-1
NM_001544 ICAM4 20167578 http://www.ncbi.nlm.nih.gov/pubmed/20167578 Intercellular Adhesion Molecule-1 rs3093030 4.00E-23 Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. NHGRI|-1
NM_001546 ID4 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs16883019 7.00E-07 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001546 ID4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17483277 7.61E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001550 IFRD1 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs17159640 9.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_001557 CXCR2 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs11676348 1.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001559 IL12RB2 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs17129789 9.00E-20 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001559 IL12RB2 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs3790567 3.00E-11 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_001559 IL12RB2 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs3790567 8.00E-12 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_001559 IL12RB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs7539328 1.10E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001559 IL12RB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11209032 8.65E-10 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001559 IL12RB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1495966 6.09E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001559 IL12RB2 20622879 http://www.ncbi.nlm.nih.gov/pubmed/20622879 Behcet Syndrome rs1495965 2.00E-11 Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behtet's disease susceptibility loci. NHGRI|-1
NM_001559 IL12RB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1495965 6.99E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001559 IL12RB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1495965 1.51E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001559 IL12RB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs924080 5.35E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001559 IL12RB2 20622878 http://www.ncbi.nlm.nih.gov/pubmed/20622878 Behcet Syndrome rs924080 7.00E-09 "Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behtet's disease." NHGRI|-1
NM_001559 IL12RB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs924080 2.57E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001562 IL18 20150558 http://www.ncbi.nlm.nih.gov/pubmed/20150558 Interleukin-18 rs1834481 1.00E-08 Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels. NHGRI|-1
NM_001584 MPPED2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2593549 9.26E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001584 MPPED2 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs3925584 5.00E-16 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_001608 ACADL 20037589 http://www.ncbi.nlm.nih.gov/pubmed/20037589 Nonalcoholic Fatty Liver Disease rs2286963 3.00E-60 A genome-wide perspective of genetic variation in human metabolism. NHGRI|-1
NM_001611 ACP5 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs7253363 9.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001613 ACTA2 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs1926203 1.00E-06 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_001621 AHR 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs10499504 4.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_001621 AHR 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs4410790 2.00E-19 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_001621 AHR 21357676 http://www.ncbi.nlm.nih.gov/pubmed/21357676 Coffee rs6968865 2.00E-11 Sequence variants at CYP1A1-CYP1A2 and AHR associate with coffee consumption. NHGRI|-1
NM_001623 AIF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2269475 4.48E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001623 AIF1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2736177 3.15E-23 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001624 AIM1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs783396 9.24E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001624 AIM1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs783396 9.00E-06 A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. NHGRI|-1
NM_001624 AIM1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs6568433 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001624 AIM1 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Atrial Natriuretic Factor rs1417352 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_001635 AMPH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6967370 5.10E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001637 AOAH 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs6948404 3.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_001637 AOAH 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs17329669 9.82E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_001638 APOF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11575221 5.71E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001640 APEH 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs9822268 2.00E-17 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001645 APOC1 20442857 http://www.ncbi.nlm.nih.gov/pubmed/20442857 1-Alkyl-2-acetylglycerophosphocholine Esterase rs4420638 6.00E-24 Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study. NHGRI|-1
NM_001645 APOC1 17474819 http://www.ncbi.nlm.nih.gov/pubmed/17474819 Alzheimer Disease rs4420638 1.00E-39 A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease. NHGRI|-1
NM_001645 APOC1 17975299 http://www.ncbi.nlm.nih.gov/pubmed/17975299 Alzheimer Disease rs4420638 1.00E-39 Sorl1 as an Alzheimer's disease predisposition gene? NHGRI|-1
NM_001645 APOC1 17998437 http://www.ncbi.nlm.nih.gov/pubmed/17998437 Alzheimer Disease rs4420638 2.00E-44 Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease. NHGRI|-1
NM_001645 APOC1 18262040 http://www.ncbi.nlm.nih.gov/pubmed/18262040 "Cholesterol, LDL" rs4420638 1.00E-20 LDL-cholesterol concentrations: a genome-wide association study. NHGRI|-1
NM_001645 APOC1 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs4420638 1.00E-60 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_001645 APOC1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs4420638 2.00E-40 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_001645 APOC1 18802019 http://www.ncbi.nlm.nih.gov/pubmed/18802019 "Cholesterol, LDL" rs4420638 2.00E-07 Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. NHGRI|-1
NM_001645 APOC1 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Cholesterol, LDL" rs4420638 3.00E-13 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_001645 APOC1 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs4420638 3.00E-43 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001645 APOC1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs4420638 4.00E-27 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001645 APOC1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Cholesterol rs4420638 3.00E-07 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001645 APOC1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 C-Reactive Protein rs4420638 2.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001645 APOC1 21196492 http://www.ncbi.nlm.nih.gov/pubmed/21196492 C-Reactive Protein rs4420638 3.00E-07 Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus. NHGRI|-1
NM_001645 APOC1 19567438 http://www.ncbi.nlm.nih.gov/pubmed/19567438 C-Reactive Protein rs4420638 5.00E-27 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. NHGRI|-1
NM_001645 APOC1 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4420638 9.00E-139 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001645 APOC1 21740922 http://www.ncbi.nlm.nih.gov/pubmed/21740922 Longevity rs4420638 2.00E-16 A genome-wide association study confirms APOE as the major gene influencing survival in long-lived individuals. NHGRI|-1
NM_001645 APOC1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Triglycerides rs4420638 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001645 APOC1 21123754 http://www.ncbi.nlm.nih.gov/pubmed/21123754 Alzheimer Disease rs439401 1.00E-06 "Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort." NHGRI|-1
NM_001645 APOC1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs439401 1.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_001645 APOC1 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Triglycerides rs439401 2.00E-09 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001645 APOC1 20838585 http://www.ncbi.nlm.nih.gov/pubmed/20838585 Cardiovascular Diseases rs445925 9.00E-19 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. NHGRI|-1
NM_001648 KLK3 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs17632542 3.00E-46 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001648 KLK3 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs2735839 2.00E-18 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_001648 KLK3 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs266849 6.00E-10 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_001650 AQP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs9653034 3.06E-05 NBL-GWAS version 2 dbGaP|2895
NM_001650 AQP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs8083994 2.35E-05 NBL-GWAS version 2 dbGaP|2895
NM_001676 ATP12A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2862909 1.03E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001677 ATP1B1 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs10919071 1.00E-15 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001678 ATP1B2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1642763 1.61E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_001681 ATP2A2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Alpha-Globulins rs11065611 1.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001682 ATP2B1 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs2681472 1.00E-09 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001682 ATP2B1 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs2681472 2.00E-11 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001682 ATP2B1 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs2681492 4.00E-11 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_001682 ATP2B1 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Blood Pressure rs17249754 1.00E-07 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001682 ATP2B1 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs17249754 2.00E-13 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_001682 ATP2B1 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Blood Pressure rs17249754 3.00E-06 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_001682 ATP2B1 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs17249754 8.00E-20 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_001683 ATP2B2 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Phenylalanine rs6807064 1.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_001683 ATP2B2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs12632101 2.55E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001688 ATP5F1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1264898 9.33E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001688 ATP5F1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1264897 1.01E-04 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001693 ATP6V1B2 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs1106634 7.00E-07 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_001693 ATP6V1B2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs1106634 4.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001696 ATP6V1E1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9604779 5.29E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001698 AUH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10991892 2.37E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001698 AUH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs10991892 8.01E-04 Genome-wide association between genotype and incident myocardial infarction in African-American participants dbGaP|2883
NM_001698 AUH 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic Nephropathies rs773506 6.00E-06 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_001704 BAI3 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs3757057 4.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001704 BAI3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2094596 1.83E-05 NBL-GWAS version 2 dbGaP|2895
NM_001704 BAI3 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs11970254 6.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001704 BAI3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9351629 6.08E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001704 BAI3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1565488 1.10E-04 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001706 BCL6 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Blood Urea Nitrogen rs9820070 1.00E-11 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001707 BCL7B 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs13233571 4.00E-09 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001709 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001709 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001709 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_001709 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001710 CFB 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs641153 2.00E-20 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_001710 CFB 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs641153 6.00E-31 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_001710 CFB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs512559 4.99E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001710 CFB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs541862 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001710 CFB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs541862 3.41E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001710 CFB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs541862 3.78E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001710 CFB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs541862 8.34E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001710 CFB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1270942 4.69E-86 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_001710 CFB 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1270942 1.29E-17 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001710 CFB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1270942 7.82E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001710 CFB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2072633 1.47E-10 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_001710 CFB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4151672 1.74E-09 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001710 CFB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4151672 6.10E-10 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001714 BICD1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs10844154 4.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_001714 BICD1 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs10844154 6.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_001714 BICD1 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs708224 3.00E-07 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_001714 BICD1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs261902 4.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001715 BLK 19165918 http://www.ncbi.nlm.nih.gov/pubmed/19165918 "Lupus Erythematosus, Systemic" rs2618476 2.00E-08 Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. NHGRI|-1
NM_001715 BLK 21452313 http://www.ncbi.nlm.nih.gov/pubmed/21452313 "Arthritis, Rheumatoid" rs1600249 5.00E-06 Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci. NHGRI|-1
NM_001715 BLK 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs7812879 2.00E-24 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_001715 BLK 19503088 http://www.ncbi.nlm.nih.gov/pubmed/19503088 "Arthritis, Rheumatoid" rs2736340 6.00E-09 "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis." NHGRI|-1
NM_001715 BLK 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs2736340 3.00E-07 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_001715 BLK 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs13277113 1.00E-10 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_001716 CXCR5 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs6421571 3.00E-12 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001718 BMP6 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs12198986 2.00E-11 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001719 BMP7 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Eosinophils rs331615 9.00E-07 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_001719 BMP7 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs6127921 1.00E-06 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_001719 BMP7 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs6127921 3.00E-06 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_001723 DST 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12663282 4.56E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001723 DST 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9475671 1.07E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_001724 BPGM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12539126 8.96E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001724 BPGM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10488456 6.08E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_001725 BPI 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs6024905 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001730 KLF5 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12869881 5.44E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001731 BTG1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10777317 5.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001731 BTG1 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Cholesterol rs10777332 5.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001731 BTG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11106325 1.82E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001731 BTG1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs17019682 2.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_001731 BTG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4356270 4.44E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001731 BTG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4499040 6.57E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001731 BTG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11106345 6.02E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001732 BTN1A1 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs13194984 6.00E-08 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_001732 BTN1A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9358946 1.12E-08 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001732 BTN1A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs16891725 6.05E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001737 C9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4957473 4.24E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001743 CALM2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs815815 7.00E-07 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_001744 CAMK4 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs10491334 4.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001744 CAMK4 21612516 http://www.ncbi.nlm.nih.gov/pubmed/21612516 Longevity rs10491334 2.00E-06 Association Study on Long-Living Individuals from Southern Italy Identifies rs10491334 in the CAMKIV Gene That Regulates Survival Proteins. NHGRI|-1
NM_001751 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs729662 8.52E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001751 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7481584 9.54E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001751 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001751 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 4.55E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001751 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 7.54E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001751 CARS 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs739401 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001751 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs438384 1.07E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001751 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 2.60E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_001751 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 3.06E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001751 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 9.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001751 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs369461 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_001751 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs369461 7.87E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_001753 CAV1 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs3807989 4.00E-28 Genome-wide association study of PR interval. NHGRI|-1
NM_001753 CAV1 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3807989 7.00E-13 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001753 CAV1 20835238 http://www.ncbi.nlm.nih.gov/pubmed/20835238 "Glaucoma, Open-Angle" rs4236601 2.00E-11 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. NHGRI|-1
NM_001754 RUNX1 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs2014300 8.00E-22 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001759 CCND2 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs10849033 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_001759 CCND2 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Count rs11611647 6.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001760 CCND3 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Count rs3218097 1.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001760 CCND3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9349205 1.00E-31 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001760 CCND3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9349205 8.00E-20 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001760 CCND3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs11970772 7.00E-19 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_001760 CCND3 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs11968166 8.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_001771 CD22 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4805119 7.57E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001772 CD33 18976728 http://www.ncbi.nlm.nih.gov/pubmed/18976728 Alzheimer Disease rs3826656 6.00E-06 Genome-wide association analysis reveals putative Alzheimer's disease susceptibility loci in addition to APOE. NHGRI|-1
NM_001772 CD33 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs3865444 2.00E-09 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_001773 CD34 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs2745967 7.00E-08 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_001775 CD38 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs11724635 1.00E-16 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001775 CD38 21084426 http://www.ncbi.nlm.nih.gov/pubmed/21084426 Parkinson Disease rs4698412 2.00E-06 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. NHGRI|-1
NM_001775 CD38 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson Disease rs4538475 3.00E-09 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_001779 CD58 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs1335532 1.00E-07 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_001779 CD58 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs2300747 3.00E-10 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_001779 CD58 21244703 http://www.ncbi.nlm.nih.gov/pubmed/21244703 Multiple Sclerosis rs12025416 1.00E-07 Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data. NHGRI|-1
NM_001781 CD69 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs4763879 2.00E-11 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001784 CD97 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs4528684 1.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_001786 CDK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4132554 7.66E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_001791 CDC42 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2473323 3.13E-09 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_001792 CDH2 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs11083271 8.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001792 CDH2 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs4131805 2.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_001793 CDH3 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6499188 4.00E-08 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001794 CDH4 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs1970546 4.00E-08 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_001794 CDH4 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4468878 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001794 CDH4 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs2024714 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_001794 CDH4 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs944260 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001794 CDH4 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1150438 1.10E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001794 CDH4 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs6027755 6.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001795 CDH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7204297 1.86E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001796 CDH8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs3784847 1.66E-09 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001796 CDH8 21602797 http://www.ncbi.nlm.nih.gov/pubmed/21602797 Cystic Fibrosis rs11645366 7.00E-06 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. NHGRI|-1
NM_001796 CDH8 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Survival rs2639889 9.00E-07 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_001797 CDH11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7204297 1.86E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001797 CDH11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9932227 1.31E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001797 CDH11 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs1381102 6.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001805 CEBPE 19684604 http://www.ncbi.nlm.nih.gov/pubmed/19684604 "Leukemia, Lymphoid" rs2239633 3.00E-07 "Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia." NHGRI|-1
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1497430 1.31E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1497430 7.12E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs190255 1.58E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs190255 7.60E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs355464 1.30E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs355464 6.48E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11250 6.78E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs355461 1.17E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs355461 6.05E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs355506 1.17E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs355506 6.05E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs355477 4.11E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs355477 8.22E-06 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001812 CENPC1 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs1155865 2.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_001812 CENPC1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs10518025 4.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7681618 1.98E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11946612 1.31E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11946612 7.12E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs9312181 1.47E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_001812 CENPC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs9312181 7.71E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001813 CENPE 19483681 http://www.ncbi.nlm.nih.gov/pubmed/19483681 Testicular Neoplasms rs4699052 2.00E-07 A genome-wide association study of testicular germ cell tumor. NHGRI|-1
NM_001814 CTSC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17754282 4.30E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001827 CKS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13294002 7.20E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001830 CLCN4 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs12388359 4.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_001831 CLU 19734902 http://www.ncbi.nlm.nih.gov/pubmed/19734902 Alzheimer Disease rs11136000 9.00E-10 Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. NHGRI|-1
NM_001831 CLU 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs11136000 3.50E-04 Genome-wide association between genotype and incident heart failure in African-American participants dbGaP|2885
NM_001831 CLU 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs1532278 8.00E-08 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_001831 CLU 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs569214 4.00E-08 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_001831 CLU 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs17466684 7.00E-07 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_001837 CCR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9990343 2.76E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001837 CCR3 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs9990343 4.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001837 CCR3 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs6441961 3.00E-07 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_001838 CCR7 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs7221109 1.00E-09 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001843 CNTN1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Alkaline Phosphatase rs1880887 1.00E-10 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001844 COL2A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1793949 3.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001845 COL4A1 20031579 http://www.ncbi.nlm.nih.gov/pubmed/20031579 Mental Disorders rs3742207 5.00E-08 COL4A1 is associated with arterial stiffness by genome-wide association scan. NHGRI|-1
NM_001845 COL4A1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs562992 3.36E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_001845 COL4A1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs4773144 4.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001845 COL4A1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4773094 7.81E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001846 COL4A2 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs4773144 4.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001846 COL4A2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs7319311 4.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001848 COL6A1 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs4293630 7.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_001849 COL6A2 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs4293630 7.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_001850 COL8A1 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs13095226 3.00E-06 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_001850 COL8A1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs2670321 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_001850 COL8A1 20686651 http://www.ncbi.nlm.nih.gov/pubmed/20686651 Cornea rs13070584 2.00E-06 Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases. NHGRI|-1
NM_001854 COL11A1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1415363 5.62E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_001854 COL11A1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Fibrinogen rs10874639 3.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001868 CPA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs12706927 1.42E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_001875 CPS1 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Creatinine rs1047891 1.00E-15 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001875 CPS1 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs1047891 9.00E-09 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_001875 CPS1 20154341 http://www.ncbi.nlm.nih.gov/pubmed/20154341 Homocysteine rs1047891 5.00E-09 Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults. NHGRI|-1
NM_001877 CR2 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs17045328 7.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_001881 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001881 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001881 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001881 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001881 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001882 CRHBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs3792738 2.19E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001884 HAPLN1 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Prostatic Neoplasms rs4466137 3.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001884 HAPLN1 20516156 http://www.ncbi.nlm.nih.gov/pubmed/20516156 "Depressive Disorder, Major" rs310501 7.00E-06 Genome-wide association study of major recurrent depression in the U.K. population. NHGRI|-1
NM_001892 CSNK1A1 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs10058728 5.00E-09 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_001892 CSNK1A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17796714 1.02E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001900 CST5 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 "Arthritis, Rheumatoid" rs6138150 3.00E-06 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_001902 CTH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001902 CTH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 8.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_001902 CTH 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs10458561 4.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NM_001906 CTRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8056814 2.82E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001906 CTRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8056814 4.82E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001906 CTRB1 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs7202877 3.00E-15 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001906 CTRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7202877 3.59E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_001913 CUX1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2906724 3.94E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_001913 CUX1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11974778 8.09E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_001914 CYB5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10514115 6.18E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001918 DBT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11166412 2.16E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001918 DBT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4143055 2.54E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001920 DCN 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10777317 5.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_001920 DCN 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Cholesterol rs10777332 5.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001920 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11106325 1.82E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001920 DCN 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs17019682 2.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_001920 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4356270 4.44E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001920 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4499040 6.57E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001920 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11106345 6.02E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_001936 DPP6 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs6464375 4.00E-07 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_001936 DPP6 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10260404 3.00E-06 A genome-wide association study of sporadic ALS in a homogenous Irish population. NHGRI|-1
NM_001936 DPP6 18987618 http://www.ncbi.nlm.nih.gov/pubmed/18987618 Amyotrophic Lateral Sclerosis rs10260404 3.00E-06 Screening for replication of genome-wide SNP associations in sporadic ALS. NHGRI|-1
NM_001936 DPP6 18084291 http://www.ncbi.nlm.nih.gov/pubmed/18084291 Amyotrophic Lateral Sclerosis rs10260404 5.00E-08 Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis. NHGRI|-1
NM_001936 DPP6 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6952728 5.15E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001937 DPT 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Survival rs1412337 2.00E-09 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_001941 DSC3 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Parathyroid Hormone rs2729409 3.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001942 DSG1 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs7236477 7.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_001944 DSG3 19772629 http://www.ncbi.nlm.nih.gov/pubmed/19772629 Parkinson Disease rs1941184 4.00E-06 Genomewide association study for onset age in Parkinson disease. NHGRI|-1
NM_001948 DUT 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Adiponectin rs11637235 3.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001950 E2F4 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs3729639 2.00E-11 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001953 TYMP 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs470119 4.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264327 1.68E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2239518 3.45E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9468843 9.01E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3129975 2.40E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs12526186 1.27E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001954 DDR1 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs12526186 3.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001954 DDR1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs6911628 2.20E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs4711229 5.43E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs3131043 1.76E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3131043 1.81E-11 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs34682678 1.68E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9295917 5.09E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs13198118 2.07E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264362 1.31E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001954 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs886424 4.70E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9295924 2.69E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs4713380 6.51E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs915664 8.45E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001954 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1264350 1.86E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7749924 2.25E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2535331 3.74E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2250264 8.16E-09 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001954 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2844659 1.23E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2535327 1.30E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844654 4.43E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264333 4.42E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264332 4.98E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264331 4.47E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_001954 DDR1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs7756521 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001954 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7756521 7.58E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_001955 EDN1 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs1040994 2.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_001962 EFNA5 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs252817 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001962 EFNA5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6888194 1.66E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001962 EFNA5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12519552 5.73E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001962 EFNA5 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs10074258 2.00E-07 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_001962 EFNA5 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs7447447 7.00E-06 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_001962 EFNA5 21368711 http://www.ncbi.nlm.nih.gov/pubmed/21368711 Social Desirability rs10479334 2.00E-09 Genome-wide association study of personality traits in bipolar patients. NHGRI|-1
NM_001963 EGF 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs9685587 6.63E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_001963 EGF 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs17316633 9.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_001966 EHHADH 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs7374394 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_001966 EHHADH 21042317 http://www.ncbi.nlm.nih.gov/pubmed/21042317 "Depressive Disorder, Major" rs7647854 5.00E-06 "Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned." NHGRI|-1
NM_001977 ENPEP 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs244040 3.71E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_001977 ENPEP 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs6825911 7.00E-08 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_001977 ENPEP 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs6825911 9.00E-09 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_001982 ERBB3 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs2292239 2.00E-20 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_001982 ERBB3 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2292239 2.00E-25 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001982 ERBB3 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs2292239 3.00E-16 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_001982 ERBB3 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs12580100 1.00E-06 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_001982 ERBB3 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs11171739 1.00E-11 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_001987 ETV6 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs2187642 2.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001987 ETV6 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2856321 5.00E-15 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001987 ETV6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2856336 7.69E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001987 ETV6 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2710287 7.55E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_001987 ETV6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10505762 1.72E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_001993 F3 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs12029080 6.00E-52 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10754210 1.56E-14 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10754210 7.22E-14 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2990510 4.24E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2990510 4.80E-06 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2990510 9.94E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6003 2.53E-10 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6003 3.65E-09 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6003 4.16E-11 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6003 5.97E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1759006 6.06E-09 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1412632 1.42E-08 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1412632 9.67E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1412631 2.17E-09 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1412631 4.76E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6663083 2.70E-17 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6663083 5.47E-12 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7555070 5.60E-22 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7555070 5.69E-24 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1332666 1.19E-50 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_001994 F13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1332666 3.74E-45 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_001998 FBLN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17793957 1.85E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_001998 FBLN2 21368711 http://www.ncbi.nlm.nih.gov/pubmed/21368711 Personality rs9846232 1.00E-08 Genome-wide association study of personality traits in bipolar patients. NHGRI|-1
NM_001999 FBN2 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs374748 4.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_001999 FBN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12523161 9.20E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002001 FCER1A 18846228 http://www.ncbi.nlm.nih.gov/pubmed/18846228 Immunoglobulin E rs2251746 2.00E-20 Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus. NHGRI|-1
NM_002001 FCER1A 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Chemokine CCL2 rs2494250 1.00E-14 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_002009 FGF7 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs4338740 1.00E-12 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_002009 FGF7 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs4338740 3.00E-13 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_002010 FGF9 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Dibenzothiazepines rs518590 2.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_002010 FGF9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs9316567 6.58E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_002010 FGF9 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Interleukin 1 Receptor Antagonist Protein rs17369571 1.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_002010 FGF9 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs7318731 1.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_002010 FGF9 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs1034200 4.00E-09 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_002012 FHIT 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs1825630 8.00E-06 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_002012 FHIT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs3912494 9.80E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_002012 FHIT 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs10510837 4.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_002012 FHIT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1735460 3.40E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_002012 FHIT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1735460 3.67E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_002012 FHIT 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs6791644 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_002012 FHIT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9825823 2.13E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_002012 FHIT 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs10514718 4.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_002012 FHIT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2121794 2.14E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_002015 FOXO1 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs9548988 3.00E-07 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_002015 FOXO1 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Alanine Transaminase rs10492681 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_002015 FOXO1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs941823 4.00E-12 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_002015 FOXO1 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs2755237 1.00E-08 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_002015 FOXO1 20485516 http://www.ncbi.nlm.nih.gov/pubmed/20485516 Cornea rs2721051 5.00E-10 Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. NHGRI|-1
NM_002016 FLG 21666691 http://www.ncbi.nlm.nih.gov/pubmed/21666691 "Dermatitis, Atopic" rs3126085 6.00E-12 Genome-wide association study identifies two new susceptibility loci for atopic dermatitis in the Chinese Han population. NHGRI|-1
NM_002016 FLG 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Exploratory Behavior rs3120665 4.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_002017 FLI1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs588407 3.45E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_002019 FLT1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs17086609 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_002020 FLT4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2387207 4.50E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_002021 FMO1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10798304 6.73E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_002021 FMO1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs6660565 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_002022 FMO4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10798304 6.73E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_002022 FMO4 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs6660565 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_002023 FMOD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6428009 6.92E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_002025 AFF2 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs5936441 5.00E-06 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_002025 AFF2 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs2159767 7.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_002026 FN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1250255 3.21E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_002028 FNTB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4466998 5.00E-08 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_002031 FRK 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs9488363 2.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_002036 DARC 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs2814778 1.00E-08 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_002036 DARC 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Chemokine CCL2 rs10489849 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_002043 GABRR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4707535 5.97E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_002043 GABRR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2325202 2.65E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_002045 GAP43 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4831199 1.07E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_002045 GAP43 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11926976 7.10E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_002051 GATA3 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs10508343 8.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_002054 GCG 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 "Ear, External" rs2270447 8.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_002059 GH2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2665838 5.00E-25 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_002063 GLRA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs3020867 1.46E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_002068 GNA15 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs11880198 6.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_002068 GNA15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs11880198 7.10E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_002071 GNAL 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10468679 1.72E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_002079 GOT1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs4409764 2.00E-20 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_002079 GOT1 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs10883365 4.00E-10 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_002079 GOT1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs10883365 6.00E-08 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_002079 GOT1 20228798 http://www.ncbi.nlm.nih.gov/pubmed/20228798 "Colitis, Ulcerative" rs6584283 2.00E-06 Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). NHGRI|-1
NM_002079 GOT1 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs6584283 2.00E-07 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_002079 GOT1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6584283 8.00E-21 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_002080 GOT2 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs12600277 3.00E-06 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_002081 GPC1 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs1574192 4.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_002082 GRK6 21546496 http://www.ncbi.nlm.nih.gov/pubmed/21546496 Blood Platelets rs2731672 1.00E-06 Novel loci involved on platelet function and platelet count identified by a genome-wide study performed in children. NHGRI|-1
NM_002082 GRK6 20303064 http://www.ncbi.nlm.nih.gov/pubmed/20303064 Partial Thromboplastin Time rs2731672 2.00E-30 "Common variants of large effect in F12, KNG1, and HRG are associated with activated partial thromboplastin time." NHGRI|-1
NM_002086 GRB2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs16967789 1.10E-06 NBL-GWAS version 1 dbGaP|2845
NM_002086 GRB2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs9892996 2.23E-07 NBL-GWAS version 1 dbGaP|2845
NM_002089 CXCL2 21738479 http://www.ncbi.nlm.nih.gov/pubmed/21738479 Leukocyte Count rs1371799 2.00E-17 "Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT)." NHGRI|-1
NM_002089 CXCL2 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs546829 3.00E-07 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_002091 GRP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9961404 1.02E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_002091 GRP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1517037 6.81E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_002091 GRP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9319943 3.34E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_002097 GTF3A 17903306 http://www.ncbi.nlm.nih.gov/pubmed/17903306 Electrocardiography rs10507380 8.00E-06 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. NHGRI|-1
NM_002097 GTF3A 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs9512637 1.00E-07 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_002099 GYPA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7690204 5.83E-06 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_002099 GYPA 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs12504628 6.00E-13 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_002099 GYPA 19300500 http://www.ncbi.nlm.nih.gov/pubmed/19300500 Respiratory Function Tests rs13147758 8.00E-11 A genome-wide association study of pulmonary function measures in the Framingham Heart Study. NHGRI|-1
NM_002099 GYPA 19300482 http://www.ncbi.nlm.nih.gov/pubmed/19300482 "Pulmonary Disease, Chronic Obstructive" rs1828591 1.00E-07 A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci. NHGRI|-1
NM_002099 GYPA 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs1980057 3.00E-20 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_002099 GYPA 20173748 http://www.ncbi.nlm.nih.gov/pubmed/20173748 "Pulmonary Disease, Chronic Obstructive" rs13118928 5.00E-07 Variants in FAM13A are associated with chronic obstructive pulmonary disease. NHGRI|-1
NM_002101 GYPC 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs13418717 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_002101 GYPC 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6710520 2.18E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_002101 GYPC 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10207651 7.81E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_002113 CFHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922144 1.53E-32 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002113 CFHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922144 3.90E-37 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_002113 CFHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6657442 1.30E-38 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_002113 CFHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6657442 2.07E-33 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002113 CFHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7517126 5.99E-20 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002113 CFHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs13375144 5.05E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002113 CFHR1 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs6428370 7.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_002113 CFHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801575 1.13E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002113 CFHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801575 7.31E-11 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_002113 CFHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801575 8.31E-14 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_002114 HIVEP1 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs1040994 2.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_002114 HIVEP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs6457906 5.45E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_002116 HLA-A 21428769 http://www.ncbi.nlm.nih.gov/pubmed/21428769 Carbamazepine rs1061235 1.00E-07 HLA-A*3101 and carbamazepine-induced hypersensitivity reactions in Europeans. NHGRI|-1
NM_002116 HLA-A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113803590 3.89E-10 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002116 HLA-A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111378352 3.90E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2853950 1.76E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2395471 8.84E-18 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2249741 3.34E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2249742 6.35E-18 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7773175 4.77E-30 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs7759127 1.50E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002117 HLA-C 20953186 http://www.ncbi.nlm.nih.gov/pubmed/20953186 "Arthritis, Psoriatic" rs13191343 2.00E-72 Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. NHGRI|-1
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2524082 2.22E-11 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3132486 6.12E-79 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3132486 6.66E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3132485 2.62E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111614996 7.62E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2524073 2.71E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2524070 1.97E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2524068 2.40E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002117 HLA-C 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs7382297 5.05E-14 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4446605 1.42E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2894181 4.06E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3887152 7.09E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111842959 1.03E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130952 3.34E-14 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9263948 8.67E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9468898 2.51E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113433663 1.79E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112560858 2.67E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112499718 3.17E-10 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9263967 7.30E-15 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3130467 5.92E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3130467 1.34E-27 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113031990 1.72E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3130517 1.43E-28 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3130473 1.86E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3130713 9.81E-28 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3130685 8.58E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2394895 2.59E-29 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3095250 2.89E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130532 4.33E-12 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3132496 2.90E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3130425 1.81E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4084090 2.86E-09 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs3095254 6.00E-11 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2844627 2.31E-36 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111453581 2.06E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002117 HLA-C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113198053 1.61E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002118 HLA-DMB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs151719 2.63E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002118 HLA-DMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs241403 1.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_002118 HLA-DMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3101942 3.09E-110 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002118 HLA-DMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs3101942 6.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_002118 HLA-DMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs154981 3.14E-91 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002118 HLA-DMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs154978 4.49E-81 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs11244 1.20E-102 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs11575907 5.96E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2071474 6.65E-70 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2071472 1.89E-69 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2071554 9.90E-81 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2071554 2.30E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2071469 1.32E-84 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1894406 9.40E-88 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2857106 2.39E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9784758 6.79E-77 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9784758 2.30E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002120 HLA-DOB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6902723 8.63E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs6903130 6.43E-72 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs6903130 4.43E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002120 HLA-DOB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6903130 1.70E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002120 HLA-DOB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9296044 2.95E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs6901084 1.21E-85 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9368741 3.26E-95 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2857210 4.10E-14 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9276644 2.04E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7762279 2.40E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_002120 HLA-DOB 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs7762279 2.97E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002120 HLA-DOB 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs7758736 1.15E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7758736 3.07E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_002120 HLA-DOB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2621384 4.64E-14 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002120 HLA-DOB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2857161 8.19E-14 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002120 HLA-DOB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2621383 9.05E-14 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002120 HLA-DOB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2621382 3.11E-10 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002120 HLA-DOB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2157082 1.34E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002120 HLA-DOB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2857154 6.68E-12 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9276726 1.28E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs7767167 9.33E-68 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2219893 2.56E-68 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002120 HLA-DOB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2857136 4.56E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002120 HLA-DOB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2857129 3.53E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002121 HLA-DPB1 19349983 http://www.ncbi.nlm.nih.gov/pubmed/19349983 Hepatitis B rs9277535 6.00E-39 A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians. NHGRI|-1
NM_002122 HLA-DQA1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs9272346 5.00E-134 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_002122 HLA-DQA1 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs9272346 6.00E-129 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_002122 HLA-DQA1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9272346 8.87E-12 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002122 HLA-DQA1 17558408 http://www.ncbi.nlm.nih.gov/pubmed/17558408 Celiac Disease rs2187668 1.00E-19 A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21. NHGRI|-1
NM_002122 HLA-DQA1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs2187668 1.00E-50 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_002122 HLA-DQA1 21323541 http://www.ncbi.nlm.nih.gov/pubmed/21323541 "Glomerulonephritis, Membranous" rs2187668 8.00E-93 Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy. NHGRI|-1
NM_002122 HLA-DQA1 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs2187668 2.00E-33 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_002122 HLA-DQA1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2187668 2.71E-21 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002122 HLA-DQA1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2187668 3.00E-21 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_002122 HLA-DQA1 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs2187668 6.00E-28 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2187668 7.27E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_002122 HLA-DQA1 21131588 http://www.ncbi.nlm.nih.gov/pubmed/21131588 "Leukemia, Lymphoid" rs9272535 9.00E-08 Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL. NHGRI|-1
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs17612633 6.97E-13 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs17843604 2.52E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs17612858 1.24E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002122 HLA-DQA1 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs9273349 7.00E-14 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9273349 8.31E-13 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002122 HLA-DQA1 18758464 http://www.ncbi.nlm.nih.gov/pubmed/18758464 Inflammatory Bowel Diseases rs477515 1.00E-08 Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. NHGRI|-1
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9270856 3.56E-17 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2858870 6.07E-83 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9270984 2.73E-15 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002122 HLA-DQA1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9270986 3.46E-39 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002122 HLA-DQA1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Arthritis, Rheumatoid" rs615672 8.00E-27 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9271055 2.22E-15 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9271100 4.92E-17 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002122 HLA-DQA1 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs9271100 1.00E-12 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_002122 HLA-DQA1 17804836 http://www.ncbi.nlm.nih.gov/pubmed/17804836 "Arthritis, Rheumatoid" rs660895 1.00E-108 TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. NHGRI|-1
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9271170 4.92E-17 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002122 HLA-DQA1 21131588 http://www.ncbi.nlm.nih.gov/pubmed/21131588 "Leukemia, Lymphoid" rs674313 7.00E-09 Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL. NHGRI|-1
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs642093 1.10E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9271348 1.71E-15 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002122 HLA-DQA1 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs9271366 3.00E-33 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_002122 HLA-DQA1 21699788 http://www.ncbi.nlm.nih.gov/pubmed/21699788 Inflammatory Bowel Diseases rs9271366 2.00E-70 HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease. NHGRI|-1
NM_002122 HLA-DQA1 21699788 http://www.ncbi.nlm.nih.gov/pubmed/21699788 Inflammatory Bowel Diseases rs9271366 3.00E-31 HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease. NHGRI|-1
NM_002122 HLA-DQA1 21699788 http://www.ncbi.nlm.nih.gov/pubmed/21699788 Inflammatory Bowel Diseases rs9271366 8.00E-11 HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease. NHGRI|-1
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9271366 1.46E-17 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002122 HLA-DQA1 20598377 http://www.ncbi.nlm.nih.gov/pubmed/20598377 Multiple Sclerosis rs9271366 4.00E-17 Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. NHGRI|-1
NM_002122 HLA-DQA1 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs9271366 7.00E-184 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_002122 HLA-DQA1 20512145 http://www.ncbi.nlm.nih.gov/pubmed/20512145 Nasopharyngeal Neoplasms rs28421666 2.00E-18 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. NHGRI|-1
NM_002122 HLA-DQA1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3129768 4.83E-35 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002122 HLA-DQA1 21653640 http://www.ncbi.nlm.nih.gov/pubmed/21653640 "Arthritis, Rheumatoid" rs9272219 1.00E-45 Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways. NHGRI|-1
NM_002122 HLA-DQA1 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs9272219 7.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_002122 HLA-DQA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs3104369 9.94E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002122 HLA-DQA1 20453840 http://www.ncbi.nlm.nih.gov/pubmed/20453840 Multiple Sclerosis rs2040406 1.00E-20 Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis. NHGRI|-1
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1063355 1.33E-219 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs1063355 8.09E-13 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs1049225 3.04E-11 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 21570397 http://www.ncbi.nlm.nih.gov/pubmed/21570397 Drug-Induced Liver Injury rs9274407 5.00E-14 Susceptibility to Amoxicillin-Clavulanate-Induced Liver Injury Is Influenced by Multiple HLA Class I and II Alleles. NHGRI|-1
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9274407 6.72E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9274689 6.50E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9274741 4.72E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9274759 7.24E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs28891406 1.62E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs17212090 7.46E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9275141 2.61E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs9275141 7.42E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2856695 7.66E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs17212420 1.11E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4538747 6.53E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs7774434 3.00E-26 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_002123 HLA-DQB1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs7774434 4.00E-34 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_002123 HLA-DQB1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs9469220 2.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9469220 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_002123 HLA-DQB1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9469220 4.45E-18 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2157051 1.32E-252 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9275224 2.32E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9275224 4.45E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9275245 2.28E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs5000634 7.40E-12 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs3129720 4.91E-11 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 18668548 http://www.ncbi.nlm.nih.gov/pubmed/18668548 "Arthritis, Rheumatoid" rs6457617 1.00E-09 Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility. NHGRI|-1
NM_002123 HLA-DQB1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Arthritis, Rheumatoid" rs6457617 5.00E-75 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs6457617 1.31E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs6457617 3.61E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6457617 9.47E-15 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002123 HLA-DQB1 20383147 http://www.ncbi.nlm.nih.gov/pubmed/20383147 "Scleroderma, Systemic" rs6457617 4.00E-17 Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. NHGRI|-1
NM_002123 HLA-DQB1 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs6457617 2.00E-37 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_002123 HLA-DQB1 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 "Arthritis, Rheumatoid" rs6457620 4.00E-186 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_002123 HLA-DQB1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6457620 3.41E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2647012 3.97E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2647012 1.27E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2647012 2.19E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_002123 HLA-DQB1 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs2647012 8.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_002123 HLA-DQB1 21533074 http://www.ncbi.nlm.nih.gov/pubmed/21533074 "Lymphoma, Follicular" rs2647012 2.00E-21 GWAS of follicular lymphoma reveals allelic heterogeneity at 6p21.32 and suggests shared genetic susceptibility with diffuse large B-cell lymphoma. NHGRI|-1
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9357152 1.91E-141 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9357152 1.80E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9357152 8.42E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 20639881 http://www.ncbi.nlm.nih.gov/pubmed/20639881 "Lymphoma, Follicular" rs10484561 1.00E-29 Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. NHGRI|-1
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1794282 2.48E-103 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1794282 2.21E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1794282 4.01E-18 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2856726 5.09E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2856725 2.05E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2856725 1.11E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 "Diabetes Mellitus, Type 1" rs2647044 1.00E-16 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NM_002123 HLA-DQB1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2647046 1.04E-20 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2647050 5.38E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2856718 5.33E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2856717 1.70E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2856717 1.03E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2858305 1.70E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2858305 7.88E-14 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 20453841 http://www.ncbi.nlm.nih.gov/pubmed/20453841 "Arthritis, Rheumatoid" rs13192471 2.00E-58 A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. NHGRI|-1
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs16898264 3.85E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs9275572 1.00E-35 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_002123 HLA-DQB1 21499248 http://www.ncbi.nlm.nih.gov/pubmed/21499248 "Carcinoma, Hepatocellular" rs9275572 6.00E-09 Genome-wide association study identifies a susceptibility locus for HCV-induced hepatocellular carcinoma. NHGRI|-1
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs9275572 1.37E-09 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9275572 6.41E-14 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9275572 1.74E-20 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs12203586 5.74E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002123 HLA-DQB1 21452313 http://www.ncbi.nlm.nih.gov/pubmed/21452313 "Arthritis, Rheumatoid" rs7765379 5.00E-23 Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci. NHGRI|-1
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs7745656 3.18E-161 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2647087 1.87E-16 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2858333 8.55E-16 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2858331 3.49E-160 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2858331 1.99E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 "Glomerulonephritis, IGA" rs9275596 2.00E-26 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9275596 1.21E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9275596 3.33E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs9275596 6.60E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs3104405 3.47E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs12177980 5.87E-92 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9275659 1.93E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9275686 2.51E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_002123 HLA-DQB1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9275765 3.30E-21 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002123 HLA-DQB1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9275772 7.53E-22 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9461799 4.85E-92 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002123 HLA-DQB1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9461799 1.59E-08 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002123 HLA-DQB1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9469240 7.88E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002123 HLA-DQB1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9275793 3.13E-21 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002123 HLA-DQB1 20711174 http://www.ncbi.nlm.nih.gov/pubmed/20711174 Narcolepsy rs2858884 3.00E-08 Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy. NHGRI|-1
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs13199787 2.51E-96 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs17612633 6.97E-13 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs17843604 2.52E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs17612858 1.24E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002123 HLA-DQB1 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs9273349 7.00E-14 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_002123 HLA-DQB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9273349 8.31E-13 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002124 HLA-DRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9270467 7.00E-17 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002124 HLA-DRB1 18758464 http://www.ncbi.nlm.nih.gov/pubmed/18758464 Inflammatory Bowel Diseases rs477515 1.00E-08 Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. NHGRI|-1
NM_002124 HLA-DRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9270856 3.56E-17 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002124 HLA-DRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2858870 6.07E-83 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002124 HLA-DRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9270984 2.73E-15 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002124 HLA-DRB1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9270986 3.46E-39 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002124 HLA-DRB1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Arthritis, Rheumatoid" rs615672 8.00E-27 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_002124 HLA-DRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9271055 2.22E-15 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002124 HLA-DRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9271100 4.92E-17 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002124 HLA-DRB1 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs9271100 1.00E-12 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_002124 HLA-DRB1 17804836 http://www.ncbi.nlm.nih.gov/pubmed/17804836 "Arthritis, Rheumatoid" rs660895 1.00E-108 TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. NHGRI|-1
NM_002124 HLA-DRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9271170 4.92E-17 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002124 HLA-DRB1 21131588 http://www.ncbi.nlm.nih.gov/pubmed/21131588 "Leukemia, Lymphoid" rs674313 7.00E-09 Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL. NHGRI|-1
NM_002124 HLA-DRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs642093 1.10E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002124 HLA-DRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9271348 1.71E-15 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002124 HLA-DRB1 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs9271366 3.00E-33 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_002124 HLA-DRB1 21699788 http://www.ncbi.nlm.nih.gov/pubmed/21699788 Inflammatory Bowel Diseases rs9271366 2.00E-70 HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease. NHGRI|-1
NM_002124 HLA-DRB1 21699788 http://www.ncbi.nlm.nih.gov/pubmed/21699788 Inflammatory Bowel Diseases rs9271366 3.00E-31 HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease. NHGRI|-1
NM_002124 HLA-DRB1 21699788 http://www.ncbi.nlm.nih.gov/pubmed/21699788 Inflammatory Bowel Diseases rs9271366 8.00E-11 HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease. NHGRI|-1
NM_002124 HLA-DRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9271366 1.46E-17 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002124 HLA-DRB1 20598377 http://www.ncbi.nlm.nih.gov/pubmed/20598377 Multiple Sclerosis rs9271366 4.00E-17 Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. NHGRI|-1
NM_002124 HLA-DRB1 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs9271366 7.00E-184 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_002124 HLA-DRB1 20512145 http://www.ncbi.nlm.nih.gov/pubmed/20512145 Nasopharyngeal Neoplasms rs28421666 2.00E-18 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. NHGRI|-1
NM_002124 HLA-DRB1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3129768 4.83E-35 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002124 HLA-DRB1 21653640 http://www.ncbi.nlm.nih.gov/pubmed/21653640 "Arthritis, Rheumatoid" rs9272219 1.00E-45 Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways. NHGRI|-1
NM_002124 HLA-DRB1 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs9272219 7.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_002124 HLA-DRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs3104369 9.94E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002124 HLA-DRB1 20453840 http://www.ncbi.nlm.nih.gov/pubmed/20453840 Multiple Sclerosis rs2040406 1.00E-20 Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis. NHGRI|-1
NM_002124 HLA-DRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9269329 1.94E-16 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002125 HLA-DRB5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs28490179 1.42E-13 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_002125 HLA-DRB5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs6903608 1.55E-144 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002125 HLA-DRB5 21037568 http://www.ncbi.nlm.nih.gov/pubmed/21037568 Hodgkin Disease rs6903608 3.00E-50 "A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)." NHGRI|-1
NM_002125 HLA-DRB5 21653640 http://www.ncbi.nlm.nih.gov/pubmed/21653640 "Arthritis, Rheumatoid" rs9268853 5.00E-109 Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways. NHGRI|-1
NM_002125 HLA-DRB5 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs9268853 1.00E-55 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_002125 HLA-DRB5 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9268853 1.31E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002125 HLA-DRB5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9268853 8.87E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002125 HLA-DRB5 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9268858 2.00E-08 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002125 HLA-DRB5 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs9268877 4.00E-23 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_002125 HLA-DRB5 18836448 http://www.ncbi.nlm.nih.gov/pubmed/18836448 "Colitis, Ulcerative" rs9268877 6.00E-18 "Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility." NHGRI|-1
NM_002125 HLA-DRB5 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9268877 4.75E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002125 HLA-DRB5 21602797 http://www.ncbi.nlm.nih.gov/pubmed/21602797 Cystic Fibrosis rs9268905 1.00E-07 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. NHGRI|-1
NM_002125 HLA-DRB5 20228798 http://www.ncbi.nlm.nih.gov/pubmed/20228798 "Colitis, Ulcerative" rs9268923 4.00E-15 Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). NHGRI|-1
NM_002125 HLA-DRB5 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs2395185 1.00E-16 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_002125 HLA-DRB5 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 "Colitis, Ulcerative" rs2395185 5.00E-22 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_002127 HLA-G 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs77983016 2.67E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002127 HLA-G 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3132726 2.93E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002127 HLA-G 21570397 http://www.ncbi.nlm.nih.gov/pubmed/21570397 Drug-Induced Liver Injury rs2523822 2.00E-10 Susceptibility to Amoxicillin-Clavulanate-Induced Liver Injury Is Influenced by Multiple HLA Class I and II Alleles. NHGRI|-1
NM_002127 HLA-G 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112125423 2.59E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002127 HLA-G 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112619668 2.97E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002127 HLA-G 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3094654 1.17E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002127 HLA-G 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9258966 1.02E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002127 HLA-G 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2743931 3.71E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002127 HLA-G 21653640 http://www.ncbi.nlm.nih.gov/pubmed/21653640 "Arthritis, Rheumatoid" rs1610677 4.00E-15 Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways. NHGRI|-1
NM_002128 HMGB1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs11618202 7.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_002131 HMGA1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1776897 1.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_002131 HMGA1 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs1776897 7.00E-06 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_002131 HMGA1 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs1776897 8.00E-11 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_002144 HOXB1 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs6504340 6.00E-07 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_002145 HOXB2 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs6504340 6.00E-07 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_002163 IRF8 21131588 http://www.ncbi.nlm.nih.gov/pubmed/21131588 "Leukemia, Lymphoid" rs391525 3.00E-09 Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL. NHGRI|-1
NM_002163 IRF8 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs305061 4.00E-07 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_002163 IRF8 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs16940202 6.00E-19 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_002163 IRF8 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs17445836 4.00E-09 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_002163 IRF8 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs11117432 5.00E-11 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_002163 IRF8 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs987052 8.15E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_002163 IRF8 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs2696835 3.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_002163 IRF8 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, HDL" rs11641231 8.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_002166 ID2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2352714 8.20E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_002166 ID2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7591430 5.64E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_002166 ID2 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs13008689 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_002181 IHH 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1052483 1.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_002182 IL1RAP 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs9290936 4.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_002182 IL1RAP 18385676 http://www.ncbi.nlm.nih.gov/pubmed/18385676 Lung Neoplasms rs7626795 8.00E-06 Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. NHGRI|-1
NM_002185 IL7R 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs6897932 8.00E-06 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_002185 IL7R 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs6897932 2.00E-06 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_002185 IL7R 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6897932 3.00E-07 Risk alleles for multiple sclerosis identified by a genomewide study. NHGRI|-1
NM_002185 IL7R 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs3194051 4.00E-08 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_002185 IL7R 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2194225 6.57E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_002187 IL12B 19169255 http://www.ncbi.nlm.nih.gov/pubmed/19169255 Psoriasis rs3213094 3.00E-26 Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21. NHGRI|-1
NM_002187 IL12B 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs3213094 5.00E-11 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_002187 IL12B 20953188 http://www.ncbi.nlm.nih.gov/pubmed/20953188 Psoriasis rs2546890 1.00E-20 Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. NHGRI|-1
NM_002187 IL12B 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs10045431 4.00E-13 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_002187 IL12B 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs10045431 7.00E-08 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_002187 IL12B 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs6556416 2.00E-08 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_002187 IL12B 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs6887695 9.00E-06 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_002187 IL12B 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6871626 1.00E-21 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_002187 IL12B 20953186 http://www.ncbi.nlm.nih.gov/pubmed/20953186 "Arthritis, Psoriatic" rs12188300 7.00E-17 Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. NHGRI|-1
NM_002187 IL12B 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs2082412 2.00E-28 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NM_002188 IL13 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs1295686 1.00E-07 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_002188 IL13 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs20541 5.00E-15 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NM_002192 INHBA 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs29880 7.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_002192 INHBA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11505535 6.37E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_002192 INHBA 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1079866 6.00E-14 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_002192 INHBA 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Height rs10486715 3.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_002193 INHBB 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs7581710 2.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_002193 INHBB 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs934721 1.81E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_002195 INSL4 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 "Colitis, Ulcerative" rs10975003 1.00E-06 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_002198 IRF1 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4705952 1.00E-08 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_002198 IRF1 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Eosinophils rs4143832 1.00E-10 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_002198 IRF1 20031576 http://www.ncbi.nlm.nih.gov/pubmed/20031576 Fibrinogen rs2522056 1.00E-15 Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. NHGRI|-1
NM_002199 IRF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs796988 2.64E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_002207 ITGA9 19478819 http://www.ncbi.nlm.nih.gov/pubmed/19478819 Nasopharyngeal Neoplasms rs189897 7.00E-08 A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma. NHGRI|-1
NM_002208 ITGAE 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs220470 1.00E-07 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_002209 ITGAL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2285459 3.38E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_002211 ITGB1 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs11009175 5.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_002212 EIF6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs619865 5.21E-04 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_002212 EIF6 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Melanosis rs619865 5.00E-14 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_002215 ITIH1 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs1042779 2.00E-07 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_002222 ITPR1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs746039 2.06E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_002223 ITPR2 17827064 http://www.ncbi.nlm.nih.gov/pubmed/17827064 Amyotrophic Lateral Sclerosis rs2306677 3.00E-06 ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study. NHGRI|-1
NM_002223 ITPR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4964010 4.67E-06 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_002223 ITPR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs3782309 1.01E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_002223 ITPR2 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs718314 2.00E-17 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_002224 ITPR3 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs999943 1.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_002228 JUN 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs4601609 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_002232 KCNA3 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs12061304 1.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_002232 KCNA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs343819 7.98E-06 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_002232 KCNA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4631693 7.53E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_002232 KCNA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs718463 5.28E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_002234 KCNA5 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7302032 4.99E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_002234 KCNA5 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs12302829 8.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_002240 KCNJ6 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2836079 8.86E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_002240 KCNJ6 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs2835810 6.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_002245 KCNK1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs10910200 6.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_002247 KCNMA1 21708048 http://www.ncbi.nlm.nih.gov/pubmed/21708048 Obesity rs2116830 3.00E-10 Genome Wide Association Study Identifies KCNMA1 Contributing to Human Obesity. NHGRI|-1
NM_002247 KCNMA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1247755 7.47E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_002247 KCNMA1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2917454 3.30E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_002247 KCNMA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12219105 9.68E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_002247 KCNMA1 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs4979906 7.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_002249 KCNN3 20173747 http://www.ncbi.nlm.nih.gov/pubmed/20173747 Atrial Fibrillation rs13376333 2.00E-21 Common variants in KCNN3 are associated with lone atrial fibrillation. NHGRI|-1
NM_002252 KCNS3 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2345089 5.11E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_002252 KCNS3 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs16984239 2.00E-06 Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_002252 KCNS3 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs16984239 6.04E-06 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_002252 KCNS3 18084291 http://www.ncbi.nlm.nih.gov/pubmed/18084291 Amyotrophic Lateral Sclerosis rs7580332 9.00E-06 Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis. NHGRI|-1
NM_002265 KPNB1 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs8070463 5.00E-08 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_002285 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs13385193 2.82E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_002285 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17437101 6.31E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_002285 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6736239 5.21E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_002285 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17352801 8.79E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_002285 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6743817 2.70E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_002285 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10199628 2.67E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_002285 AFF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17023516 3.31E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_002285 AFF3 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs11676922 1.00E-14 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_002285 AFF3 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs9653442 5.00E-06 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_002285 AFF3 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs10865035 2.00E-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_002291 LAMB1 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs2158836 7.00E-06 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_002299 LCT 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2164210 1.55E-06 NBL-GWAS version 1 dbGaP|2845
NM_002303 LEPR 20167575 http://www.ncbi.nlm.nih.gov/pubmed/20167575 "Receptors, Leptin" rs1751492 6.00E-13 Genome-wide association study identifies polymorphisms in LEPR as determinants of plasma soluble leptin receptor levels. NHGRI|-1
NM_002303 LEPR 19567438 http://www.ncbi.nlm.nih.gov/pubmed/19567438 C-Reactive Protein rs6700896 3.00E-14 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. NHGRI|-1
NM_002309 LIF 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs5753037 3.00E-16 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_002309 LIF 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2412980 4.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_002309 LIF 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs713875 7.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_002311 LIG3 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs2074518 6.00E-12 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_002312 LIG4 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10492664 1.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_002315 LMO1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs110419 3.91E-07 NBL-GWAS version 1 dbGaP|2845
NM_002315 LMO1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs110419 5.12E-10 NBL-GWAS version 2 dbGaP|2895
NM_002315 LMO1 21124317 http://www.ncbi.nlm.nih.gov/pubmed/21124317 Neuroblastoma rs110419 5.00E-16 Integrative genomics identifies LMO1 as a neuroblastoma oncogene. NHGRI|-1
NM_002315 LMO1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs204938 1.15E-05 NBL-GWAS version 2 dbGaP|2895
NM_002315 LMO1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4758051 2.83E-08 NBL-GWAS version 2 dbGaP|2895
NM_002315 LMO1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10840002 6.01E-06 NBL-GWAS version 2 dbGaP|2895
NM_002316 LMX1B 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs867559 1.00E-07 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_002332 LRP1 21666692 http://www.ncbi.nlm.nih.gov/pubmed/21666692 Migraine Disorders rs11172113 4.00E-09 Genome-wide association study reveals three susceptibility loci for common migraine in the general population. NHGRI|-1
NM_002334 LRP4 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs2306029 8.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_002335 LRP5 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs599083 5.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_002335 LRP5 18455228 http://www.ncbi.nlm.nih.gov/pubmed/18455228 Bone Density rs3736228 6.00E-12 "Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study." NHGRI|-1
NM_002339 LSP1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs907611 1.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_002339 LSP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11041553 2.86E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_002339 LSP1 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs3817198 3.00E-09 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_002342 LTBR 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs11616188 4.00E-12 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_002342 LTBR 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs11064153 5.39E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_002343 LTF 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs1015164 9.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_002351 SH2D1A 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1846322 9.49E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_002351 SH2D1A 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1781115 1.67E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_002358 MAD2L1 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs1845344 7.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_002370 MAGOH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17785382 1.74E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_002372 MAN2A1 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Plasminogen Activator Inhibitor 1 rs4460176 3.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_002373 MAP1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2245715 1.44E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_002374 MAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9288410 2.71E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_002374 MAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9288410 3.28E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_002374 MAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9288410 5.64E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_002379 MATN1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1932397 7.14E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_002379 MATN1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9286938 9.14E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_002379 MATN1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs4949526 4.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_002379 MATN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11580589 2.48E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_002379 MATN1 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs910696 3.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_002379 MATN1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs2180233 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_002382 MAX 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4466998 5.00E-08 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_002382 MAX 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Waist Circumference rs7158173 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_002387 MCC 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs1318772 1.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_002393 MDM4 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs12143943 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_002396 ME2 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs732528 7.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_002397 MEF2C 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs770189 3.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_002397 MEF2C 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs10037512 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_002397 MEF2C 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1366594 1.00E-13 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_002397 MEF2C 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs1366594 1.00E-07 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_002397 MEF2C 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs1366594 8.00E-10 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_002397 MEF2C 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs12518099 7.00E-07 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_002397 MEF2C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2972956 6.07E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_002397 MEF2C 21060863 http://www.ncbi.nlm.nih.gov/pubmed/21060863 Retinal Vein rs17421627 7.00E-16 "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo." NHGRI|-1
NM_002398 MEIS1 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs11897119 5.00E-11 Genome-wide association study of PR interval. NHGRI|-1
NM_002398 MEIS1 17637780 http://www.ncbi.nlm.nih.gov/pubmed/17637780 Restless Legs Syndrome rs2300478 3.00E-28 Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. NHGRI|-1
NM_002398 MEIS1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4671709 4.31E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_002399 MEIS2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs8041675 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_002399 MEIS2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs1568679 1.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_002401 MAP3K3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs7209435 7.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_002403 MFAP2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2284746 4.00E-29 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_002406 MGAT1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 "Cholesterol, HDL" rs655601 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_002406 MGAT1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs12517906 6.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_002406 MGAT1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs12517906 7.00E-08 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_002410 MGAT5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs3748900 5.77E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_002410 MGAT5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2118844 2.78E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_002410 MGAT5 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2118844 4.35E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_002410 MGAT5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6711228 6.58E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_002411 SCGB2A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7129637 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_002412 MGMT 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Vitamin K 1 rs2387326 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_002412 MGMT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1314589 3.95E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_002412 MGMT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1314589 8.76E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_002412 MGMT 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs11818629 3.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_002412 MGMT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs541392 6.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_002413 MGST2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs8192013 4.55E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_002417 MKI67 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Vitamin K 1 rs2387326 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_002417 MKI67 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1314589 3.95E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_002417 MKI67 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1314589 8.76E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_002417 MKI67 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs11818629 3.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_002417 MKI67 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs541392 6.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_002418 MLN 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs2274459 6.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_002420 TRPM1 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs17815774 3.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_002422 MMP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs610950 1.61E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_002422 MMP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs613804 3.38E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_002422 MMP3 20031604 http://www.ncbi.nlm.nih.gov/pubmed/20031604 Matrix Metalloproteinases rs11225434 9.00E-29 Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels. NHGRI|-1
NM_002422 MMP3 20031604 http://www.ncbi.nlm.nih.gov/pubmed/20031604 Matrix Metalloproteinases rs495366 6.00E-34 Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels. NHGRI|-1
NM_002430 MN1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs5761945 6.00E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_002430 MN1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs5761945 7.87E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_002430 MN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs926837 1.06E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_002430 MN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs9608617 3.52E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_002430 MN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2207362 4.08E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_002430 MN1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs5752592 3.28E-06 NBL-GWAS version 1 dbGaP|2845
NM_002430 MN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs5752592 5.21E-05 NBL-GWAS version 2 dbGaP|2895
NM_002430 MN1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs5762311 7.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_002433 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3135050 2.42E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002433 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071653 2.34E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002433 MOG 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal Neoplasms rs29232 9.00E-17 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_002433 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3131854 2.54E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002435 MPI 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8025170 1.54E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_002435 MPI 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8029351 1.54E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_002438 MRC1 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Aspartate Aminotransferases rs2477664 1.00E-16 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_002441 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3749953 2.36E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002441 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3131379 7.24E-85 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_002441 MSH5 18204446 http://www.ncbi.nlm.nih.gov/pubmed/18204446 "Lupus Erythematosus, Systemic" rs3131379 2.00E-52 "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci." NHGRI|-1
NM_002441 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3131379 4.89E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_002443 MSMB 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs10993994 7.00E-13 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_002443 MSMB 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs10993994 3.00E-08 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_002443 MSMB 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs10993994 5.00E-06 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_002443 MSMB 18264096 http://www.ncbi.nlm.nih.gov/pubmed/18264096 Prostatic Neoplasms rs10993994 7.00E-13 Multiple loci identified in a genome-wide association study of prostate cancer. NHGRI|-1
NM_002443 MSMB 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs10993994 9.00E-29 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_002444 MSN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7050592 8.86E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_002444 MSN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs5965007 5.41E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_002444 MSN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs5964445 8.86E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_002445 MSR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs8181023 8.82E-05 NBL-GWAS version 2 dbGaP|2895
NM_002448 MSX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6817411 2.98E-06 NBL-GWAS version 2 dbGaP|2895
NM_002448 MSX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7679624 7.00E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_002449 MSX2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs11134893 2.24E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_002451 MTAP 19578364 http://www.ncbi.nlm.nih.gov/pubmed/19578364 Melanoma rs7023329 4.00E-07 Genome-wide association study identifies three loci associated with melanoma risk. NHGRI|-1
NM_002451 MTAP 19578365 http://www.ncbi.nlm.nih.gov/pubmed/19578365 Dysplastic Nevus Syndrome rs4636294 3.00E-15 Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. NHGRI|-1
NM_002454 MTRR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs2388004 6.00E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_002456 MUC1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs4072037 2.00E-36 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_002456 MUC1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs4072037 4.00E-07 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_002457 MUC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12146505 3.68E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_002460 IRF4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs12203592 2.00E-15 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_002460 IRF4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12203592 2.00E-28 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_002460 IRF4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12203592 4.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_002460 IRF4 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs12203592 7.00E-127 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_002460 IRF4 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs12203592 9.00E-28 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_002460 IRF4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Melanosis rs12203592 2.00E-91 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_002460 IRF4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12203592 4.90E-05 NBL-GWAS version 2 dbGaP|2895
NM_002460 IRF4 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs12203592 6.00E-15 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_002460 IRF4 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs872071 2.00E-20 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NM_002460 IRF4 21131588 http://www.ncbi.nlm.nih.gov/pubmed/21131588 "Leukemia, Lymphoid" rs9378805 2.00E-06 Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL. NHGRI|-1
NM_002460 IRF4 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Melanosis rs1540771 4.00E-18 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_002460 IRF4 21700618 http://www.ncbi.nlm.nih.gov/pubmed/21700618 "Carcinoma, Basal Cell" rs12210050 1.00E-09 Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma. NHGRI|-1
NM_002460 IRF4 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs12210050 5.00E-14 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_002460 IRF4 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1033180 6.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_002467 MYC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4404878 1.19E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_002467 MYC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4404878 3.02E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_002467 MYC 17401363 http://www.ncbi.nlm.nih.gov/pubmed/17401363 Prostatic Neoplasms rs1447295 2.00E-14 Genome-wide association study of prostate cancer identifies a second risk locus at 8q24. NHGRI|-1
NM_002467 MYC 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs1447295 2.00E-19 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_002467 MYC 17401366 http://www.ncbi.nlm.nih.gov/pubmed/17401366 Prostatic Neoplasms rs1447295 6.00E-18 Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24. NHGRI|-1
NM_002467 MYC 18264096 http://www.ncbi.nlm.nih.gov/pubmed/18264096 Prostatic Neoplasms rs4242382 3.00E-19 Multiple loci identified in a genome-wide association study of prostate cancer. NHGRI|-1
NM_002467 MYC 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs4242384 2.00E-24 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_002467 MYC 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs4242384 3.00E-16 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_002467 MYC 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs4242384 3.00E-16 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_002467 MYC 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs7837688 1.00E-25 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_002467 MYC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs6470531 1.63E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_002467 MYC 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs9642880 2.00E-18 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_002467 MYC 20348956 http://www.ncbi.nlm.nih.gov/pubmed/20348956 Urinary Bladder Neoplasms rs9642880 7.00E-12 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_002467 MYC 18794855 http://www.ncbi.nlm.nih.gov/pubmed/18794855 Urinary Bladder Neoplasms rs9642880 9.00E-12 Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_002470 MYH3 19465909 http://www.ncbi.nlm.nih.gov/pubmed/19465909 Malaria rs6503319 7.00E-07 Genome-wide and fine-resolution association analysis of malaria in West Africa. NHGRI|-1
NM_002471 MYH6 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Heart Rate rs365990 9.00E-11 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_002471 MYH6 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs452036 4.00E-14 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_002473 MYH9 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs735854 9.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_002484 NUBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4780986 9.42E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_002489 NDUFA4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12667020 3.75E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_002489 NDUFA4 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs17162294 7.86E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_002489 NDUFA4 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 CD40 Ligand rs7778619 3.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_002495 NDUFS4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs271221 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_002495 NDUFS4 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1504212 2.05E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_002504 NFX1 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs12336160 1.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_002506 NGF 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs195204 9.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_002507 NGFR 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs1035050 9.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_002508 NID1 21478494 http://www.ncbi.nlm.nih.gov/pubmed/21478494 Cutaneous nevi rs3768080 7.00E-08 Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk. NHGRI|-1
NM_002514 NOV 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7000665 1.12E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_002514 NOV 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9643136 1.15E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_002514 NOV 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6993464 6.39E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_002514 NOV 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11782176 5.55E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_002514 NOV 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6991756 5.01E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_002515 NOVA1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs1951082 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_002515 NOVA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1956817 6.56E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_002515 NOVA1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs17109831 6.25E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_002526 NT5E 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11752804 1.30E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_002527 NTF3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7302032 4.99E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_002528 NTHL1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs2516739 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_002530 NTRK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs894290 3.03E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_002531 NTSR1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6011913 6.11E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_002531 NTSR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs856937 2.09E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_002531 NTSR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2249938 1.52E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_002533 NVL 21042317 http://www.ncbi.nlm.nih.gov/pubmed/21042317 "Depressive Disorder, Major" rs11579964 4.00E-06 "Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned." NHGRI|-1
NM_002545 OPCML 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7125438 2.08E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_002545 OPCML 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs4397868 3.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_002546 TNFRSF11B 20548944 http://www.ncbi.nlm.nih.gov/pubmed/20548944 Osteoporosis rs2062375 3.00E-11 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. NHGRI|-1
NM_002546 TNFRSF11B 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2062377 4.00E-16 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_002546 TNFRSF11B 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs11995824 7.00E-09 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_002546 TNFRSF11B 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs6469804 7.00E-15 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_002546 TNFRSF11B 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs6993813 3.00E-11 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_002546 TNFRSF11B 18455228 http://www.ncbi.nlm.nih.gov/pubmed/18455228 Bone Density rs4355801 8.00E-10 "Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study." NHGRI|-1
NM_002555 SLC22A18 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs16928809 1.00E-07 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_002563 P2RY1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs6785504 7.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_002563 P2RY1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs9883654 2.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_002564 P2RY2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1783596 1.78E-06 NBL-GWAS version 1 dbGaP|2845
NM_002570 PCSK6 21051773 http://www.ncbi.nlm.nih.gov/pubmed/21051773 Functional Laterality rs11855415 2.00E-08 PCSK6 is associated with handedness in individuals with dyslexia. NHGRI|-1
NM_002572 PAFAH1B2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 "Receptors, Transferrin" rs7112513 6.00E-09 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_002572 PAFAH1B2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs12269901 2.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_002576 PAK1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1377470 9.03E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_002577 PAK2 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs2084385 5.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_002580 REG3A 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs13409348 3.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_002580 REG3A 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs399885 5.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_002580 REG3A 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs7570469 6.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_002581 PAPPA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs2418444 9.39E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_002581 PAPPA 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs7869550 1.00E-06 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_002582 PARN 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1659127 4.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_002583 PAWR 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs7297018 4.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_002584 PAX7 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs12063142 5.00E-07 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_002585 PBX1 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs6670655 3.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_002586 PBX2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs204993 1.45E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_002586 PBX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs176095 2.18E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_002594 PCSK2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs4814615 5.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_002594 PCSK2 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Fibrinogen rs6044777 8.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_002594 PCSK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs6044777 2.96E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_002594 PCSK2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs852069 3.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_002595 CDK17 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs11108495 4.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_002595 CDK17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7312607 9.34E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_002597 PDC 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs10911902 2.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_002599 PDE2A 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs12418204 5.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_002599 PDE2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs341076 4.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_002599 PDE2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs193170 3.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_002600 PDE4B 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 "Atrial Function, Left" rs10493389 7.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_002600 PDE4B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs11208807 3.63E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_002600 PDE4B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2069278 2.18E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_002600 PDE4B 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs1892534 7.00E-21 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_002600 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs1892534 4.77E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_002600 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs2889195 5.95E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_002600 PDE4B 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4420065 4.00E-62 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_002600 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs4420065 6.67E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_002600 PDE4B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs12753193 3.76E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_002600 PDE4B 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Inflammation rs12753193 4.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_002608 PDGFB 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs2413583 1.00E-26 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_002608 PDGFB 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs968451 1.00E-09 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_002608 PDGFB 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs54211 8.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_002614 PDZK1 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs1967017 4.00E-08 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_002614 PDZK1 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs12129861 3.00E-09 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_002627 PFKP 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs729397 8.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_002627 PFKP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2388097 1.09E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_002633 PGM1 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2269241 4.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_002633 PGM1 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs2749097 2.00E-09 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_002633 PGM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11208285 9.59E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_002633 PGM1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2819130 1.23E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_002634 PHB 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs1035050 9.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_002643 PIGF 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs17818399 3.00E-07 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_002646 PIK3C2B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4951373 6.42E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_002647 PIK3C3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs52911 4.93E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_002647 PIK3C3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs649610 4.93E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_002647 PIK3C3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs593248 6.63E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_002647 PIK3C3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs647512 6.63E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_002647 PIK3C3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs620052 3.60E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_002647 PIK3C3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs587686 3.58E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_002647 PIK3C3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs627636 5.49E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_002647 PIK3C3 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs8085804 8.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_002648 PIM1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs262929 1.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_002649 PIK3CG 19221038 http://www.ncbi.nlm.nih.gov/pubmed/19221038 Platelet Count rs342293 1.00E-24 "A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function." NHGRI|-1
NM_002649 PIK3CG 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs342293 2.00E-33 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_002649 PIK3CG 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs17153527 4.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_002653 PITX1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs31198 8.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_002653 PITX1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs254560 1.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_002653 PITX1 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs477687 6.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_002655 PLAG1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10958476 7.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_002655 PLAG1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs7833986 8.00E-10 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_002655 PLAG1 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Body Height rs13273123 1.00E-09 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_002655 PLAG1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs13273123 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_002662 PLD1 21701570 http://www.ncbi.nlm.nih.gov/pubmed/21701570 Body Mass Index rs6794092 2.00E-06 Genome-Wide Association of BMI in African Americans. NHGRI|-1
NM_002664 PLEK 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs17035378 8.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_002664 PLEK 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Sphingomyelins rs9309413 2.00E-09 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_002670 PLS1 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs3773506 9.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_002674 PMCH 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs1520223 9.00E-07 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_002675 PML 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs5742915 5.00E-07 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_002675 PML 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs5742915 2.00E-14 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_002693 POLG 18193045 http://www.ncbi.nlm.nih.gov/pubmed/18193045 Body Height rs4932217 8.00E-07 Common variants in the GDF5-UQCC region are associated with variation in human height. NHGRI|-1
NM_002697 POU2F1 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs9803659 4.00E-06 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_002699 POU3F1 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs12131057 4.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_002701 POU5F1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9501063 2.29E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002701 POU5F1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9263800 6.55E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002701 POU5F1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3130931 1.14E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002701 POU5F1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9263804 1.34E-08 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002701 POU5F1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113112186 2.97E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002701 POU5F1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130501 3.87E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002701 POU5F1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3132524 8.72E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002711 PPP1R3A 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 acylcarnitine rs10953730 2.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_002714 PPP1R10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7759666 3.61E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002714 PPP1R10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9262122 4.72E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_002718 PPP2R3A 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs823968 6.68E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_002719 PPP2R5C 20663923 http://www.ncbi.nlm.nih.gov/pubmed/20663923 Autistic Disorder rs7142002 3.00E-06 A genome-wide scan for common alleles affecting risk for autism. NHGRI|-1
NM_002725 PRELP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6428009 6.92E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_002729 HHEX 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs1111875 3.00E-06 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_002729 HHEX 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1111875 6.00E-10 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_002729 HHEX 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs1111875 6.00E-10 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_002729 HHEX 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs1111875 7.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_002729 HHEX 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs5015480 1.00E-15 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_002729 HHEX 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs5015480 5.00E-06 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_002729 HHEX 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs5015480 7.00E-08 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_002729 HHEX 20862305 http://www.ncbi.nlm.nih.gov/pubmed/20862305 "Diabetes Mellitus, Type 2" rs5015480 9.00E-06 Identification of new genetic risk variants for type 2 diabetes. NHGRI|-1
NM_002729 HHEX 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs2497306 5.00E-09 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_002731 PRKACB 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs1085093 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_002736 PRKAR2B 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs13224682 6.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_002737 PRKCA 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9912468 1.00E-08 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_002737 PRKCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17634425 1.45E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_002737 PRKCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs973753 4.73E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_002737 PRKCA 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7207345 7.48E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_002742 PRKD1 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs11847697 6.00E-11 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_002744 PRKCZ 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs3753242 1.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_002755 MAP2K1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8684 5.35E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002757 MAP2K5 17637780 http://www.ncbi.nlm.nih.gov/pubmed/17637780 Restless Legs Syndrome rs12593813 1.00E-15 Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. NHGRI|-1
NM_002757 MAP2K5 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2241423 1.00E-18 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_002758 MAP2K6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs558076 2.53E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_002758 MAP2K6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs817097 6.22E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_002761 PRM1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs12928822 3.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_002763 PROX1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1795030 9.30E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_002763 PROX1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs17706439 3.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_002763 PROX1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs340874 7.00E-12 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_002763 PROX1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs340874 5.00E-06 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_002767 PRPSAP2 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs4924935 8.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_002771 PRSS3 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs216345 4.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_002772 TMPRSS15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9975541 8.70E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_002775 HTRA1 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs3793917 4.00E-60 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_002775 HTRA1 17053108 http://www.ncbi.nlm.nih.gov/pubmed/17053108 Macular Degeneration rs11200638 8.00E-12 HTRA1 promoter polymorphism in wet age-related macular degeneration. NHGRI|-1
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2248799 1.89E-28 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2248799 2.92E-32 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4752699 8.45E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4752700 1.40E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4752700 2.70E-10 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2284666 1.47E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2300431 1.14E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2300431 1.74E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs763720 2.29E-11 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs763720 3.53E-12 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7902878 9.49E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2014307 1.48E-23 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2014307 4.35E-08 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2014307 4.49E-21 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002775 HTRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2014307 5.43E-07 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_002790 PSMA5 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs1933182 1.00E-07 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_002791 PSMA6 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs8016947 2.00E-11 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_002794 PSMB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6688464 6.00E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_002802 PSMC1 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs8017423 7.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_002809 PSMD3 20172861 http://www.ncbi.nlm.nih.gov/pubmed/20172861 Leukocyte Count rs4794822 6.00E-10 Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count. NHGRI|-1
NM_002809 PSMD3 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs4794822 4.00E-16 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_002820 PTHLH 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs522958 1.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_002820 PTHLH 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs522958 8.00E-07 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_002820 PTHLH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7137085 3.38E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_002828 PTPN2 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs1893217 5.00E-12 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_002828 PTPN2 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1893217 3.00E-10 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_002828 PTPN2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs1893217 4.00E-15 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_002828 PTPN2 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs2847281 2.00E-08 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_002828 PTPN2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs2542151 2.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_002828 PTPN2 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs2542151 3.00E-08 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_002828 PTPN2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2542151 5.00E-17 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_002828 PTPN2 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs2542151 1.00E-14 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_002828 PTPN2 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs2542151 9.00E-08 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_002829 PTPN3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4978813 7.01E-06 NBL-GWAS version 1 dbGaP|2845
NM_002833 PTPN9 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs4886707 8.00E-08 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_002834 PTPN11 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs11066301 8.00E-12 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_002834 PTPN11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs11614063 9.92E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_002834 PTPN11 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs3803064 7.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_002838 PTPRC 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs12127588 7.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_002839 PTPRD 18660810 http://www.ncbi.nlm.nih.gov/pubmed/18660810 Restless Legs Syndrome rs1975197 6.00E-09 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. NHGRI|-1
NM_002839 PTPRD 20174558 http://www.ncbi.nlm.nih.gov/pubmed/20174558 "Diabetes Mellitus, Type 2" rs17584499 9.00E-10 A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. NHGRI|-1
NM_002839 PTPRD 18660810 http://www.ncbi.nlm.nih.gov/pubmed/18660810 Restless Legs Syndrome rs4626664 6.00E-10 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. NHGRI|-1
NM_002839 PTPRD 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs2475335 9.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_002839 PTPRD 21647700 http://www.ncbi.nlm.nih.gov/pubmed/21647700 "Diabetes Mellitus, Type 2" rs649891 6.00E-06 "Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals." NHGRI|-1
NM_002839 PTPRD 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Braces rs1535480 4.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_002839 PTPRD 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7044355 1.00E-07 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_002839 PTPRD 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10815798 6.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_002840 PTPRF 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12069733 8.59E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_002841 PTPRG 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs652889 8.00E-07 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_002841 PTPRG 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs739984 7.19E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_002841 PTPRG 20825314 http://www.ncbi.nlm.nih.gov/pubmed/20825314 Fuchs Endothelial Dystrophy rs10490775 1.00E-06 E2-2 protein and Fuchs's corneal dystrophy. NHGRI|-1
NM_002841 PTPRG 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs10514718 4.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_002843 PTPRJ 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs11039571 9.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_002844 PTPRK 20068591 http://www.ncbi.nlm.nih.gov/pubmed/20068591 Hearing Loss rs10499138 2.00E-06 A genome-wide association study for age-related hearing impairment in the Saami. NHGRI|-1
NM_002844 PTPRK 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs802734 3.00E-14 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_002845 PTPRM 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs7243299 8.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_002845 PTPRM 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs8098064 4.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_002845 PTPRM 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs12455846 5.15E-06 NBL-GWAS version 1 dbGaP|2845
NM_002845 PTPRM 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs16951664 6.29E-06 NBL-GWAS version 1 dbGaP|2845
NM_002847 PTPRN2 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs6459804 8.00E-06 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_002847 PTPRN2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs10227331 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_002849 PTPRR 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2470378 6.28E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_002850 PTPRS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4807016 8.29E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_002851 PTPRZ1 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs10253361 6.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_002856 PVRL2 20885792 http://www.ncbi.nlm.nih.gov/pubmed/20885792 Alzheimer Disease rs6859 1.00E-07 Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. NHGRI|-1
NM_002856 PVRL2 18823527 http://www.ncbi.nlm.nih.gov/pubmed/18823527 Alzheimer Disease rs6859 6.00E-14 A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. NHGRI|-1
NM_002864 PZP 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs6487679 1.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_002872 RAC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2284037 1.14E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_002872 RAC2 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs13053175 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_002874 RAD23B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs817858 7.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_002874 RAD23B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs17724552 3.92E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_002877 RAD51L1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs911263 2.00E-11 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_002877 RAD51L1 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs1956529 3.00E-08 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_002877 RAD51L1 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs999737 2.00E-07 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_002880 RAF1 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs3729931 7.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_002881 RALB 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs934721 1.81E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_002884 RAP1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10857899 3.06E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_002884 RAP1A 20548944 http://www.ncbi.nlm.nih.gov/pubmed/20548944 Bone Density rs494453 4.00E-08 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. NHGRI|-1
NM_002886 RAP2B 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs6785504 7.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_002886 RAP2B 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs9883654 2.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_002889 RARRES2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4721 5.03E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_002890 RASA1 21173776 http://www.ncbi.nlm.nih.gov/pubmed/21173776 Personality rs2032794 2.00E-06 Meta-analysis of genome-wide association studies for personality. NHGRI|-1
NM_002891 RASGRF1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs3743195 4.06E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_002891 RASGRF1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs3743200 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_002891 RASGRF1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs3816282 2.16E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_002891 RASGRF1 20835236 http://www.ncbi.nlm.nih.gov/pubmed/20835236 Myopia rs939658 2.00E-09 A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. NHGRI|-1
NM_002894 RBBP8 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs4331426 7.00E-09 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_002894 RBBP8 20364137 http://www.ncbi.nlm.nih.gov/pubmed/20364137 Intracranial Aneurysm rs11661542 1.00E-12 Genome-wide association study of intracranial aneurysm identifies three new risk loci. NHGRI|-1
NM_002897 RBMS1 20418489 http://www.ncbi.nlm.nih.gov/pubmed/20418489 "Diabetes Mellitus, Type 2" rs7593730 4.00E-08 Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. NHGRI|-1
NM_002897 RBMS1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs10192369 9.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_002897 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6432628 9.13E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_002897 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13034284 1.85E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_002897 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9967749 8.13E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_002897 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11681327 4.77E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_002897 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7603576 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_002897 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2551691 9.03E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_002897 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs197275 4.42E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_002898 RBMS2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2657888 7.75E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_002901 RCN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs11031676 5.68E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_002901 RCN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7944342 6.98E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_002904 RDBP 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2072633 1.47E-10 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_002904 RDBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4151672 1.74E-09 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002904 RDBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4151672 6.10E-10 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_002904 RDBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs438999 4.89E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_002904 RDBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs438999 5.68E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_002908 REL 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs13031237 8.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_002908 REL 19503088 http://www.ncbi.nlm.nih.gov/pubmed/19503088 "Arthritis, Rheumatoid" rs13017599 2.00E-12 "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis." NHGRI|-1
NM_002908 REL 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs702873 4.00E-09 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_002908 REL 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs842636 6.00E-06 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_002912 REV3L 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs240993 5.00E-20 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_002915 RFC3 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs690705 6.00E-07 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_002916 RFC4 20011104 http://www.ncbi.nlm.nih.gov/pubmed/20011104 Adiponectin rs266717 9.00E-19 A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. NHGRI|-1
NM_002916 RFC4 20011104 http://www.ncbi.nlm.nih.gov/pubmed/20011104 Adiponectin rs1648707 3.00E-12 A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. NHGRI|-1
NM_002916 RFC4 20876611 http://www.ncbi.nlm.nih.gov/pubmed/20876611 Adiponectin rs864265 1.00E-19 Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ. NHGRI|-1
NM_002920 RFX4 21084426 http://www.ncbi.nlm.nih.gov/pubmed/21084426 Parkinson Disease rs4964469 2.00E-07 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. NHGRI|-1
NM_002920 RFX4 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs3891355 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_002922 RGS1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs2816316 2.00E-17 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_002922 RGS1 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs2816316 3.00E-11 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_002923 RGS2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs842796 7.60E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_002923 RGS2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs842796 8.50E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_002924 RGS7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7531849 3.04E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_002925 RGS10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10886492 7.15E-05 NBL-GWAS version 2 dbGaP|2895
NM_002925 RGS10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2991769 3.09E-05 NBL-GWAS version 2 dbGaP|2895
NM_002925 RGS10 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2991769 7.72E-07 NBL-GWAS version 1 dbGaP|2845
NM_002925 RGS10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2991770 1.76E-05 NBL-GWAS version 2 dbGaP|2895
NM_002925 RGS10 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2991770 8.71E-07 NBL-GWAS version 1 dbGaP|2845
NM_002930 RIT2 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs4130047 2.00E-07 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_002930 RIT2 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs17664267 7.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_002930 RIT2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs627636 5.49E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_002930 RIT2 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs8085804 8.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_002942 ROBO2 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs9836484 4.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_002942 ROBO2 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs9831754 8.00E-06 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_002942 ROBO2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Glycoproteins rs9834373 4.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_002943 RORA 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs3743266 8.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_002943 RORA 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs340029 4.00E-09 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_002943 RORA 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs3784609 3.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_002943 RORA 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs11071559 1.00E-07 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_002943 RORA 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs12912233 6.00E-07 Genome-wide association scan of trait depression. NHGRI|-1
NM_002943 RORA 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs809736 8.00E-06 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_002950 RPN1 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs4328821 3.00E-17 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_002950 RPN1 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs4328821 5.00E-40 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_002951 RPN2 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs6031882 6.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_002957 RXRA 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs11185668 2.87E-06 NBL-GWAS version 1 dbGaP|2845
NM_002963 S100A7 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs4845552 6.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_002968 SALL1 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs10521222 9.00E-13 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_002971 SATB1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs6792314 8.60E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_002971 SATB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11914608 1.42E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_002971 SATB1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs13073817 7.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_002971 SATB1 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs6809854 1.00E-07 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_002973 ATXN2 21060863 http://www.ncbi.nlm.nih.gov/pubmed/21060863 Retinal Vein rs10774625 2.00E-13 "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo." NHGRI|-1
NM_002973 ATXN2 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs653178 3.00E-19 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_002973 ATXN2 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs653178 3.00E-18 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_002973 ATXN2 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs653178 7.00E-21 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_002973 ATXN2 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs653178 8.00E-08 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_002973 ATXN2 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Cystatin C rs653178 4.00E-11 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_002973 ATXN2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs11065987 1.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_002973 ATXN2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs11065987 1.00E-12 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_002976 SCN7A 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs13015447 7.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_002982 CCL2 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs3091315 2.00E-13 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_002989 CCL21 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 "Arthritis, Rheumatoid" rs2812378 3.00E-08 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_002990 CCL22 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs8044834 8.68E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_002999 SDC4 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs1008953 1.00E-07 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_002999 SDC4 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs6073708 1.50E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_003003 SEC14L1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs3744064 7.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_003005 SELP 20167578 http://www.ncbi.nlm.nih.gov/pubmed/20167578 P-Selectin rs6136 4.00E-61 Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. NHGRI|-1
NM_003005 SELP 20167578 http://www.ncbi.nlm.nih.gov/pubmed/20167578 P-Selectin rs2235302 4.00E-16 Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. NHGRI|-1
NM_003005 SELP 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs1569476 3.00E-07 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_003006 SELPLG 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs8179116 3.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_003010 MAP2K4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11653406 9.16E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_003010 MAP2K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs8068445 1.10E-05 NBL-GWAS version 2 dbGaP|2895
NM_003011 SET 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4836618 5.41E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_003012 SFRP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4736788 4.88E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_003012 SFRP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10094981 4.82E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_003013 SFRP2 19389651 http://www.ncbi.nlm.nih.gov/pubmed/19389651 Electrocardiography rs17030434 5.00E-06 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. NHGRI|-1
NM_003017 SRSF3 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs1321311 3.00E-10 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_003017 SRSF3 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9470361 3.00E-27 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_003020 SCG5 18372905 http://www.ncbi.nlm.nih.gov/pubmed/18372905 Colorectal Neoplasms rs4779584 5.00E-07 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. NHGRI|-1
NM_003026 SH3GL2 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs10810865 4.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_003026 SH3GL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs1755289 9.84E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_003026 SH3GL2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1755289 3.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_003026 SH3GL2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1755289 9.10E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_003026 SH3GL2 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs2210327 7.00E-07 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_003027 SH3GL3 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs2562784 6.00E-08 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003027 SH3GL3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs2554380 9.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003028 SHB 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs7873102 6.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_003028 SHB 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4878743 1.06E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_003032 ST6GAL1 19483685 http://www.ncbi.nlm.nih.gov/pubmed/19483685 Floxacillin rs10937275 1.00E-08 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. NHGRI|-1
NM_003033 ST3GAL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2978012 8.73E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_003033 ST3GAL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2978015 8.81E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_003033 ST3GAL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2978023 1.81E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_003034 ST8SIA1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs2216228 4.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_003042 SLC6A1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs9990174 6.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_003043 SLC6A6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9834678 5.65E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_003043 SLC6A6 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs9036 3.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_003046 SLC7A2 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs2720508 7.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_003052 SLC34A1 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs6420094 1.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_003057 SLC22A1 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs651164 2.00E-10 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_003057 SLC22A1 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs651164 2.00E-09 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_003058 SLC22A2 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Creatinine rs2279463 6.00E-12 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_003058 SLC22A2 20383145 http://www.ncbi.nlm.nih.gov/pubmed/20383145 Kidney Diseases rs3127573 7.00E-10 Genetic loci influencing kidney function and chronic kidney disease. NHGRI|-1
NM_003058 SLC22A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs410569 2.45E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_003058 SLC22A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs446809 6.51E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_003058 SLC22A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs667538 3.09E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_003058 SLC22A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs415897 2.91E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_003058 SLC22A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs384156 9.10E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_003058 SLC22A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs316169 5.08E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_003058 SLC22A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs316170 2.21E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_003058 SLC22A2 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs651164 2.00E-10 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_003058 SLC22A2 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs651164 2.00E-09 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_003059 SLC22A4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs11950562 3.88E-05 NBL-GWAS version 2 dbGaP|2895
NM_003059 SLC22A4 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs12777 1.00E-06 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_003059 SLC22A4 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs274546 7.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_003060 SLC22A5 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs2073643 2.00E-07 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_003060 SLC22A5 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs6596075 3.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_003060 SLC22A5 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs1016988 1.00E-12 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_003060 SLC22A5 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs274546 7.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_003062 SLIT3 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs4282339 7.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_003062 SLIT3 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs13156607 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_003068 SNAI2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs12155623 3.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_003072 SMARCA4 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11669133 1.00E-08 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_003072 SMARCA4 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs1122608 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_003072 SMARCA4 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs1122608 2.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_003072 SMARCA4 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs11668477 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_003072 SMARCA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs11668477 1.51E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_003079 SMARCE1 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs7221109 1.00E-09 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_003092 SNRPB2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs3787509 9.03E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_003097 SNRPN 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Forced Expiratory Volume rs3867498 1.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_003105 SORL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10892759 4.49E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_003105 SORL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1620003 9.91E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_003105 SORL1 20838585 http://www.ncbi.nlm.nih.gov/pubmed/20838585 Waist Circumference rs7121446 3.00E-06 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. NHGRI|-1
NM_003106 SOX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11926120 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_003106 SOX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs6791663 3.29E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_003107 SOX4 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs9466056 4.00E-06 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_003108 SOX11 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs16864170 2.00E-07 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_003108 SOX11 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs1405262 6.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_003108 SOX11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs13027881 3.76E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003108 SOX11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs6734894 4.63E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003108 SOX11 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs11677370 3.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_003108 SOX11 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1377638 3.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_003108 SOX11 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12692340 8.48E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_003108 SOX11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17363613 8.41E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_003109 SP1 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs10876432 1.00E-07 New sequence variants associated with bone mineral density. NHGRI|-1
NM_003112 SP4 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs17144465 6.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_003112 SP4 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs17144465 8.00E-07 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_003119 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4785684 2.98E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_003119 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3922634 2.73E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_003119 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3922633 2.73E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_003119 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8052076 2.18E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_003119 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4785686 4.74E-06 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_003119 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11862081 5.40E-06 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_003119 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3803680 1.16E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_003119 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3803676 6.47E-06 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_003119 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs463701 6.36E-06 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_003119 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs382745 1.04E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_003119 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2056309 5.13E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_003119 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs457372 8.13E-06 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_003121 SPIB 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs3745516 2.00E-13 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_003121 SPIB 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs3745516 8.00E-11 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_003126 SPTA1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs2779116 3.00E-09 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_003126 SPTA1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs857721 1.00E-10 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_003128 SPTBN1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs11898505 2.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_003128 SPTBN1 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs11898505 4.00E-06 New sequence variants associated with bone mineral density. NHGRI|-1
NM_003128 SPTBN1 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs11898505 8.00E-07 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_003128 SPTBN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6734445 4.13E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_003128 SPTBN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2941579 4.11E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_003134 SRP14 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs7181230 5.00E-11 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_003149 STAC 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs6799705 2.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_003149 STAC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs3996 6.12E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_003150 STAT3 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs744166 7.00E-12 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_003150 STAT3 20159113 http://www.ncbi.nlm.nih.gov/pubmed/20159113 Multiple Sclerosis rs744166 3.00E-10 Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. NHGRI|-1
NM_003151 STAT4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Insulin rs3024896 6.19E-05 Genomewide association analysis of insulin (INS) in a birth cohort from a founder population dbGaP|2901
NM_003151 STAT4 19165918 http://www.ncbi.nlm.nih.gov/pubmed/19165918 "Lupus Erythematosus, Systemic" rs3821236 8.00E-11 Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. NHGRI|-1
NM_003151 STAT4 20383147 http://www.ncbi.nlm.nih.gov/pubmed/20383147 "Scleroderma, Systemic" rs3821236 3.00E-09 Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. NHGRI|-1
NM_003151 STAT4 20453841 http://www.ncbi.nlm.nih.gov/pubmed/20453841 "Arthritis, Rheumatoid" rs7574865 2.00E-06 A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. NHGRI|-1
NM_003151 STAT4 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs7574865 3.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_003151 STAT4 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs7574865 4.00E-10 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_003151 STAT4 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs7574865 2.00E-20 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_003151 STAT4 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs7574865 5.00E-42 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_003151 STAT4 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs7574865 8.96E-14 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_003151 STAT4 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs7574865 8.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_003151 STAT4 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs7574865 9.00E-14 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_003151 STAT4 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs7574865 2.00E-13 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_003151 STAT4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7572482 3.18E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003153 STAT6 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs167769 2.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_003155 STC1 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs10109414 1.00E-08 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_003167 SULT2A1 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs2637125 3.00E-19 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_003174 SVIL 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1927457 8.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_003177 SYK 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic Nephropathies rs773506 6.00E-06 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_003178 SYN2 21314694 http://www.ncbi.nlm.nih.gov/pubmed/21314694 Alcoholism rs6777876 4.00E-07 Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample. NHGRI|-1
NM_003188 MAP3K7 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs713155 5.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_003188 MAP3K7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1145724 4.14E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003188 MAP3K7 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs806276 3.00E-07 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_003192 TBCC 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Bipolar Disorder rs6458307 4.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_003193 TBCE 19557161 http://www.ncbi.nlm.nih.gov/pubmed/19557161 Adiposity rs6429082 3.00E-07 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. NHGRI|-1
NM_003199 TCF4 19571811 http://www.ncbi.nlm.nih.gov/pubmed/19571811 Schizophrenia rs17594526 1.00E-07 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. NHGRI|-1
NM_003199 TCF4 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs9960767 4.00E-09 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_003199 TCF4 20825314 http://www.ncbi.nlm.nih.gov/pubmed/20825314 Fuchs Endothelial Dystrophy rs613872 1.00E-18 E2-2 protein and Fuchs's corneal dystrophy. NHGRI|-1
NM_003199 TCF4 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs1970671 3.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_003204 NFE2L1 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs3764400 4.00E-07 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_003205 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7176873 1.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003205 TCF12 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2733332 4.41E-06 NBL-GWAS version 1 dbGaP|2845
NM_003205 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs16977243 2.74E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003205 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2733333 9.31E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003205 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7175191 1.64E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003206 TCF21 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs12190287 1.00E-12 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_003213 TEAD4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10774085 3.51E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_003215 TEC 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1472971 8.58E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_003221 TFAP2B 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2206277 1.00E-07 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_003221 TFAP2B 19557161 http://www.ncbi.nlm.nih.gov/pubmed/19557161 Adiposity rs987237 2.00E-11 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. NHGRI|-1
NM_003221 TFAP2B 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs987237 3.00E-20 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_003221 TFAP2B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Body Mass Index rs987237 7.37E-07 Genomewide association analysis of body mass index (BMI) in a birth cohort from a founder population dbGaP|2896
NM_003227 TFR2 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Count rs7385804 5.00E-10 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_003227 TFR2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs7385804 4.00E-10 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_003227 TFR2 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs7385804 7.00E-08 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_003227 TFR2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7786877 3.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_003234 TFRC 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9859260 8.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_003234 TFRC 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs11915082 8.00E-13 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_003236 TGFA 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs454305 5.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_003236 TGFA 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs432203 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_003238 TGFB2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1018040 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_003238 TGFB2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1018040 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_003242 TGFBR2 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs3773643 2.00E-07 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_003242 TGFBR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2043136 9.09E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003242 TGFBR2 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs4680878 7.50E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_003242 TGFBR2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9870410 3.76E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_003242 TGFBR2 17903298 http://www.ncbi.nlm.nih.gov/pubmed/17903298 Blood Glucose rs10510634 5.00E-06 Genome-wide association with diabetes-related traits in the Framingham Heart Study. NHGRI|-1
NM_003242 TGFBR2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1117751 1.98E-06 NBL-GWAS version 1 dbGaP|2845
NM_003242 TGFBR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4613502 1.65E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_003243 TGFBR3 19249006 http://www.ncbi.nlm.nih.gov/pubmed/19249006 Bone Density rs17131547 1.00E-06 Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups. NHGRI|-1
NM_003244 TGIF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs431220 5.88E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_003247 THBS2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7741751 2.25E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_003253 TIAM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2268225 5.59E-06 NBL-GWAS version 2 dbGaP|2895
NM_003253 TIAM1 20801718 http://www.ncbi.nlm.nih.gov/pubmed/20801718 Amyotrophic Lateral Sclerosis rs13048019 3.00E-08 Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. NHGRI|-1
NM_003253 TIAM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs1475591 6.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_003256 TIMP4 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs17036101 2.00E-07 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_003256 TIMP4 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs13081389 2.00E-07 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_003257 TJP1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1471225 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_003263 TLR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7696175 1.41E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_003272 GPR137B 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs7520258 5.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_003276 TMPO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs249851 1.20E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_003281 TNNI1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs16848610 1.93E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_003284 TNP1 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs6435957 4.00E-07 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_003284 TNP1 17529974 http://www.ncbi.nlm.nih.gov/pubmed/17529974 Breast Neoplasms rs13387042 1.00E-13 Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer. NHGRI|-1
NM_003284 TNP1 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs13387042 2.00E-10 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_003284 TNP1 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs13387042 2.00E-10 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_003284 TNP1 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs13387042 2.00E-08 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_003284 TNP1 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs13387042 9.00E-06 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_003284 TNP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs13011060 1.50E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_003285 TNR 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs3766680 4.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_003286 TOP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs3092685 1.39E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_003300 TRAF3 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs10133111 5.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_003301 TRHR 19268274 http://www.ncbi.nlm.nih.gov/pubmed/19268274 Adiposity rs7832552 4.00E-10 Genome-wide association and replication studies identified TRHR as an important gene for lean body mass. NHGRI|-1
NM_003306 TRPC4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs17210569 3.59E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_003310 TSSC1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs10199521 3.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_003311 PHLDA2 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs3847646 5.00E-06 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_003316 TTC3 20463881 http://www.ncbi.nlm.nih.gov/pubmed/20463881 Eye Color rs1003719 2.00E-10 Digital quantification of human eye color highlights genetic association of three new loci. NHGRI|-1
NM_003317 NKX2-1 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs17104630 8.00E-06 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003318 TTK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7453746 7.12E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_003318 TTK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7453746 7.86E-06 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_003319 TTN 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs12476289 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_003324 TULP3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10774085 3.51E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_003326 TNFSF4 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs2205960 3.00E-32 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_003326 TNFSF4 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs1342038 4.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_003326 TNFSF4 18204446 http://www.ncbi.nlm.nih.gov/pubmed/18204446 "Lupus Erythematosus, Systemic" rs10798269 1.00E-07 "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci." NHGRI|-1
NM_003331 TYK2 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs12720356 1.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_003331 TYK2 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs12720356 4.00E-11 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_003331 TYK2 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs280519 4.00E-09 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_003331 TYK2 19966805 http://www.ncbi.nlm.nih.gov/pubmed/19966805 "Diabetes Mellitus, Type 2" rs2304256 4.00E-09 The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes. NHGRI|-1
NM_003347 UBE2L3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs181359 5.00E-16 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_003347 UBE2L3 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs5754217 2.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_003347 UBE2L3 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs4821112 1.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_003347 UBE2L3 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs131654 1.00E-16 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_003361 UMOD 20686651 http://www.ncbi.nlm.nih.gov/pubmed/20686651 Waist Circumference rs4293393 4.00E-10 Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases. NHGRI|-1
NM_003361 UMOD 21082022 http://www.ncbi.nlm.nih.gov/pubmed/21082022 Hypertension rs13333226 4.00E-11 Genome-wide association study of blood pressure extremes identifies variant near UMOD associated with hypertension. NHGRI|-1
NM_003361 UMOD 19430482 http://www.ncbi.nlm.nih.gov/pubmed/19430482 Creatinine rs12917707 5.00E-16 Multiple loci associated with indices of renal function and chronic kidney disease. NHGRI|-1
NM_003361 UMOD 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs12917707 1.00E-20 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_003361 UMOD 19430482 http://www.ncbi.nlm.nih.gov/pubmed/19430482 "Kidney Failure, Chronic" rs12917707 2.00E-12 Multiple loci associated with indices of renal function and chronic kidney disease. NHGRI|-1
NM_003361 UMOD 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs12444268 2.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_003371 VAV2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2810545 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_003371 VAV2 20598377 http://www.ncbi.nlm.nih.gov/pubmed/20598377 Multiple Sclerosis rs3780792 1.00E-06 Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. NHGRI|-1
NM_003376 VEGFA 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_003376 VEGFA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_003376 VEGFA 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_003376 VEGFA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_003376 VEGFA 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_003379 EZR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs744893 2.53E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_003381 VIP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs546599 2.19E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_003381 VIP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs633596 5.06E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_003384 VRK1 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4905558 8.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_003384 VRK1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1022590 6.27E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_003384 VRK1 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs1471356 9.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_003384 VRK1 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs17094273 9.00E-08 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_003386 ZAN 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Count rs2075671 1.00E-09 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_003392 WNT5A 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs358806 3.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_003400 XPO1 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs6545883 5.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_003406 YWHAZ 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3491 1.79E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_003406 YWHAZ 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs931812 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_003431 ZNF124 21314694 http://www.ncbi.nlm.nih.gov/pubmed/21314694 Alcoholism rs3738443 4.00E-06 Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample. NHGRI|-1
NM_003443 ZBTB17 21459883 http://www.ncbi.nlm.nih.gov/pubmed/21459883 "Cardiomyopathy, Dilated" rs10927875 1.00E-09 A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. NHGRI|-1
NM_003446 ZNF157 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Optic Nerve rs6611365 4.00E-07 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_003449 TRIM26 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9261547 5.94E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003449 TRIM26 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs4711211 6.60E-07 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_003449 TRIM26 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10947058 2.60E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003449 TRIM26 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2844780 5.50E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_003449 TRIM26 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2844779 1.60E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_003449 TRIM26 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10456378 1.04E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003449 TRIM26 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2844773 1.17E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_003449 TRIM26 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9261588 3.46E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003449 TRIM26 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2844786 1.70E-07 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_003455 ZNF202 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Stomach Neoplasms rs2126709 4.00E-07 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_003455 ZNF202 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9326264 6.90E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003455 ZNF202 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10893085 9.84E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003455 ZNF202 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11219274 8.17E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003458 BSN 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs9858542 7.00E-09 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_003458 BSN 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs9858542 4.00E-08 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_003458 BSN 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs9858542 5.00E-08 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_003465 CHIT1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4950929 1.32E-12 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_003465 CHIT1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs946263 9.74E-13 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_003465 CHIT1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2153101 9.74E-13 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_003467 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4954564 5.21E-06 NBL-GWAS version 1 dbGaP|2845
NM_003467 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1123848 4.90E-06 NBL-GWAS version 1 dbGaP|2845
NM_003467 CXCR4 17903306 http://www.ncbi.nlm.nih.gov/pubmed/17903306 Electrocardiography rs882300 3.00E-07 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. NHGRI|-1
NM_003467 CXCR4 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs882300 1.00E-07 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_003467 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs6430612 4.51E-07 NBL-GWAS version 1 dbGaP|2845
NM_003467 CXCR4 20421499 http://www.ncbi.nlm.nih.gov/pubmed/20421499 Telomere rs4452212 2.00E-06 Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. NHGRI|-1
NM_003467 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs309137 3.48E-07 NBL-GWAS version 1 dbGaP|2845
NM_003467 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs749873 1.79E-06 NBL-GWAS version 1 dbGaP|2845
NM_003467 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2011946 7.16E-06 NBL-GWAS version 1 dbGaP|2845
NM_003467 CXCR4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs932206 1.07E-06 NBL-GWAS version 1 dbGaP|2845
NM_003469 SCG2 20200953 http://www.ncbi.nlm.nih.gov/pubmed/20200953 Osteoporosis rs16864755 4.00E-06 Genome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham Study. NHGRI|-1
NM_003471 KCNAB1 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Aging rs3772255 8.00E-06 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_003476 CSRP3 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs12146588 8.75E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_003483 HMGA2 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs1042725 3.00E-18 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_003483 HMGA2 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs1042725 3.00E-20 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003483 HMGA2 17767157 http://www.ncbi.nlm.nih.gov/pubmed/17767157 Body Height rs1042725 6.00E-16 A common variant of HMGA2 is associated with adult and childhood height in the general population. NHGRI|-1
NM_003483 HMGA2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs8756 2.00E-16 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003483 HMGA2 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs8756 4.00E-07 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_003483 HMGA2 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs8756 5.00E-14 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_003483 HMGA2 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs12424086 4.00E-06 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_003483 HMGA2 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs12424086 8.00E-06 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_003483 HMGA2 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs4026608 2.00E-09 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_003484 HMGA2 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs1042725 3.00E-18 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_003484 HMGA2 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs1042725 3.00E-20 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003484 HMGA2 17767157 http://www.ncbi.nlm.nih.gov/pubmed/17767157 Body Height rs1042725 6.00E-16 A common variant of HMGA2 is associated with adult and childhood height in the general population. NHGRI|-1
NM_003484 HMGA2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs8756 2.00E-16 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003484 HMGA2 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs8756 4.00E-07 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_003484 HMGA2 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs8756 5.00E-14 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_003484 HMGA2 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs12424086 4.00E-06 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_003484 HMGA2 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs12424086 8.00E-06 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_003484 HMGA2 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs4026608 2.00E-09 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_003489 NRIP1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs2229741 6.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_003489 NRIP1 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs1736135 2.00E-07 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_003489 NRIP1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs1736135 7.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_003489 NRIP1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs1297265 7.00E-13 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_003490 SYN3 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs9621532 1.00E-11 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_003490 SYN3 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs9621532 2.00E-15 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_003490 SYN3 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs9621532 4.00E-09 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_003494 DYSF 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Albumins rs2900976 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_003498 SNN 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs8049607 5.00E-15 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_003498 SNN 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs8049607 6.00E-15 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_003502 AXIN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11644916 6.24E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003502 AXIN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11648673 4.77E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003505 FZD1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2974129 9.80E-07 NBL-GWAS version 1 dbGaP|2845
NM_003507 FZD7 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17385675 3.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_003509 HIST1H2AH 19571811 http://www.ncbi.nlm.nih.gov/pubmed/19571811 Schizophrenia rs13194053 1.00E-08 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. NHGRI|-1
NM_003509 HIST1H2AH 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs13194053 1.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_003510 HIST1H2AH 19571811 http://www.ncbi.nlm.nih.gov/pubmed/19571811 Schizophrenia rs13194053 1.00E-08 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. NHGRI|-1
NM_003510 HIST1H2AH 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs13194053 1.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_003511 HIST1H2AH 19571811 http://www.ncbi.nlm.nih.gov/pubmed/19571811 Schizophrenia rs13194053 1.00E-08 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. NHGRI|-1
NM_003511 HIST1H2AH 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs13194053 1.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_003514 HIST1H2AH 19571811 http://www.ncbi.nlm.nih.gov/pubmed/19571811 Schizophrenia rs13194053 1.00E-08 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. NHGRI|-1
NM_003514 HIST1H2AH 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs13194053 1.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_003518 HIST1H2BC 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs12206204 8.00E-07 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_003520 HIST1H2BN 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs175597 8.98E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_003520 HIST1H2BN 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs13194781 2.31E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_003520 HIST1H2BN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs13194781 6.28E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_003522 HIST1H2BC 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs12206204 8.00E-07 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_003523 HIST1H2BC 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs12206204 8.00E-07 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_003525 HIST1H2BC 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs12206204 8.00E-07 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_003526 HIST1H2BC 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs12206204 8.00E-07 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_003529 HIST1H3E 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs10946808 4.00E-17 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003529 HIST1H3E 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10946808 6.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003529 HIST1H3E 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs10946808 6.00E-12 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_003530 HIST1H3E 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs10946808 4.00E-17 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003530 HIST1H3E 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10946808 6.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003530 HIST1H3E 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs10946808 6.00E-12 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_003531 HIST1H3E 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs10946808 4.00E-17 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003531 HIST1H3E 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10946808 6.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003531 HIST1H3E 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs10946808 6.00E-12 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_003532 HIST1H3E 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs10946808 4.00E-17 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003532 HIST1H3E 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10946808 6.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003532 HIST1H3E 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs10946808 6.00E-12 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_003533 HIST1H3E 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs10946808 4.00E-17 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003533 HIST1H3E 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10946808 6.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003533 HIST1H3E 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs10946808 6.00E-12 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_003534 HIST1H3E 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs10946808 4.00E-17 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003534 HIST1H3E 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10946808 6.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003534 HIST1H3E 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs10946808 6.00E-12 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_003535 HIST1H3E 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs10946808 4.00E-17 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003535 HIST1H3E 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10946808 6.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003535 HIST1H3E 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs10946808 6.00E-12 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_003536 HIST1H3E 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs10946808 4.00E-17 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003536 HIST1H3E 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10946808 6.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003536 HIST1H3E 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs10946808 6.00E-12 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_003537 HIST1H3E 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs10946808 4.00E-17 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003537 HIST1H3E 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10946808 6.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003537 HIST1H3E 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs10946808 6.00E-12 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_003550 MAD1L1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs6952808 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_003550 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11764337 3.86E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_003550 MAD1L1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4721135 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_003550 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4721295 2.21E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_003550 MAD1L1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs1107592 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_003550 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1107592 3.85E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_003550 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10224497 4.88E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_003550 MAD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs3800917 2.47E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_003558 PIP5K1B 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs4744712 8.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_003558 PIP5K1B 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10781329 8.34E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_003560 PLA2G6 19578365 http://www.ncbi.nlm.nih.gov/pubmed/19578365 Dysplastic Nevus Syndrome rs2284063 3.00E-08 Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. NHGRI|-1
NM_003560 PLA2G6 19578364 http://www.ncbi.nlm.nih.gov/pubmed/19578364 Melanoma rs2284063 2.00E-09 Genome-wide association study identifies three loci associated with melanoma risk. NHGRI|-1
NM_003560 PLA2G6 21478494 http://www.ncbi.nlm.nih.gov/pubmed/21478494 Cutaneous nevi rs738322 1.00E-06 Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk. NHGRI|-1
NM_003568 ANXA9 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs267734 1.00E-12 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_003574 VAPA 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7228911 6.74E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_003574 VAPA 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7228911 9.02E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_003576 STK24 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs9517320 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_003583 DYRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7980416 6.37E-05 NBL-GWAS version 2 dbGaP|2895
NM_003585 DOC2B 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs7217319 4.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_003587 DHX16 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130000 2.38E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_003591 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7920095 2.20E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003591 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7923172 1.43E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003591 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11595898 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003591 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934704 1.48E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003591 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1926554 3.32E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003591 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7099036 2.13E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003591 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934719 2.68E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003591 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003591 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003591 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003591 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2492448 3.84E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003591 CUL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11591754 1.68E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_003591 CUL2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs17582416 2.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_003599 SUPT3H 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs3799977 5.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_003599 SUPT3H 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs10948197 8.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_003599 SUPT3H 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs9395066 8.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003602 FKBP6 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17339199 4.21E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_003608 GPR65 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs8005161 4.00E-18 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_003615 SLC4A7 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs4973768 2.00E-08 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_003615 SLC4A7 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs4973768 6.00E-07 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_003617 RGS5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4657247 1.05E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_003617 RGS5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12566267 8.82E-06 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_003617 RGS5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4132246 4.90E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_003633 ENC1 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs16871023 1.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_003638 ITGA8 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs7077361 5.00E-06 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_003638 ITGA8 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Cholesterol rs7895372 6.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_003643 GCM1 20363506 http://www.ncbi.nlm.nih.gov/pubmed/20363506 Cardiovascular Diseases rs735860 4.00E-06 Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility. NHGRI|-1
NM_003646 DGKZ 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11038871 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_003648 DGKD 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs838705 9.00E-06 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_003652 CPZ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4696715 5.58E-07 NBL-GWAS version 2 dbGaP|2895
NM_003657 BCAS1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs290422 1.80E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_003661 APOL1 20668430 http://www.ncbi.nlm.nih.gov/pubmed/20668430 "Glomerulosclerosis, Focal Segmental" rs2239785 5.00E-13 A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. NHGRI|-1
NM_003664 AP3B1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2289599 2.99E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_003664 AP3B1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs5014235 1.96E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_003667 LGR5 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs1495377 7.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_003667 LGR5 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs4760790 4.00E-06 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_003667 LGR5 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7961581 1.00E-09 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_003667 LGR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7980195 5.47E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_003670 BHLHE40 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2616521 3.49E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_003682 MADD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs4752977 9.72E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_003682 MADD 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs7944584 2.00E-18 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_003687 PDLIM4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4594848 7.35E-05 NBL-GWAS version 2 dbGaP|2895
NM_003701 TNFSF11 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1325803 1.57E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_003701 TNFSF11 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs9533090 5.00E-25 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_003701 TNFSF11 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs9594738 2.00E-08 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_003701 TNFSF11 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs9594738 4.00E-06 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_003701 TNFSF11 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs9594759 2.00E-17 New sequence variants associated with bone mineral density. NHGRI|-1
NM_003701 TNFSF11 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs9594759 2.00E-21 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_003701 TNFSF11 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs2062305 5.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_003701 TNFSF11 21124946 http://www.ncbi.nlm.nih.gov/pubmed/21124946 Bone Density rs1021188 2.00E-14 Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone. NHGRI|-1
NM_003713 PPAP2B 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs17114036 4.00E-19 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_003713 PPAP2B 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs17114046 2.00E-07 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_003713 PPAP2B 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1930762 3.92E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_003714 STC2 19165155 http://www.ncbi.nlm.nih.gov/pubmed/19165155 Adiponectin rs7722022 9.00E-06 Genome-wide linkage and association analyses to identify genes influencing adiponectin levels: the GEMS Study. NHGRI|-1
NM_003714 STC2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs889014 9.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_003716 CADPS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs304230 1.40E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_003719 PDE8B 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs4457053 3.00E-12 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_003721 RFXANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10896 1.65E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_003722 TP63 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs4488809 7.00E-26 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_003722 TP63 20871597 http://www.ncbi.nlm.nih.gov/pubmed/20871597 Lung Neoplasms rs10937405 7.00E-12 Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations. NHGRI|-1
NM_003722 TP63 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1515496 8.68E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003722 TP63 18794855 http://www.ncbi.nlm.nih.gov/pubmed/18794855 Urinary Bladder Neoplasms rs710521 1.00E-07 Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_003722 TP63 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs710521 2.00E-10 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_003722 TP63 20348956 http://www.ncbi.nlm.nih.gov/pubmed/20348956 Urinary Bladder Neoplasms rs710521 6.00E-08 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_003725 HSD17B6 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs12367822 1.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_003726 SKAP1 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs2084881 2.00E-06 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_003726 SKAP1 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs9303542 1.00E-06 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_003730 RNASET2 20526339 http://www.ncbi.nlm.nih.gov/pubmed/20526339 Vitiligo rs2236313 1.00E-16 Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. NHGRI|-1
NM_003733 OASL 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7957197 2.00E-08 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_003741 CHRD 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs3930234 8.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_003742 ABCB11 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs569805 9.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_003742 ABCB11 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs552976 8.00E-18 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_003742 ABCB11 18521185 http://www.ncbi.nlm.nih.gov/pubmed/18521185 Blood Glucose rs563694 4.00E-07 Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels. NHGRI|-1
NM_003742 ABCB11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs563694 1.17E-07 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_003743 NCOA1 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs2165738 4.00E-06 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_003744 NUMB 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Atherosclerosis rs10483853 6.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_003747 TNKS 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs9644708 3.44E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_003747 TNKS 19557161 http://www.ncbi.nlm.nih.gov/pubmed/19557161 Adiposity rs545854 9.00E-09 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. NHGRI|-1
NM_003747 TNKS 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs545854 3.57E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_003747 TNKS 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs9987289 3.00E-13 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_003747 TNKS 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs9987289 1.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_003747 TNKS 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs9987289 4.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_003747 TNKS 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs6601299 1.00E-08 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_003747 TNKS 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs2126259 7.00E-12 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_003747 TNKS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9329191 6.16E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_003749 IRS2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4773094 7.81E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1041466 3.67E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1041466 4.00E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1411766 1.82E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1411766 8.15E-06 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17412858 2.11E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17412858 9.68E-06 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6492208 2.03E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6492208 7.41E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2391777 1.12E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2391777 3.42E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2391778 2.08E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2391778 8.33E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9515085 1.40E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9515085 4.40E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1411765 2.01E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1411765 8.24E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7989848 4.14E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7989848 7.02E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1929210 3.77E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9521445 1.21E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_003749 IRS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9521445 2.95E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003754 EIF3F 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs12420464 3.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_003756 EIF3H 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs4876662 2.00E-06 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_003756 EIF3H 18372905 http://www.ncbi.nlm.nih.gov/pubmed/18372905 Colorectal Neoplasms rs16892766 3.00E-18 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. NHGRI|-1
NM_003772 JRKL 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs11212364 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_003772 JRKL 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1960997 9.62E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_003772 JRKL 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs2405657 3.00E-06 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_003772 JRKL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2155907 4.02E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_003772 JRKL 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2509843 2.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_003772 JRKL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2509843 4.70E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_003772 JRKL 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs4237591 2.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_003773 HYAL2 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs11130248 5.00E-07 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_003777 DNAH11 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs12670798 6.00E-09 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_003777 DNAH11 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs12670798 9.00E-07 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_003777 DNAH11 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs368331 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_003777 DNAH11 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs368331 4.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_003777 DNAH11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4722063 4.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_003783 B3GALT2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7554157 3.35E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_003787 NOL4 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs7239368 9.00E-06 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_003787 NOL4 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs1013696 4.00E-06 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_003793 CTSF 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs2242663 1.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_003796 C19orf2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs184583 2.90E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_003796 C19orf2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs184583 3.72E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_003800 RNGTT 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Vitamin D rs10485165 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_003800 RNGTT 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, LDL" rs12527253 1.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_003805 CRADD 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs3825199 2.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003805 CRADD 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs11107116 6.00E-10 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_003820 TNFRSF14 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs734999 3.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_003821 RIPK2 20018961 http://www.ncbi.nlm.nih.gov/pubmed/20018961 Leprosy rs42490 1.00E-16 Genomewide association study of leprosy. NHGRI|-1
NM_003821 RIPK2 20018961 http://www.ncbi.nlm.nih.gov/pubmed/20018961 Leprosy rs40457 1.00E-12 Genomewide association study of leprosy. NHGRI|-1
NM_003821 RIPK2 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs160441 8.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2737621 3.42E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs60636333 1.48E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs60636333 2.64E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs3790844 2.45E-10 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003822 NR5A2 20101243 http://www.ncbi.nlm.nih.gov/pubmed/20101243 Pancreatic Neoplasms rs3790844 2.00E-10 "A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33." NHGRI|-1
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs3790843 6.69E-09 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2821367 1.89E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs3828112 3.78E-05 NBL-GWAS version 2 dbGaP|2895
NM_003822 NR5A2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs16844716 9.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17664308 1.48E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003822 NR5A2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2363451 6.17E-07 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12029406 1.04E-07 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4465241 4.79E-07 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10919791 6.37E-10 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4244145 1.98E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2816939 9.58E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003822 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2821347 1.16E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003823 RTEL1 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs6010620 2.00E-09 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_003823 RTEL1 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs6010620 3.00E-12 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_003823 RTEL1 19578366 http://www.ncbi.nlm.nih.gov/pubmed/19578366 Glioma rs6010620 3.00E-09 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. NHGRI|-1
NM_003823 RTEL1 19578366 http://www.ncbi.nlm.nih.gov/pubmed/19578366 Glioma rs4809324 2.00E-09 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. NHGRI|-1
NM_003823 RTEL1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2297441 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_003829 MPDZ 19754311 http://www.ncbi.nlm.nih.gov/pubmed/19754311 Acquired Immunodeficiency Syndrome rs1360517 3.00E-06 Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). NHGRI|-1
NM_003835 RGS9 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs8068707 2.40E-06 NBL-GWAS version 1 dbGaP|2845
NM_003836 DLK1 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Optic Disk rs1884537 2.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_003836 DLK1 21573907 http://www.ncbi.nlm.nih.gov/pubmed/21573907 "Diabetes Mellitus, Type 2" rs730570 8.00E-06 "Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas." NHGRI|-1
NM_003837 FBP2 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs16910061 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_003839 TNFRSF11A 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs884205 9.00E-09 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_003839 TNFRSF11A 20436471 http://www.ncbi.nlm.nih.gov/pubmed/20436471 Osteitis Deformans rs2957128 2.00E-11 "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone." NHGRI|-1
NM_003839 TNFRSF11A 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs3018362 1.00E-06 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_003839 TNFRSF11A 20436471 http://www.ncbi.nlm.nih.gov/pubmed/20436471 Osteitis Deformans rs3018362 5.00E-13 "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone." NHGRI|-1
NM_003839 TNFRSF11A 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs3018362 8.00E-21 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_003847 PEX11A 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs17816376 2.03E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_003848 SUCLG2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4417811 1.52E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_003852 TRIM24 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Weight rs1874326 9.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_003853 IL18RAP 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs2058660 2.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_003853 IL18RAP 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs917997 1.00E-15 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_003854 IL1RL2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1922294 6.63E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_003855 IL18R1 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs3771166 3.00E-09 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_003855 IL18R1 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs13015714 4.00E-09 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_003856 IL1RL1 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Eosinophils rs1420101 5.00E-14 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_003856 IL1RL1 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs13015714 4.00E-09 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_003862 FGF18 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Blood Pressure rs254893 6.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_003866 INPP4B 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs17007695 9.00E-07 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_003872 NRP2 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs7603514 8.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_003873 NRP1 21682944 http://www.ncbi.nlm.nih.gov/pubmed/21682944 Schizophrenia rs1412115 6.00E-06 DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population. NHGRI|-1
NM_003877 SOCS2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs3825199 2.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003877 SOCS2 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs11107116 6.00E-10 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_003879 CFLAR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12621441 3.43E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_003887 ASAP2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1109670 9.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_003888 ALDH1A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs597804 5.59E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003888 ALDH1A2 19609347 http://www.ncbi.nlm.nih.gov/pubmed/19609347 Hypertension rs1550576 3.00E-06 A genome-wide association study of hypertension and blood pressure in African Americans. NHGRI|-1
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3129975 2.40E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs12526186 1.27E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_003897 IER3 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs12526186 3.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_003897 IER3 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs6911628 2.20E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs4711229 5.43E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs3131043 1.76E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3131043 1.81E-11 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs34682678 1.68E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9295917 5.09E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs13198118 2.07E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264362 1.31E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003897 IER3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs886424 4.70E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9295924 2.69E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs4713380 6.51E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs915664 8.45E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003897 IER3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1264350 1.86E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7749924 2.25E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2535331 3.74E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2250264 8.16E-09 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003897 IER3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2844659 1.23E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2535327 1.30E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844654 4.43E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264333 4.42E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264332 4.98E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264331 4.47E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_003897 IER3 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs7756521 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_003897 IER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7756521 7.58E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_003899 ARHGEF7 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs4773330 8.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_003900 SQSTM1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10516140 6.02E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_003904 ZNF259 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs964184 1.00E-12 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_003904 ZNF259 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs964184 1.00E-17 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_003904 ZNF259 20657596 http://www.ncbi.nlm.nih.gov/pubmed/20657596 Hypertriglyceridemia rs964184 5.00E-24 Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. NHGRI|-1
NM_003904 ZNF259 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs964184 2.00E-11 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_003904 ZNF259 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs964184 4.00E-62 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_003904 ZNF259 21729881 http://www.ncbi.nlm.nih.gov/pubmed/21729881 Vitamin E rs964184 8.00E-12 Genome-wide association study identifies common variants associated with circulating vitamin E levels NHGRI|-1
NM_003904 ZNF259 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs11823543 3.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_003904 ZNF259 20442857 http://www.ncbi.nlm.nih.gov/pubmed/20442857 1-Alkyl-2-acetylglycerophosphocholine Esterase rs12286037 4.00E-08 Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study. NHGRI|-1
NM_003904 ZNF259 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs12286037 1.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_003904 ZNF259 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs12286037 1.00E-26 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_003904 ZNF259 18179892 http://www.ncbi.nlm.nih.gov/pubmed/18179892 "Cholesterol, LDL" rs6589566 3.00E-11 Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. NHGRI|-1
NM_003904 ZNF259 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs2075290 2.00E-14 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_003904 ZNF259 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2075290 1.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_003904 ZNF259 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2075290 2.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_003904 ZNF259 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs2266788 5.00E-13 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_003904 ZNF259 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2266788 2.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_003904 ZNF259 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2266788 2.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_003904 ZNF259 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2266788 4.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_003916 AP1S2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs798159 4.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_003917 AP1G2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs2281680 6.00E-08 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_003924 PHOX2B 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs16853571 5.59E-07 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_003927 MBD2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs1039189 4.33E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_003929 RAB7L1 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson Disease rs947211 2.00E-12 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_003930 SKAP2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs7804356 5.00E-09 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_003933 BAIAP3 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4984814 2.79E-08 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_003934 FUBP3 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs7466269 3.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_003934 FUBP3 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs7466269 8.00E-07 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_003937 KYNU 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs352892 5.04E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_003937 KYNU 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2890652 1.00E-10 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_003938 AP3D1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Mass Index rs3803915 5.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_003942 RPS6KA4 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs538147 2.00E-10 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_003953 MPZL1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs12757250 9.23E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_003956 CH25H 21041692 http://www.ncbi.nlm.nih.gov/pubmed/21041692 Heart Function Tests rs1937332 7.00E-07 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. NHGRI|-1
NM_003956 CH25H 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs11203032 8.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_003960 NAT8 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs13538 5.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_003965 CCRL2 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs1015164 9.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_003965 CCRL2 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs6441975 5.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_003966 SEMA5A 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7702187 7.12E-06 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_003966 SEMA5A 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7702187 8.00E-06 High-resolution whole-genome association study of Parkinson disease. NHGRI|-1
NM_003966 SEMA5A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs436243 4.05E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_003966 SEMA5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs2388004 6.00E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_003970 MYOM2 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs641525 5.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_003972 BTAF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11186792 6.28E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_003974 DOK2 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs17581368 7.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_003977 AIP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs601363 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_003977 AIP 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4084113 5.09E-07 NBL-GWAS version 1 dbGaP|2845
NM_003977 AIP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7124630 4.90E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_003979 GPRC5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1056927 7.24E-05 NBL-GWAS version 2 dbGaP|2895
NM_003979 GPRC5A 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs704225 6.66E-06 NBL-GWAS version 1 dbGaP|2845
NM_003981 PRC1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs8042680 2.00E-10 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_003987 PAX2 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs4509693 6.00E-06 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_003988 PAX2 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs4509693 6.00E-06 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_003989 PAX2 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs4509693 6.00E-06 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_003990 PAX2 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs4509693 6.00E-06 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_003991 EDNRB 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs9574199 7.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_003991 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6563036 6.86E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003991 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7996252 2.72E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003991 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7996252 8.44E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_003991 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2248525 3.14E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_003991 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2248525 8.12E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_003991 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2265775 5.77E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_003991 EDNRB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2987526 3.23E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_003994 KITLG 19483681 http://www.ncbi.nlm.nih.gov/pubmed/19483681 Testicular Neoplasms rs995030 1.00E-31 A genome-wide association study of testicular germ cell tumor. NHGRI|-1
NM_003994 KITLG 19483681 http://www.ncbi.nlm.nih.gov/pubmed/19483681 Testicular Neoplasms rs995030 3.00E-30 A genome-wide association study of testicular germ cell tumor. NHGRI|-1
NM_003994 KITLG 20543847 http://www.ncbi.nlm.nih.gov/pubmed/20543847 Testicular Neoplasms rs3782181 2.00E-26 "Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer." NHGRI|-1
NM_003994 KITLG 19483682 http://www.ncbi.nlm.nih.gov/pubmed/19483682 Testicular Neoplasms rs4474514 6.00E-15 Common variation in KITLG and at 5q31.3 predisposes to testicular germ cell cancer. NHGRI|-1
NM_003994 KITLG 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Hair Color rs12821256 4.00E-30 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_003994 KITLG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7960664 9.96E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_003998 NFKB1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs7665090 4.00E-12 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_004000 CHI3L2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17654531 1.16E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_004006 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004006 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004007 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004007 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004009 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004009 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004010 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004010 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004011 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004011 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004012 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004012 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004013 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004013 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004014 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004014 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004015 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004015 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004016 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004016 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004017 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004017 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004018 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004018 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004019 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004019 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004020 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004020 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004021 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004021 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004022 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004022 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004023 DMD 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10521979 5.16E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004023 DMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6527185 3.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004028 AQP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs9653034 3.06E-05 NBL-GWAS version 2 dbGaP|2895
NM_004028 AQP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs8083994 2.35E-05 NBL-GWAS version 2 dbGaP|2895
NM_004036 ADCY3 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs713586 6.00E-22 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_004040 RHOB 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs13021401 3.00E-06 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_004052 BNIP3 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs7098827 3.40E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_004055 CAPN5 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs3781684 7.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_004056 CA8 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs3110127 4.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_004056 CA8 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs6995588 2.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_004060 CCNG1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17061327 6.05E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004061 CDH12 19557197 http://www.ncbi.nlm.nih.gov/pubmed/19557197 Waist Circumference rs4701252 2.00E-06 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. NHGRI|-1
NM_004061 CDH12 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2551492 6.15E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004061 CDH12 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2551493 5.70E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004061 CDH12 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2260217 6.15E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004061 CDH12 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1911964 4.88E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004061 CDH12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs17358685 7.51E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_004061 CDH12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs9292991 2.23E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_004067 CHN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs39059 5.91E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_004072 CMKLR1 21483023 http://www.ncbi.nlm.nih.gov/pubmed/21483023 Response to platinum-based chemotherapy in non-small-cell lung cancer rs1878022 5.00E-07 Genome-wide association study of survival in non-small cell lung cancer patients receiving platinum-based chemotherapy. NHGRI|-1
NM_004072 CMKLR1 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs10861905 8.00E-07 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_004080 DGKB 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs6971925 3.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_004084 DEFA1 21151130 http://www.ncbi.nlm.nih.gov/pubmed/21151130 Endometriosis rs2738113 3.00E-07 Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. NHGRI|-1
NM_004098 EMX2 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs2184898 3.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_004100 EYA4 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 alpha-Macroglobulins rs9402515 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_004100 EYA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs9402515 8.86E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_004100 EYA4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4487594 1.06E-06 NBL-GWAS version 1 dbGaP|2845
NM_004100 EYA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4487594 2.88E-06 NBL-GWAS version 2 dbGaP|2895
NM_004101 F2RL2 20068591 http://www.ncbi.nlm.nih.gov/pubmed/20068591 Hearing Loss rs457717 4.00E-07 A genome-wide association study for age-related hearing impairment in the Saami. NHGRI|-1
NM_004103 PTK2B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7833348 7.55E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_004105 EFEMP1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs3791679 6.00E-11 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_004105 EFEMP1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs3791679 6.00E-09 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_004105 EFEMP1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs3791675 2.00E-12 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_004105 EFEMP1 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Body Height rs3791675 2.00E-09 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_004105 EFEMP1 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs3791675 3.00E-07 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_004105 EFEMP1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs3791675 4.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_004105 EFEMP1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs6751715 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_004105 EFEMP1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs7577894 1.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_004113 FGF12 21139019 http://www.ncbi.nlm.nih.gov/pubmed/21139019 Carcinoid Tumor rs975121 7.00E-06 A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum. NHGRI|-1
NM_004113 FGF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs9859577 9.87E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_004113 FGF12 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Phosphatidylcholines rs4453795 4.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_004113 FGF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2886785 9.60E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_004113 FGF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9873551 5.37E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_004113 FGF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6444558 1.54E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_004113 FGF12 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7635839 3.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_004122 GHSR 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs572169 3.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_004128 GTF2F2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7336303 7.84E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_004131 GZMB 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs8192917 3.00E-08 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_004131 GZMB 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs854384 1.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_004132 HABP2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4265536 8.64E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_004133 HNF4G 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1805100 7.60E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_004133 HNF4G 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2922763 6.00E-08 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_004133 HNF4G 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1531462 7.20E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_004133 HNF4G 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs16939284 5.86E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_004133 HNF4G 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs16939046 4.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_004136 IREB2 20173748 http://www.ncbi.nlm.nih.gov/pubmed/20173748 "Pulmonary Disease, Chronic Obstructive" rs13180 2.00E-08 Variants in FAM13A are associated with chronic obstructive pulmonary disease. NHGRI|-1
NM_004137 KCNMB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17673653 9.07E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_004159 PSMB8 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 "Glomerulonephritis, IGA" rs9357155 2.00E-12 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_004159 PSMB8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2071540 1.26E-69 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004163 RAB27B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2311120 2.14E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_004174 SLC9A3 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs4957048 1.00E-09 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_004174 SLC9A3 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs11739663 3.00E-08 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_004176 SREBF1 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs11868035 6.00E-08 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_004180 TANK 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs10192369 9.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_004180 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6432628 9.13E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_004180 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13034284 1.85E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_004180 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9967749 8.13E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_004180 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11681327 4.77E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_004180 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7603576 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_004180 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2551691 9.03E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_004180 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs197275 4.42E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_004183 BEST1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2668898 5.65E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_004188 GFI1B 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs2905072 6.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_004189 SOX14 19578179 http://www.ncbi.nlm.nih.gov/pubmed/19578179 Acenocoumarol rs10935268 8.00E-07 A genome-wide association study of acenocoumarol maintenance dosage. NHGRI|-1
NM_004197 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs416002 9.33E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_004197 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs389884 8.47E-87 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004197 STK19 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs389884 2.08E-18 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_004197 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs389884 9.42E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_004197 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs387608 1.91E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_004197 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs387608 6.95E-09 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_004197 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs389883 1.56E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_004197 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs389512 2.34E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_004197 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs389512 9.00E-09 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_004199 P4HA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4594848 7.35E-05 NBL-GWAS version 2 dbGaP|2895
NM_004203 PKMYT1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs886427 6.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_004210 NEURL 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7071247 2.00E-07 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_004211 SLC6A5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2276432 1.38E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_004211 SLC6A5 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs7128311 5.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_004212 SLC28A2 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs2453533 5.00E-22 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_004218 RAB11B 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs2967605 1.00E-08 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_004219 PTTG1 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs2431697 2.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_004219 PTTG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs883517 5.94E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_004219 PTTG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12514981 7.68E-05 NBL-GWAS version 2 dbGaP|2895
NM_004224 GPR50 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6627154 7.13E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_004224 GPR50 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs5969786 7.52E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_004225 MFHAS1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs332034 6.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_004226 STK17B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs13001220 2.99E-05 NBL-GWAS version 2 dbGaP|2895
NM_004226 STK17B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4850679 5.83E-05 NBL-GWAS version 2 dbGaP|2895
NM_004233 CD83 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2094923 2.89E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_004233 CD83 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2274822 1.56E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_004233 CD83 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs6914079 2.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_004233 CD83 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs7770731 1.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_004233 CD83 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs6941421 6.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_004233 CD83 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12333130 5.60E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_004233 CD83 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1003024 6.43E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_004233 CD83 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs1003024 7.51E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_004233 CD83 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1555051 7.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_004233 CD83 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs7750009 7.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_004235 KLF4 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs817858 7.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_004239 TRIP11 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs8007661 6.00E-10 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_004239 TRIP11 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs7153027 1.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_004241 JMJD1C 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs12355784 5.00E-10 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_004241 JMJD1C 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs2393967 3.00E-21 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_004241 JMJD1C 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs2893923 5.00E-08 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_004241 JMJD1C 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs10761779 7.00E-10 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_004244 CD163 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Creatine Kinase rs7136716 3.00E-26 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_004245 TGM5 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs748404 1.00E-06 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_004248 PRLHR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11198446 7.49E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_004255 COX5A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4886642 1.58E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004257 TGFBRAP1 19754311 http://www.ncbi.nlm.nih.gov/pubmed/19754311 Acquired Immunodeficiency Syndrome rs1020064 7.00E-06 Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). NHGRI|-1
NM_004265 FADS2 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, HDL" rs174570 4.00E-06 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_004265 FADS2 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs174570 4.00E-13 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_004265 FADS2 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs174570 2.00E-10 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_004265 FADS2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs1535 4.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_004265 FADS2 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, HDL" rs1535 7.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_004265 FADS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs1535 1.16E-05 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_004265 FADS2 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs174583 3.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_004267 CHST2 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs894177 3.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_004271 LY86 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs2326810 7.00E-06 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_004271 LY86 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs1294421 2.00E-17 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_004272 HOMER1 18193045 http://www.ncbi.nlm.nih.gov/pubmed/18193045 Body Height rs10078095 3.00E-06 Common variants in the GDF5-UQCC region are associated with variation in human height. NHGRI|-1
NM_004273 CHST3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4148912 8.01E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_004274 AKAP6 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs2383378 6.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_004281 BAG3 21459883 http://www.ncbi.nlm.nih.gov/pubmed/21459883 "Cardiomyopathy, Dilated" rs2234962 4.00E-12 A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. NHGRI|-1
NM_004281 BAG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs2234962 9.62E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_004284 CHD1L 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Hemoglobins rs4950322 7.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_004284 CHD1L 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Resistin rs4950322 2.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_004287 GOSR2 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs17608766 5.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_004289 NFE2L3 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs1055144 1.00E-24 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_004289 NFE2L3 21151130 http://www.ncbi.nlm.nih.gov/pubmed/21151130 Endometriosis rs12700667 1.00E-09 Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis. NHGRI|-1
NM_004290 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs252139 7.04E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004290 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs252095 4.58E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004290 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs409037 4.58E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004293 GDA 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs11143230 7.00E-06 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_004293 GDA 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs11143230 8.00E-07 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_004296 RGS6 20811658 http://www.ncbi.nlm.nih.gov/pubmed/20811658 Smoking Cessation rs7159300 4.00E-06 Genome-wide association for smoking cessation success in a trial of precessation nicotine replacement. NHGRI|-1
NM_004296 RGS6 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4903031 5.00E-06 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_004304 ALK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs3923028 3.80E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_004305 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs12989701 3.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_004305 BIN1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs7561528 4.00E-14 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_004305 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs744373 1.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_004305 BIN1 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs744373 2.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_004305 BIN1 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs744373 3.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_004305 BIN1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs13418717 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_004306 ANXA13 21046636 http://www.ncbi.nlm.nih.gov/pubmed/21046636 Brain Waves rs2294015 9.00E-06 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. NHGRI|-1
NM_004306 ANXA13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs2294015 5.83E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_004306 ANXA13 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs10088262 4.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_004308 ARHGAP1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7932354 4.00E-09 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_004316 ASCL1 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs10745954 2.00E-11 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_004316 ASCL1 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs10778213 1.00E-10 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_004318 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900493 6.94E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004318 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483170 5.79E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004318 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483172 6.77E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004321 KIF1A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs755300 2.88E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_004321 KIF1A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4613 4.40E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_004321 KIF1A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4456706 2.60E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_004326 BCL9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2000072 5.54E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004327 BCR 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs5751614 6.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_004337 OSGIN2 20018961 http://www.ncbi.nlm.nih.gov/pubmed/20018961 Leprosy rs40457 1.00E-12 Genomewide association study of leprosy. NHGRI|-1
NM_004338 C18orf1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6505798 8.21E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_004342 CALD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12539126 8.96E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004342 CALD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10488456 6.08E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004348 RUNX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4714860 7.86E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_004350 RUNX3 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs11249215 9.00E-11 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_004350 RUNX3 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs10903122 2.00E-10 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_004358 CDC25B 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Bipolar Disorder rs3761218 7.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_004360 CDH1 19011631 http://www.ncbi.nlm.nih.gov/pubmed/19011631 Colorectal Neoplasms rs9929218 1.00E-08 Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. NHGRI|-1
NM_004361 CDH7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17074003 4.56E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_004361 CDH7 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs8083346 6.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_004361 CDH7 21041692 http://www.ncbi.nlm.nih.gov/pubmed/21041692 Heart Function Tests rs470490 5.00E-06 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. NHGRI|-1
NM_004362 CLGN 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Bilirubin rs1594468 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_004364 CEBPA 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory Bowel Diseases rs10500264 4.00E-10 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_004364 CEBPA 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs736289 9.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_004365 CETN3 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs10037512 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_004365 CETN3 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1366594 1.00E-13 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_004365 CETN3 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs1366594 1.00E-07 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_004365 CETN3 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs1366594 8.00E-10 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_004365 CETN3 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs12518099 7.00E-07 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_004365 CETN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2972956 6.07E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_004367 CCR6 20453841 http://www.ncbi.nlm.nih.gov/pubmed/20453841 "Arthritis, Rheumatoid" rs3093024 8.00E-19 A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. NHGRI|-1
NM_004367 CCR6 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs3093023 2.00E-11 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_004377 CPT1B 18820697 http://www.ncbi.nlm.nih.gov/pubmed/18820697 Narcolepsy rs5770917 6.00E-08 Variant between CPT1B and CHKB associated with susceptibility to narcolepsy. NHGRI|-1
NM_004382 CRHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1635291 2.27E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_004382 CRHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7215239 3.43E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_004382 CRHR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1724425 7.77E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_004382 CRHR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs9303521 1.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_004382 CRHR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs9303521 4.00E-06 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_004383 CSK 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs1378942 1.00E-23 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_004385 VCAN 20516156 http://www.ncbi.nlm.nih.gov/pubmed/20516156 "Depressive Disorder, Major" rs310501 7.00E-06 Genome-wide association study of major recurrent depression in the U.K. population. NHGRI|-1
NM_004386 NCAN 21353194 http://www.ncbi.nlm.nih.gov/pubmed/21353194 Bipolar Disorder rs1064395 2.00E-09 Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. NHGRI|-1
NM_004389 CTNNA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12471455 9.45E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_004389 CTNNA2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Interleukin-10 rs11695685 5.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_004389 CTNNA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13423141 8.74E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_004389 CTNNA2 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs13409348 3.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_004389 CTNNA2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs399885 5.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_004389 CTNNA2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs7570469 6.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_004390 CTSH 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs3825932 3.00E-15 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_004390 CTSH 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs3825932 8.00E-08 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_004392 DACH1 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Cystatin C rs626277 3.00E-11 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_004392 DACH1 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs9572423 9.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_004392 DACH1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7317253 2.51E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_004392 DACH1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs9592783 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_004394 DAP 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs267939 6.00E-12 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_004394 DAP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17176973 2.27E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_004397 DDX6 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs6421571 3.00E-12 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_004397 DDX6 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs4639966 1.00E-16 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_004397 DDX6 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs10892279 1.00E-12 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_004406 DMBT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7902878 9.49E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_004408 DNM1 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2502731 2.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_004413 DPEP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs154659 7.56E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_004413 DPEP1 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs154659 7.00E-08 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_004432 ELAVL2 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs4246856 6.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_004432 ELAVL2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Weight rs2225614 3.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_004432 ELAVL2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10491833 5.28E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_004432 ELAVL2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9406815 9.13E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_004432 ELAVL2 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs12552736 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_004432 ELAVL2 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs13300284 4.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_004432 ELAVL2 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs17774966 8.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_004432 ELAVL2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Waist Circumference rs613391 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_004432 ELAVL2 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Stomach Neoplasms rs10811771 8.00E-07 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_004433 ELF3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4436440 5.16E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_004433 ELF3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10800812 1.62E-08 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_004433 ELF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2819358 1.39E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_004434 EML1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4905898 5.84E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_004434 EML1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs10141863 3.75E-06 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_004434 EML1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs12891247 6.53E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_004438 EPHA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs3935261 6.78E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_004438 EPHA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs10804287 3.64E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_004438 EPHA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs897144 2.13E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_004438 EPHA4 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 "Ventricular Function, Left" rs10498091 6.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_004438 EPHA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17431881 1.75E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_004440 EPHA7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs625822 7.50E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_004440 EPHA7 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs594442 1.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_004440 EPHA7 21647738 http://www.ncbi.nlm.nih.gov/pubmed/21647738 C-Reactive Protein rs1408282 1.00E-06 Genome-wide Association with C-Reactive Protein Levels in CLHNS: Evidence for the CRP and HNF1A Loci and their Interaction with Exposure to a Pathogenic Environment. NHGRI|-1
NM_004441 EPHB1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs823968 6.68E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_004443 EPHB3 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs3930234 8.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_004447 EPS8 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Ferritins rs17415853 7.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_004449 ERG 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs7275212 2.00E-18 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_004449 ERG 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2836496 7.04E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004449 ERG 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2836505 5.78E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004449 ERG 20662065 http://www.ncbi.nlm.nih.gov/pubmed/20662065 Lupus Vulgaris rs743446 5.00E-06 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. NHGRI|-1
NM_004452 ESRRB 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Attention Deficit Disorder with Hyperactivity rs2360997 8.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_004454 ETV5 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs7647305 7.00E-11 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_004454 ETV5 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7647305 4.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_004454 ETV5 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs9816226 2.00E-18 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_004454 ETV5 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Attention Deficit Disorder with Hyperactivity rs10049246 8.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_004462 FDFT1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs2645424 3.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_004462 FDFT1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs2645424 7.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_004464 FGF5 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs16998073 1.00E-21 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_004465 FGF10 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs4415084 8.00E-11 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_004465 FGF10 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs4296809 9.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_004466 GPC5 21441931 http://www.ncbi.nlm.nih.gov/pubmed/21441931 Nephrotic Syndrome rs16946160 3.00E-07 Common variation in GPC5 is associated with acquired nephrotic syndrome. NHGRI|-1
NM_004466 GPC5 20304703 http://www.ncbi.nlm.nih.gov/pubmed/20304703 Lung Neoplasms rs2352028 6.00E-06 Genetic variants and risk of lung cancer in never smokers: a genome-wide association study. NHGRI|-1
NM_004466 GPC5 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs1413191 5.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_004466 GPC5 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Docosahexaenoic Acids rs17267292 1.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_004466 GPC5 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs9523762 1.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_004466 GPC5 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs9523762 7.00E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_004466 GPC5 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs8002779 3.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_004473 FOXE1 19198613 http://www.ncbi.nlm.nih.gov/pubmed/19198613 Thyroid Neoplasms rs965513 2.00E-27 Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. NHGRI|-1
NM_004476 FOLH1B 20801717 http://www.ncbi.nlm.nih.gov/pubmed/20801717 Amyotrophic Lateral Sclerosis rs1488902 3.00E-06 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. NHGRI|-1
NM_004477 FRG1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs1451213 5.84E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_004480 FUT8 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1256531 4.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_004481 GALNT2 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs2144300 3.00E-14 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_004481 GALNT2 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs2144300 8.00E-07 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_004481 GALNT2 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, HDL" rs4846914 2.00E-13 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_004481 GALNT2 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs4846914 4.00E-08 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_004481 GALNT2 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs4846914 7.00E-15 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_004481 GALNT2 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs10489615 4.00E-09 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_004482 GALNT3 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs6710518 5.00E-10 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_004485 GNG4 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Menopause rs291353 6.00E-06 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_004490 GRB14 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs10195252 4.00E-34 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_004490 GRB14 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10189532 3.39E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_004490 GRB14 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs16849225 4.00E-11 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_004495 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_004495 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_004495 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_004495 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_004495 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_004495 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_004500 HNRNPC 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8016099 3.74E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_004500 HNRNPC 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs17197037 2.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_004501 HNRNPU 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4658673 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_004506 HSF2 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs9398652 4.00E-15 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_004506 HSF2 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Heart Rate rs12110693 2.00E-09 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_004513 IL16 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs7172689 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_004520 KIF2A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2030889 6.48E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_004520 KIF2A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6449558 7.12E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_004522 KIF5C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7577450 8.32E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_004522 KIF5C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10929935 7.26E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_004522 KIF5C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs10929935 5.43E-04 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_004523 KIF11 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs6583826 7.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_004525 LRP2 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs830998 9.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_004525 LRP2 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Uric Acid rs2544390 4.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_004528 MGST3 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs6686643 7.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_004538 NAP1L3 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4893039 1.81E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_004538 NAP1L3 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs5983240 5.13E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_004540 NCAM2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs12483298 1.37E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004540 NCAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4605456 8.79E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_004540 NCAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs8127865 5.20E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_004540 NCAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2218433 6.96E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_004540 NCAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7279496 8.95E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_004540 NCAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs8126935 7.53E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_004540 NCAM2 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs11088859 4.00E-08 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_004540 NCAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2826803 8.21E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_004540 NCAM2 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs2826891 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_004540 NCAM2 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs2827312 8.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_004544 NDUFA10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11674512 1.59E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_004544 NDUFA10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs11695034 1.06E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_004554 NFATC4 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs1950500 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs8192583 2.25E-20 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3134942 1.92E-85 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3134942 1.86E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2071277 1.58E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2071277 8.14E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3131296 5.53E-85 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3131296 1.09E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_004557 NOTCH4 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3131296 4.44E-14 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_004557 NOTCH4 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs3131296 2.00E-10 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs79788880 4.00E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130292 9.10E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_004557 NOTCH4 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3131294 4.04E-32 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs206015 7.69E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs8192591 3.40E-24 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs394657 1.04E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs394657 1.53E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs422951 2.31E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs422951 3.28E-07 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8192584 9.96E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3132946 4.92E-126 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs443198 1.53E-11 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs434841 3.80E-96 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs377763 9.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_004557 NOTCH4 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs377763 1.50E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_004557 NOTCH4 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3134926 1.16E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3130299 1.19E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004557 NOTCH4 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3115576 2.29E-10 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_004557 NOTCH4 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6936204 2.98E-22 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_004557 NOTCH4 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9267971 4.79E-12 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_004557 NOTCH4 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130311 1.54E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_004557 NOTCH4 20595679 http://www.ncbi.nlm.nih.gov/pubmed/20595679 "Glomerulonephritis, IGA" rs3115573 1.00E-09 HLA has strongest association with IgA nephropathy in genome-wide analysis. NHGRI|-1
NM_004557 NOTCH4 21505073 http://www.ncbi.nlm.nih.gov/pubmed/21505073 "Arthritis, Rheumatoid" rs9296015 2.00E-38 The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population. NHGRI|-1
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs6916062 2.52E-22 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9267992 2.98E-161 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004557 NOTCH4 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs3130320 3.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9268005 6.93E-161 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004557 NOTCH4 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs3130340 1.00E-07 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_004557 NOTCH4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs926070 3.19E-161 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004560 ROR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1591068 8.21E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_004560 ROR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1855065 4.28E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_004561 OVOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7114014 2.27E-05 NBL-GWAS version 2 dbGaP|2895
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9458255 9.49E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs992421 1.56E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs10755582 2.69E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6937817 1.71E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs12191995 7.53E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs17651062 1.03E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Lysine rs992037 1.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3019442 7.57E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3016563 5.39E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3016562 5.39E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9458363 1.15E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3019433 6.37E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3016557 2.75E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs3016539 7.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2022991 1.31E-22 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9365344 1.11E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1105056 3.72E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9456734 7.45E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9295184 3.26E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2846494 1.18E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2846488 3.07E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4636000 3.41E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2155510 6.56E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1012424 1.22E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9458611 5.98E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004562 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2803059 9.79E-13 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_004564 PET112L 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs360929 9.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_004565 PEX14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2480775 3.09E-05 NBL-GWAS version 2 dbGaP|2895
NM_004565 PEX14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10864463 9.93E-05 NBL-GWAS version 2 dbGaP|2895
NM_004565 PEX14 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs12741973 7.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_004566 PFKFB3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2185691 9.67E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_004571 PKNOX1 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Cholesterol rs2839619 8.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_004571 PKNOX1 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs2839627 6.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_004576 PPP2R2B 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs1864982 3.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_004576 PPP2R2B 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs9325032 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_004578 RAB4A 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs9287024 4.14E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_004578 RAB4A 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs41341649 1.61E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_004589 SCO1 19465909 http://www.ncbi.nlm.nih.gov/pubmed/19465909 Malaria rs6503319 7.00E-07 Genome-wide and fine-resolution association analysis of malaria in West Africa. NHGRI|-1
NM_004591 CCL20 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs7591163 3.00E-07 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_004593 TRA2B 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Attention Deficit Disorder with Hyperactivity rs10049246 8.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_004593 TRA2B 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs720390 2.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_004593 TRA2B 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs6444087 9.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_004593 TRA2B 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs2002675 1.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_004598 SPOCK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1229742 1.85E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_004598 SPOCK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2005698 1.71E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_004598 SPOCK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2673926 8.27E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_004598 SPOCK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2673925 7.34E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_004598 SPOCK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2673913 8.51E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_004604 STX4 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin rs10871454 5.00E-34 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_004613 TGM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6023059 6.26E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_004616 TSPAN8 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs1495377 7.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_004616 TSPAN8 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs4760790 4.00E-06 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_004616 TSPAN8 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7961581 1.00E-09 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_004616 TSPAN8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7980195 5.47E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_004619 TRAF5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3738200 4.83E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_004619 TRAF5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17189000 5.44E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_004622 TSN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4241112 9.25E-06 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_004622 TSN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17779391 3.76E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_004622 TSN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs11685781 1.31E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_004622 TSN 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs1527243 1.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_004622 TSN 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs17367118 9.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_004624 VIPR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs14380 1.21E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_004626 WNT11 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs4944092 3.00E-08 Genome-wide association study of PR interval. NHGRI|-1
NM_004631 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs5177 5.00E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_004631 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11206127 3.16E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_004631 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs869987 4.54E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_004631 LRP8 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs114216682 7.00E-08 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_004631 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17785382 1.74E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_004633 IL1R2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4851526 4.39E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_004633 IL1R2 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2310173 3.00E-12 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_004633 IL1R2 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs2310173 5.00E-07 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_004638 BAT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2242660 3.94E-109 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004638 BAT2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2242660 8.73E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_004638 BAT2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3115663 6.66E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_004638 BAT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1046089 1.28E-124 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004638 BAT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1046089 2.40E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_004638 BAT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1046089 1.30E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_004638 BAT2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1046089 3.79E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_004638 BAT2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs11229 5.55E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_004638 BAT2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2736177 3.15E-23 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_004639 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1077393 3.83E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_004639 BAT3 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs760293 9.72E-20 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_004639 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs805303 2.79E-119 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004639 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs805303 1.25E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_004639 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3130050 1.52E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004639 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3117583 3.33E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_004639 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3117582 2.62E-83 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004639 BAT3 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs3117582 4.00E-10 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_004639 BAT3 18978787 http://www.ncbi.nlm.nih.gov/pubmed/18978787 Lung Neoplasms rs3117582 5.00E-10 Common 5p15.33 and 6p21.33 variants influence lung cancer risk. NHGRI|-1
NM_004639 BAT3 19836008 http://www.ncbi.nlm.nih.gov/pubmed/19836008 Lung Neoplasms rs3117582 5.00E-12 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. NHGRI|-1
NM_004639 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3117582 4.53E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_004640 BAT1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3115537 2.46E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_004640 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3093978 8.82E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_004640 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3093948 8.72E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_004640 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3093976 1.03E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_004640 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3130057 1.07E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_004640 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2734583 5.29E-68 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_004640 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3130058 6.23E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_004640 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2516393 8.82E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_004640 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2239709 4.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_004640 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2251824 5.97E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_004647 DPF1 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs8102476 2.00E-11 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_004649 C21orf33 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2838519 6.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_004649 C21orf33 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs762421 1.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_004650 PNPLA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs5934349 1.75E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_004655 AXIN2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs757558 6.42E-06 NBL-GWAS version 1 dbGaP|2845
NM_004655 AXIN2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs8068707 2.40E-06 NBL-GWAS version 1 dbGaP|2845
NM_004658 RASAL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7976407 7.44E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_004667 HERC2 20463881 http://www.ncbi.nlm.nih.gov/pubmed/20463881 Eye Color rs12913832 1.00E-300 Digital quantification of human eye color highlights genetic association of three new loci. NHGRI|-1
NM_004667 HERC2 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs12913832 1.00E-300 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_004667 HERC2 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs12913832 3.00E-52 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_004667 HERC2 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs12913832 1.00E-77 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_004667 HERC2 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs12913832 4.00E-103 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_004667 HERC2 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12913832 9.00E-88 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_004667 HERC2 18252221 http://www.ncbi.nlm.nih.gov/pubmed/18252221 Eye Color rs916977 1.00E-43 Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene. NHGRI|-1
NM_004667 HERC2 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Eye Color rs1667394 1.00E-241 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_004667 HERC2 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Eye Color rs1667394 2.00E-53 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_004667 HERC2 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Hair Color rs1667394 6.00E-35 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_004670 PAPSS2 19727025 http://www.ncbi.nlm.nih.gov/pubmed/19727025 Exercise rs10887741 4.00E-06 Genome-wide association study of exercise behavior in Dutch and American adults. NHGRI|-1
NM_004685 MTMR6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs4769414 2.30E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_004685 MTMR6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4769414 9.34E-05 NBL-GWAS version 2 dbGaP|2895
NM_004689 MTA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9743822 1.35E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_004700 KCNQ4 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4660456 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_004704 RRP9 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs929533 3.79E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_004711 SYNGR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1569499 5.54E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_004711 SYNGR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4821888 1.14E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_004715 CTDP1 20801717 http://www.ncbi.nlm.nih.gov/pubmed/20801717 Amyotrophic Lateral Sclerosis rs4799088 9.00E-06 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. NHGRI|-1
NM_004715 CTDP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs537962 1.39E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_004715 CTDP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4799092 2.00E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_004716 PCSK7 21149283 http://www.ncbi.nlm.nih.gov/pubmed/21149283 Iron-Regulatory Proteins rs236918 1.00E-27 Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. NHGRI|-1
NM_004717 DGKI 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs6467710 6.00E-07 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_004717 DGKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2059320 9.58E-05 NBL-GWAS version 2 dbGaP|2895
NM_004721 MAP3K13 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs4687299 3.96E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_004728 DDX21 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs2017305 9.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_004731 SLC16A7 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs10506410 2.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_004734 DCLK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1539549 2.28E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_004734 DCLK1 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1926320 1.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_004734 DCLK1 17903306 http://www.ncbi.nlm.nih.gov/pubmed/17903306 Heart Rate rs9315385 8.00E-06 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. NHGRI|-1
NM_004737 LARGE 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs130575 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_004742 MAGI1 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6795735 2.00E-16 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_004742 MAGI1 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs4607103 1.00E-08 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_004742 MAGI1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10510933 3.46E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_004744 LRAT 18823527 http://www.ncbi.nlm.nih.gov/pubmed/18823527 Alzheimer Disease rs727153 3.00E-06 A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. NHGRI|-1
NM_004745 DLGAP2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4876063 8.39E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_004746 DLGAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs3915772 8.43E-05 NBL-GWAS version 2 dbGaP|2895
NM_004746 DLGAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs431220 5.88E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_004757 AIMP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4956263 6.74E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_004757 AIMP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4956263 7.90E-06 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_004767 GPR37L1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4436440 5.16E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_004767 GPR37L1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10800812 1.62E-08 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_004770 KCNB2 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 "Ventricular Function, Left" rs10504543 5.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_004770 KCNB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2587562 4.42E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_004770 KCNB2 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs1963982 3.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_004770 KCNB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1835482 2.58E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_004770 KCNB2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2116078 3.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_004772 C5orf13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs173896 5.04E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_004773 ZNHIT3 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Chemokine CCL4 rs4796217 4.00E-21 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_004775 B4GALT6 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs10438933 1.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_004784 NDST3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1489550 1.60E-06 NBL-GWAS version 1 dbGaP|2845
NM_004784 NDST3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs17862054 7.40E-06 NBL-GWAS version 1 dbGaP|2845
NM_004784 NDST3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1380376 8.04E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_004784 NDST3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1459544 9.24E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_004784 NDST3 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4422476 8.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_004786 TXNL1 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs1978503 1.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_004786 TXNL1 21160409 http://www.ncbi.nlm.nih.gov/pubmed/21160409 HIV-1 rs12604483 7.00E-06 Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population. NHGRI|-1
NM_004786 TXNL1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2538026 8.91E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_004786 TXNL1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs1229598 7.83E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_004787 SLIT2 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 "Ventricular Function, Left" rs666088 5.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_004787 SLIT2 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 "Ventricular Function, Left" rs1379659 1.00E-07 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_004796 NRXN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17107542 7.51E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_004796 NRXN3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs918270 5.55E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_004796 NRXN3 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10150332 3.00E-11 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_004796 NRXN3 19557197 http://www.ncbi.nlm.nih.gov/pubmed/19557197 Waist Circumference rs10146997 5.00E-08 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. NHGRI|-1
NM_004796 NRXN3 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs11624704 3.00E-09 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_004797 ADIPOQ 20018283 http://www.ncbi.nlm.nih.gov/pubmed/20018283 Adiponectin rs17366568 1.00E-41 Clear detection of ADIPOQ locus as the major gene for plasma adiponectin: results of genome-wide association analyses including 4659 European individuals. NHGRI|-1
NM_004797 ADIPOQ 19165155 http://www.ncbi.nlm.nih.gov/pubmed/19165155 Adiponectin rs6773957 5.00E-08 Genome-wide linkage and association analyses to identify genes influencing adiponectin levels: the GEMS Study. NHGRI|-1
NM_004797 ADIPOQ 20011104 http://www.ncbi.nlm.nih.gov/pubmed/20011104 Adiponectin rs266717 9.00E-19 A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. NHGRI|-1
NM_004797 ADIPOQ 20011104 http://www.ncbi.nlm.nih.gov/pubmed/20011104 Adiponectin rs1648707 3.00E-12 A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. NHGRI|-1
NM_004797 ADIPOQ 20876611 http://www.ncbi.nlm.nih.gov/pubmed/20876611 Adiponectin rs864265 1.00E-19 Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ. NHGRI|-1
NM_004800 TM9SF2 21700618 http://www.ncbi.nlm.nih.gov/pubmed/21700618 "Carcinoma, Basal Cell" rs7335046 3.00E-08 Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma. NHGRI|-1
NM_004801 NRXN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10196324 6.42E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_004801 NRXN1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs1356888 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_004801 NRXN1 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Exploratory Behavior rs10176705 9.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_004801 NRXN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs991902 3.48E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_004801 NRXN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2839839 7.09E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_004801 NRXN1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1156742 8.14E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_004815 ARHGAP29 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs2774920 1.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_004820 CYP7B1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs10808738 4.28E-06 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_004820 CYP7B1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7002672 5.04E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_004821 HAND1 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs13165478 7.00E-14 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_004821 HAND1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7731137 9.50E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_004822 NTN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7214739 4.94E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_004824 CDYL 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs73717741 3.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_004827 ABCG2 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs2231142 1.00E-10 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_004827 ABCG2 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs2231142 2.00E-18 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_004827 ABCG2 18834626 http://www.ncbi.nlm.nih.gov/pubmed/18834626 Uric Acid rs2231142 3.00E-60 Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study. NHGRI|-1
NM_004828 NCR2 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs9471576 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_004836 EIF2AK3 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs7571971 4.00E-13 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_004836 EIF2AK3 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs11684404 1.00E-13 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_004846 EIF4E2 21079520 http://www.ncbi.nlm.nih.gov/pubmed/21079520 "Carcinoma, Non-Small-Cell Lung" rs1656402 8.00E-08 Genome-wide association study on overall survival of advanced non-small cell lung cancer patients treated with carboplatin and paclitaxel. NHGRI|-1
NM_004849 ATG5 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs6568433 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_004849 ATG5 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Atrial Natriuretic Factor rs1417352 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_004849 ATG5 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs548234 5.00E-12 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_004850 ROCK2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs6716724 6.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_004853 STX8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4239104 4.79E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_004853 STX8 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs10521157 1.00E-08 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_004862 LITAF 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7203193 3.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_004862 LITAF 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs8049607 5.00E-15 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_004862 LITAF 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs8049607 6.00E-15 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_004867 ITM2A 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1474563 3.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_004893 H2AFY 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs31198 8.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_004893 H2AFY 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs254560 1.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_004893 H2AFY 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs477687 6.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_004895 NLRP3 20031576 http://www.ncbi.nlm.nih.gov/pubmed/20031576 Fibrinogen rs1539019 1.00E-08 Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. NHGRI|-1
NM_004895 NLRP3 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs12239046 1.00E-15 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_004895 NLRP3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10399826 2.06E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_004895 NLRP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11802371 1.11E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_004897 MINPP1 20304771 http://www.ncbi.nlm.nih.gov/pubmed/20304771 Longevity rs9664222 7.00E-07 A meta-analysis of four genome-wide association studies of survival to age 90 years or older: the Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium. NHGRI|-1
NM_004897 MINPP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12570629 9.12E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_004898 CLOCK 18957941 http://www.ncbi.nlm.nih.gov/pubmed/18957941 Personality rs6832769 2.00E-06 Genome-wide association scan for five major dimensions of personality. NHGRI|-1
NM_004899 BRE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs10189899 5.82E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_004904 CREB5 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs11765845 7.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_004904 CREB5 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2237349 5.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_004905 PRDX6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17350697 1.90E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_004906 WTAP 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs4516970 1.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_004915 ABCG1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Personality rs425215 8.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_004918 TCL1B 20876420 http://www.ncbi.nlm.nih.gov/pubmed/20876420 Aromatase Inhibitors rs7158782 8.00E-07 Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors. NHGRI|-1
NM_004926 ZFP36L1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs4902642 2.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_004926 ZFP36L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs4902642 8.54E-04 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_004930 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 2.00E-11 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_004930 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 3.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_004930 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12138950 3.00E-18 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_004930 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs10917468 1.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_004931 CD8B 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs6547705 1.00E-08 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_004934 CDH18 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs349475 2.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_004936 CDKN2B 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1063192 4.00E-15 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_004938 DAPK1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1923782 8.03E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_004938 DAPK1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4878061 2.42E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_004938 DAPK1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs1806864 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_004939 DDX1 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs7586898 2.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_004945 DNM2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11671653 9.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_004946 DOCK2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Leptin rs169082 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_004946 DOCK2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs259892 1.10E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_004946 DOCK2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs13361200 2.98E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_004958 MTOR 21665993 http://www.ncbi.nlm.nih.gov/pubmed/21665993 Corneal Topography rs17036350 4.00E-13 Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore. NHGRI|-1
NM_004967 IBSP 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs1054627 8.00E-07 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_004969 IDE 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs6583826 7.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_004969 IDE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11186960 8.74E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_004972 JAK2 19287384 http://www.ncbi.nlm.nih.gov/pubmed/19287384 Myeloproliferative Disorders rs10974944 4.00E-20 A germline JAK2 SNP is associated with predisposition to the development of JAK2(V617F)-positive myeloproliferative neoplasms. NHGRI|-1
NM_004972 JAK2 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs10758669 1.00E-06 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_004972 JAK2 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs10758669 2.00E-25 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_004972 JAK2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs10758669 3.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_004973 JARID2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11962776 3.94E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_004973 JARID2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs16876210 2.80E-05 NBL-GWAS version 2 dbGaP|2895
NM_004973 JARID2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7765425 5.07E-05 NBL-GWAS version 2 dbGaP|2895
NM_004974 KCNA2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7526730 2.14E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004974 KCNA2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6700661 4.20E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004974 KCNA2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs17025978 6.56E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_004974 KCNA2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7553815 3.96E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_004980 KCND3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11102457 1.72E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_004984 KIF5A 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 "Arthritis, Rheumatoid" rs1678542 9.00E-08 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_004985 KRAS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10505975 1.43E-05 NBL-GWAS version 2 dbGaP|2895
NM_004991 MECOM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs16852880 9.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_005007 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071593 4.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005007 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2523503 5.59E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005007 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2523500 2.64E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005007 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2255798 8.43E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005007 NFKBIL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2230365 2.52E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005010 NRCAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs409797 8.78E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_005012 ROR1 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs2749097 2.00E-09 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_005012 ROR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11208285 9.59E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_005012 ROR1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2819130 1.23E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_005020 PDE1C 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs215614 2.00E-07 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_005037 PPARG 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1801282 2.00E-06 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_005037 PPARG 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs1801282 2.00E-06 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_005037 PPARG 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs1801282 2.00E-06 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_005037 PPARG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs9833097 6.72E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_005038 PPID 20037589 http://www.ncbi.nlm.nih.gov/pubmed/20037589 Nonalcoholic Fatty Liver Disease rs8396 4.00E-24 A genome-wide perspective of genetic variation in human metabolism. NHGRI|-1
NM_005041 PRF1 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs10999409 5.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_005045 RELN 18282107 http://www.ncbi.nlm.nih.gov/pubmed/18282107 Schizophrenia rs7341475 9.00E-07 Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women. NHGRI|-1
NM_005045 RELN 19230858 http://www.ncbi.nlm.nih.gov/pubmed/19230858 Otosclerosis rs3914132 2.00E-08 A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis. NHGRI|-1
NM_005045 RELN 20452100 http://www.ncbi.nlm.nih.gov/pubmed/20452100 Neurofibrillary Tangles rs4298437 2.00E-06 Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study. NHGRI|-1
NM_005045 RELN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs17157903 1.03E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_005045 RELN 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs17157903 3.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_005066 SFPQ 21499250 http://www.ncbi.nlm.nih.gov/pubmed/21499250 Endometrial Neoplasms rs673604 6.00E-06 Genome-wide association study identifies a common variant associated with risk of endometrial cancer. NHGRI|-1
NM_005068 SIM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17060530 4.50E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_005068 SIM1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2841307 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_005074 SLC17A1 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs1165196 5.00E-25 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_005074 SLC17A1 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs17270561 5.00E-07 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_005074 SLC17A1 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs17342717 5.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_005074 SLC17A1 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs17342717 5.00E-09 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_005074 SLC17A1 21149283 http://www.ncbi.nlm.nih.gov/pubmed/21149283 Iron-Regulatory Proteins rs17342717 9.00E-10 Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. NHGRI|-1
NM_005074 SLC17A1 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs1183201 3.00E-14 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_005074 SLC17A1 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs1408272 1.00E-11 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_005074 SLC17A1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1408272 4.00E-39 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_005074 SLC17A1 21149283 http://www.ncbi.nlm.nih.gov/pubmed/21149283 Iron-Regulatory Proteins rs1408272 9.00E-09 Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. NHGRI|-1
NM_005078 TLE3 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs6494849 7.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_005084 PLA2G7 20442857 http://www.ncbi.nlm.nih.gov/pubmed/20442857 1-Alkyl-2-acetylglycerophosphocholine Esterase rs1805017 6.00E-14 Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study. NHGRI|-1
NM_005086 SSPN 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs718314 2.00E-17 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_005092 TNFSF18 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs859637 2.00E-06 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_005092 TNFSF18 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs9286879 2.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_005092 TNFSF18 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs12035082 2.00E-07 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_005095 ZMYM4 21499250 http://www.ncbi.nlm.nih.gov/pubmed/21499250 Endometrial Neoplasms rs673604 6.00E-06 Genome-wide association study identifies a common variant associated with risk of endometrial cancer. NHGRI|-1
NM_005098 MSC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4590481 1.09E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_005108 XYLB 19389651 http://www.ncbi.nlm.nih.gov/pubmed/19389651 Electrocardiography rs2070488 4.00E-06 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. NHGRI|-1
NM_005110 GFPT2 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs10464059 3.00E-06 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_005112 WDR1 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs717615 5.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_005114 HS3ST1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10516213 7.26E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_005116 SLC23A2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6107541 1.72E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_005116 SLC23A2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6116558 5.62E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_005116 SLC23A2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6107546 8.27E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_005118 TNFSF15 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs3810936 1.00E-15 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_005118 TNFSF15 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs4246905 6.00E-12 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_005118 TNFSF15 20018961 http://www.ncbi.nlm.nih.gov/pubmed/20018961 Leprosy rs6478108 3.00E-21 Genomewide association study of leprosy. NHGRI|-1
NM_005118 TNFSF15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs6478108 4.11E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_005118 TNFSF15 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs4263839 3.00E-10 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_005118 TNFSF15 18758464 http://www.ncbi.nlm.nih.gov/pubmed/18758464 Inflammatory Bowel Diseases rs6478109 3.00E-08 Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. NHGRI|-1
NM_005118 TNFSF15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs6478109 9.12E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_005118 TNFSF15 21699788 http://www.ncbi.nlm.nih.gov/pubmed/21699788 Inflammatory Bowel Diseases rs2006996 4.00E-13 HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease. NHGRI|-1
NM_005118 TNFSF15 21699788 http://www.ncbi.nlm.nih.gov/pubmed/21699788 Inflammatory Bowel Diseases rs2006996 4.00E-16 HLA-Cw*1202-B*5201-DRB1*1502 Haplotype Increases Risk for Ulcerative Colitis But Reduces Risk for Crohn's Disease. NHGRI|-1
NM_005118 TNFSF15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs7866342 1.01E-05 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_005118 TNFSF15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs10114470 4.08E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_005124 NUP153 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs9350051 3.08E-06 NBL-GWAS version 1 dbGaP|2845
NM_005124 NUP153 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs6929659 7.09E-07 NBL-GWAS version 1 dbGaP|2845
NM_005124 NUP153 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs12199222 7.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_005131 THOC1 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs7226677 4.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_005131 THOC1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs7226677 7.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_005141 FGB 20031576 http://www.ncbi.nlm.nih.gov/pubmed/20031576 Fibrinogen rs1800789 2.00E-30 Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. NHGRI|-1
NM_005141 FGB 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs6056 8.00E-39 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_005155 PPT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3134603 3.36E-116 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005155 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3096697 2.16E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_005155 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3096697 5.66E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_005155 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130347 1.22E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_005155 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130347 3.62E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_005157 ABL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1046129 9.47E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_005170 ASCL2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs7111341 4.00E-48 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_005170 ASCL2 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs7127900 3.00E-33 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_005171 ATF1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs17291650 3.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_005171 ATF1 20972440 http://www.ncbi.nlm.nih.gov/pubmed/20972440 Colorectal Neoplasms rs11169552 2.00E-10 "Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33." NHGRI|-1
NM_005176 ATP5G2 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs11170631 9.00E-07 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_005184 CALM2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs815815 7.00E-07 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_005189 CBX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs3751954 9.51E-06 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_005192 CDKN3 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs4293296 3.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_005194 CEBPB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs913678 3.19E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005194 CEBPB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4811072 6.50E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_005198 CHKB 18820697 http://www.ncbi.nlm.nih.gov/pubmed/18820697 Narcolepsy rs5770917 6.00E-08 Variant between CPT1B and CHKB associated with susceptibility to narcolepsy. NHGRI|-1
NM_005204 MAP3K8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs3124177 2.70E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_005204 MAP3K8 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10763807 1.45E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_005213 CSTA 20558539 http://www.ncbi.nlm.nih.gov/pubmed/20558539 Phosphorus rs17265703 4.00E-09 Common genetic variants associate with serum phosphorus concentration. NHGRI|-1
NM_005214 CTLA4 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs3087243 1.00E-08 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_005214 CTLA4 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs3087243 1.00E-15 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_005214 CTLA4 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs3087243 8.00E-11 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_005214 CTLA4 19503088 http://www.ncbi.nlm.nih.gov/pubmed/19503088 "Arthritis, Rheumatoid" rs231735 6.00E-09 "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis." NHGRI|-1
NM_005214 CTLA4 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs1024161 4.00E-13 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_005215 DCC 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs768048 8.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_005215 DCC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs965943 8.37E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_005215 DCC 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs4401133 3.70E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_005216 DDOST 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs640742 2.90E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_005224 ARID3A 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs2159128 3.00E-07 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_005228 EGFR 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs11979158 7.00E-08 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_005228 EGFR 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs2252586 8.00E-08 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_005230 ELK3 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs2660869 3.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_005232 EPHA1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs11767557 6.00E-10 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_005233 EPHA3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs9832305 6.12E-06 NBL-GWAS version 1 dbGaP|2845
NM_005233 EPHA3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs6782527 9.75E-07 NBL-GWAS version 1 dbGaP|2845
NM_005233 EPHA3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs6774870 3.32E-06 NBL-GWAS version 1 dbGaP|2845
NM_005233 EPHA3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs907548 5.53E-06 NBL-GWAS version 1 dbGaP|2845
NM_005233 EPHA3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1915304 3.23E-06 NBL-GWAS version 1 dbGaP|2845
NM_005233 EPHA3 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs2880961 2.00E-07 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_005235 ERBB4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1851196 5.11E-06 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_005235 ERBB4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs839511 2.58E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_005235 ERBB4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs16849204 3.22E-05 NBL-GWAS version 2 dbGaP|2895
NM_005235 ERBB4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7600221 6.53E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_005235 ERBB4 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Eosinophils rs12619285 5.00E-10 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_005236 ERCC4 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs3136202 6.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_005236 ERCC4 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs10521095 2.34E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_005236 ERCC4 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs2113334 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_005238 ETS1 20169177 http://www.ncbi.nlm.nih.gov/pubmed/20169177 "Lupus Erythematosus, Systemic" rs1128334 2.00E-11 Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus. NHGRI|-1
NM_005238 ETS1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs11221332 5.00E-16 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_005238 ETS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs11221064 1.60E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_005238 ETS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7130878 1.66E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_005238 ETS1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs6590322 9.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_005238 ETS1 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs6590330 2.00E-25 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_005239 ETS2 21079520 http://www.ncbi.nlm.nih.gov/pubmed/21079520 "Carcinoma, Non-Small-Cell Lung" rs1209950 3.00E-07 Genome-wide association study on overall survival of advanced non-small cell lung cancer patients treated with carboplatin and paclitaxel. NHGRI|-1
NM_005241 MECOM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs16852880 9.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_005245 FAT1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs925642 7.00E-06 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_005250 FOXL1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs10048146 2.00E-07 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_005250 FOXL1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs10048146 2.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_005253 FOSL2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2940787 1.92E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_005255 GAK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1564282 5.99E-06 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_005255 GAK 18985386 http://www.ncbi.nlm.nih.gov/pubmed/18985386 Parkinson Disease rs1564282 7.00E-07 Genomewide association study for susceptibility genes contributing to familial Parkinson disease. NHGRI|-1
NM_005255 GAK 20711177 http://www.ncbi.nlm.nih.gov/pubmed/20711177 Parkinson Disease rs11248051 3.00E-09 Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. NHGRI|-1
NM_005255 GAK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11248051 5.25E-06 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_005256 GAS2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs7111546 2.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_005257 GATA6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4800370 8.92E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_005257 GATA6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11664999 9.70E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_005257 GATA6 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs9950004 5.29E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_005265 GGT1 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs4820599 4.00E-11 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_005265 GGT1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 gamma-Glutamyltransferase rs5751901 2.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_005267 GJA8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2132397 1.28E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_005268 GJB5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs10914952 1.64E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_005268 GJB5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2359631 6.37E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_005268 GJB5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs612353 9.05E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_005270 GLI2 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs11122834 5.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_005270 GLI2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs12467309 2.59E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_005270 GLI2 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs7581710 2.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_005275 GNL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs10484552 7.49E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_005277 GPM6A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1495714 1.93E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005277 GPM6A 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs7687921 4.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_005277 GPM6A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4690647 1.13E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005283 XCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10510749 4.22E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005283 XCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7631551 7.95E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005283 XCR1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs13098911 3.00E-17 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_005285 NPBWR1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs360968 1.32E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_005285 NPBWR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1426562 3.34E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_005285 NPBWR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs6473783 5.28E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_005288 GPR12 19187332 http://www.ncbi.nlm.nih.gov/pubmed/19187332 Asthma rs9319321 3.00E-06 Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis. NHGRI|-1
NM_005288 GPR12 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs17084857 7.67E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_005288 GPR12 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs17085007 1.00E-16 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_005288 GPR12 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 "Colitis, Ulcerative" rs17085007 7.00E-08 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_005293 GPR20 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7839244 6.76E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_005293 GPR20 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs7386474 3.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_005301 GPR35 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs4676406 8.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_005308 GRK5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10886492 7.15E-05 NBL-GWAS version 2 dbGaP|2895
NM_005308 GRK5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2991769 3.09E-05 NBL-GWAS version 2 dbGaP|2895
NM_005308 GRK5 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2991769 7.72E-07 NBL-GWAS version 1 dbGaP|2845
NM_005308 GRK5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2991770 1.76E-05 NBL-GWAS version 2 dbGaP|2895
NM_005308 GRK5 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2991770 8.71E-07 NBL-GWAS version 1 dbGaP|2845
NM_005314 GRPR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs798159 4.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_005320 HIST1H1D 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs10946808 4.00E-17 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_005320 HIST1H1D 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10946808 6.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_005320 HIST1H1D 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs10946808 6.00E-12 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_005322 HIST1H1B 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs200953 3.82E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_005323 HIST1H1T 19820698 http://www.ncbi.nlm.nih.gov/pubmed/19820698 Hemoglobins rs198846 1.00E-08 Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels. NHGRI|-1
NM_005323 HIST1H1T 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs12206204 8.00E-07 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_005328 HAS2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs17232789 6.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_005329 HAS3 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs8047014 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_005330 HBE1 18245381 http://www.ncbi.nlm.nih.gov/pubmed/18245381 Fetal Hemoglobin rs4910742 1.00E-21 Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. NHGRI|-1
NM_005333 HCCS 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs5934953 1.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_005338 HIP1 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs1167796 2.00E-08 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_005338 HIP1 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs237238 7.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_005345 HSPA1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2763979 3.26E-99 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005345 HSPA1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2763979 8.14E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_005346 HSPA1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2763979 3.26E-99 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005346 HSPA1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2763979 8.14E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_005349 RBPJ 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs10517086 5.00E-10 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_005349 RBPJ 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs874040 1.00E-16 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_005359 SMAD4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9807334 6.28E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_005360 MAF 19151714 http://www.ncbi.nlm.nih.gov/pubmed/19151714 Obesity rs1424233 4.00E-13 Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. NHGRI|-1
NM_005360 MAF 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs17767419 9.00E-15 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_005360 MAF 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs3813579 4.00E-10 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_005360 MAF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1396702 6.06E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_005360 MAF 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4888984 4.71E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_005360 MAF 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4888984 9.48E-06 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_005360 MAF 20668459 http://www.ncbi.nlm.nih.gov/pubmed/20668459 Body Height rs7498403 5.00E-06 Genetic variants that affect length/height in infancy/early childhood in Vietnamese-Korean families. NHGRI|-1
NM_005371 METTL1 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs703842 5.00E-11 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_005375 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs7775698 1.00E-14 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_005375 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs7775698 1.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_005375 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-56 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_005375 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-66 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_005375 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 5.00E-13 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_005375 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 8.00E-18 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_005375 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7776054 7.00E-69 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_005375 MYB 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs9399137 3.00E-36 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_005375 MYB 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Platelet Count rs9399137 1.00E-09 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_005375 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9373124 7.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_005375 MYB 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs9373124 1.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_005375 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4895441 7.00E-86 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_005375 MYB 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs4895441 2.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_005375 MYB 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs9376092 2.00E-11 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_005375 MYB 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9402686 7.00E-42 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_005375 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs9494145 3.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_005375 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Count rs9483788 1.00E-47 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_005375 MYB 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs9483788 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_005375 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 1.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_005375 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 3.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_005375 MYB 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 6.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_005382 NEFM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1457266 4.27E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_005384 NFIL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1591068 8.21E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_005384 NFIL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1855065 4.28E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_005390 PDHA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2204919 7.80E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_005398 PPP1R3C 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs1329650 6.00E-10 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_005400 PRKCE 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Count rs10495928 4.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_005400 PRKCE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs10495928 7.00E-13 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_005400 PRKCE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs10168349 4.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_005400 PRKCE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12622230 4.02E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_005401 PTPN14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs6657749 4.68E-06 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_005419 STAT2 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs2066808 1.00E-09 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NM_005419 STAT2 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs2066808 2.00E-07 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_005419 STAT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11575221 5.71E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_005425 TNP2 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs416603 3.00E-06 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_005441 CHAF1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs218626 4.70E-05 NBL-GWAS version 2 dbGaP|2895
NM_005442 EOMES 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs12632457 1.90E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_005450 NOG 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs227731 1.00E-08 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_005450 NOG 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs4794665 1.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_005458 GABBR2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs12351127 4.09E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_005458 GABBR2 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs1167768 7.34E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_005461 MAFB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs3092685 1.39E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_005461 MAFB 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2224536 3.95E-07 NBL-GWAS version 1 dbGaP|2845
NM_005461 MAFB 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 "Arthritis, Rheumatoid" rs6028945 2.00E-07 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_005461 MAFB 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs6102059 4.00E-09 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_005465 AKT3 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs4132509 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_005465 AKT3 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs10927101 2.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_005465 AKT3 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs476141 1.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_005465 AKT3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1000543 1.25E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_005465 AKT3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2454222 6.14E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_005465 AKT3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2454221 8.28E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_005465 AKT3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2047137 9.15E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_005467 NAALAD2 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs11018874 2.00E-09 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_005471 GNPDA1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs409037 4.58E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_005474 HDAC5 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs228769 2.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_005474 HDAC5 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs228769 4.00E-06 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_005475 SH2B3 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs3184504 6.00E-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_005475 SH2B3 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs3184504 3.00E-14 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_005475 SH2B3 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs3184504 5.00E-09 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_005475 SH2B3 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs3184504 6.00E-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_005475 SH2B3 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs3184504 3.00E-27 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_005475 SH2B3 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Eosinophils rs3184504 7.00E-19 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_005485 PARP3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs929533 3.79E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_005486 TOM1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7207449 1.46E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_005494 DNAJB6 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs10227331 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_005494 DNAJB6 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Blood Pressure rs2527866 3.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_005502 ABCA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs3818688 2.61E-04 Genome-wide association between genotype and incident myocardial infarction in African-American participants dbGaP|2883
NM_005502 ABCA1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs2515629 5.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_005502 ABCA1 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs4149268 1.00E-10 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_005502 ABCA1 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, HDL" rs3890182 3.00E-10 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_005502 ABCA1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs3890182 5.00E-07 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_005502 ABCA1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs3905000 9.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_005502 ABCA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Blood Pressure rs3905000 9.10E-05 Genomewide association analysis of diastolic blood pressure (DBP) in a birth cohort from a founder population dbGaP|2898
NM_005502 ABCA1 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, HDL" rs3905000 9.00E-13 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_005502 ABCA1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs1883025 1.00E-09 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_005504 BCAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10505955 4.33E-04 Genome-wide association between genotype and incident stroke in participants of primarily self-described European ancestry dbGaP|2886
NM_005505 SCARB1 21729881 http://www.ncbi.nlm.nih.gov/pubmed/21729881 Vitamin E rs11057830 8.00E-09 Genome-wide association study identifies common variants associated with circulating vitamin E levels NHGRI|-1
NM_005505 SCARB1 20442857 http://www.ncbi.nlm.nih.gov/pubmed/20442857 1-Alkyl-2-acetylglycerophosphocholine Esterase rs10846744 1.00E-08 Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study. NHGRI|-1
NM_005505 SCARB1 21131975 http://www.ncbi.nlm.nih.gov/pubmed/21131975 "Carcinoma, Renal Cell" rs4765623 3.00E-08 Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3. NHGRI|-1
NM_005505 SCARB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7956328 6.36E-06 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_005505 SCARB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7956328 8.55E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_005506 SCARB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6532244 2.09E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_005508 CCR4 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs13314993 3.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_005508 CCR4 21105107 http://www.ncbi.nlm.nih.gov/pubmed/21105107 "Carcinoma, Hepatocellular" rs4678680 2.00E-07 Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma. NHGRI|-1
NM_005510 DOM3Z 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs416002 9.33E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_005510 DOM3Z 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs389884 8.47E-87 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005510 DOM3Z 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs389884 2.08E-18 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_005510 DOM3Z 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs389884 9.42E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_005510 DOM3Z 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs387608 1.91E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_005510 DOM3Z 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs387608 6.95E-09 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_005512 LRRC32 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3740778 7.68E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_005512 LRRC32 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2155219 5.00E-16 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_005512 LRRC32 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs7927894 1.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_005512 LRRC32 19349984 http://www.ncbi.nlm.nih.gov/pubmed/19349984 "Dermatitis, Atopic" rs7927894 8.00E-10 A common variant on chromosome 11q13 is associated with atopic dermatitis. NHGRI|-1
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs78586586 1.31E-27 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112985979 3.41E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005514 HLA-B 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs2523608 3.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_005514 HLA-B 21051598 http://www.ncbi.nlm.nih.gov/pubmed/21051598 HIV-1 rs2523608 9.00E-20 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. NHGRI|-1
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113905114 4.34E-09 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2523591 4.54E-14 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005514 HLA-B 21051598 http://www.ncbi.nlm.nih.gov/pubmed/21051598 HIV-1 rs2523590 2.00E-13 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. NHGRI|-1
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111887764 3.43E-13 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113026024 1.91E-45 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs28367594 7.32E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005514 HLA-B 20526339 http://www.ncbi.nlm.nih.gov/pubmed/20526339 Vitiligo rs9468925 2.00E-33 Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. NHGRI|-1
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs1819788 3.16E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2524163 5.33E-20 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2243868 9.44E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2243868 2.80E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_005514 HLA-B 20512145 http://www.ncbi.nlm.nih.gov/pubmed/20512145 Nasopharyngeal Neoplasms rs2894207 3.00E-33 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. NHGRI|-1
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2894207 3.77E-38 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9380237 2.58E-28 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2524132 1.95E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9468933 1.62E-46 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2853924 2.31E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_005514 HLA-B 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2247056 5.16E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113608210 4.16E-13 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2853923 2.70E-15 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_005514 HLA-B 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2524095 5.57E-08 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs16899202 5.26E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112968141 3.22E-10 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005514 HLA-B 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2524089 2.05E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9380240 4.41E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111310861 2.85E-10 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9468937 4.83E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9264868 1.18E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9264869 1.95E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9264870 1.95E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_005514 HLA-B 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Interleukin-18 rs9461688 4.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9264885 6.30E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3873386 1.00E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3873386 1.17E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_005514 HLA-B 21051598 http://www.ncbi.nlm.nih.gov/pubmed/21051598 HIV-1 rs9264942 3.00E-35 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. NHGRI|-1
NM_005514 HLA-B 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs9264942 6.00E-12 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_005514 HLA-B 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs9264942 6.00E-32 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_005514 HLA-B 19115949 http://www.ncbi.nlm.nih.gov/pubmed/19115949 Acquired Immunodeficiency Syndrome rs10484554 6.00E-08 Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). NHGRI|-1
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111540800 8.12E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005514 HLA-B 18369459 http://www.ncbi.nlm.nih.gov/pubmed/18369459 Psoriasis rs10484554 2.00E-39 A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. NHGRI|-1
NM_005514 HLA-B 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs10484554 4.00E-214 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_005514 HLA-B 18364390 http://www.ncbi.nlm.nih.gov/pubmed/18364390 Psoriasis rs3134792 1.00E-09 Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene. NHGRI|-1
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2156875 3.71E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_005514 HLA-B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2442719 2.81E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_005515 MNX1 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs6966038 4.00E-07 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_005515 MNX1 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs6966038 5.00E-07 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_005516 HLA-E 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264459 4.51E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005516 HLA-E 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs10484552 7.49E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_005527 HSPA1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2227956 1.23E-115 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005531 IFI16 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs1772408 8.00E-07 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_005538 INHBC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs776037 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_005538 INHBC 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs1106766 2.00E-11 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_005541 INPP5D 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs10933436 7.00E-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_005544 IRS1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7578326 5.00E-20 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_005544 IRS1 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs2943634 2.00E-07 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_005544 IRS1 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs2943641 9.00E-12 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_005544 IRS1 21706003 http://www.ncbi.nlm.nih.gov/pubmed/21706003 Adiposity rs2943650 4.00E-11 Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile. NHGRI|-1
NM_005544 IRS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs964818 4.37E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_005544 IRS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4510219 4.86E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_005544 IRS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3914465 1.85E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_005544 IRS1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs13032261 4.49E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_005544 IRS1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4129068 2.87E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_005544 IRS1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4129068 5.82E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_005544 IRS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs11903929 4.37E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_005546 ITK 21368711 http://www.ncbi.nlm.nih.gov/pubmed/21368711 Personality rs411174 1.00E-06 Genome-wide association study of personality traits in bipolar patients. NHGRI|-1
NM_005549 KCNA10 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7526730 2.14E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_005549 KCNA10 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6700661 4.20E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_005549 KCNA10 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs17025978 6.56E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_005549 KCNA10 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7553815 3.96E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_005549 KCNA10 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7543509 4.37E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_005549 KCNA10 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7543509 8.48E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_005551 KLK2 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs2735839 2.00E-18 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_005559 LAMA1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7227276 6.48E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_005559 LAMA1 20876614 http://www.ncbi.nlm.nih.gov/pubmed/20876614 "Carcinoma, Non-Small-Cell Lung" rs16951095 7.00E-06 A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population. NHGRI|-1
NM_005559 LAMA1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs597503 2.00E-08 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_005560 LAMA5 20972440 http://www.ncbi.nlm.nih.gov/pubmed/20972440 Colorectal Neoplasms rs4925386 2.00E-10 "Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33." NHGRI|-1
NM_005561 LAMP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12871648 4.98E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_005562 LAMC2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs1028771 4.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_005562 LAMC2 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs525410 6.00E-07 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_005566 LDHA 21124955 http://www.ncbi.nlm.nih.gov/pubmed/21124955 Serum Amyloid A Protein rs2896526 4.00E-22 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. NHGRI|-1
NM_005569 LIMK2 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic Nephropathies rs2106294 4.00E-06 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_005574 LMO2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4756052 3.29E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_005576 LOXL1 17690259 http://www.ncbi.nlm.nih.gov/pubmed/17690259 Exfoliation Syndrome rs3825942 3.00E-21 Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma. NHGRI|-1
NM_005576 LOXL1 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs893817 3.00E-06 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_005577 LPA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6919346 4.74E-12 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_005577 LPA 19124843 http://www.ncbi.nlm.nih.gov/pubmed/19124843 Lipoprotein(a) rs6919346 4.00E-11 Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q. NHGRI|-1
NM_005577 LPA 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs3798220 3.00E-11 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_005577 LPA 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Lipoprotein(a) rs7770628 4.00E-10 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_005578 LPP 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1464510 3.00E-40 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_005578 LPP 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs1464510 5.00E-09 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_005578 LPP 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs1464510 1.00E-11 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_005578 LPP 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Mass Index rs1152846 3.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_005578 LPP 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs1152846 6.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_005586 MDFI 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2842643 3.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_005589 ALDH6A1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Circadian Rhythm rs2239557 3.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_005595 NFIA 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs6691768 1.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_005595 NFIA 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9436640 5.00E-18 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_005595 NFIA 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs2989476 3.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_005595 NFIA 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs472913 2.00E-07 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_005596 NFIB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10435726 4.14E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_005596 NFIB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10435726 6.42E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_005597 NFIC 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs7507204 4.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_005597 NFIC 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs11669592 4.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_005602 CLDN11 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs6444931 6.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_005602 CLDN11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6444931 1.96E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_005603 ATP8B1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1893673 7.75E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_005604 POU3F2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Thyrotropin rs6909430 8.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_005604 POU3F2 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs9491640 9.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_005605 PPP3CC 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs4872511 9.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_005605 PPP3CC 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs2280890 9.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_005611 RBL2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12444248 3.90E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_005612 REST 21106707 http://www.ncbi.nlm.nih.gov/pubmed/21106707 Bleomycin rs708547 9.00E-07 A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity. NHGRI|-1
NM_005613 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2343331 2.46E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_005613 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2343278 9.28E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_005613 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2841974 4.67E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_005613 RGS4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2841979 9.97E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_005620 S100A11 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs3124314 4.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_005628 SLC1A5 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs11668878 4.00E-07 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_005634 SOX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12834774 3.38E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_005637 SS18 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs1840440 3.00E-07 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_005646 TARBP1 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs10489896 6.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_005646 TARBP1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs744487 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_005647 TBL1X 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1024443 6.38E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_005657 TP53BP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2439832 9.27E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_005658 TRAF1 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs3761847 2.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_005658 TRAF1 17804836 http://www.ncbi.nlm.nih.gov/pubmed/17804836 "Arthritis, Rheumatoid" rs3761847 4.00E-14 TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. NHGRI|-1
NM_005658 TRAF1 19503088 http://www.ncbi.nlm.nih.gov/pubmed/19503088 "Arthritis, Rheumatoid" rs881375 4.00E-08 "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis." NHGRI|-1
NM_005666 CFHR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3790414 2.51E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_005666 CFHR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3790414 6.21E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_005666 CFHR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7531555 4.87E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_005666 CFHR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6667243 1.13E-57 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_005666 CFHR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6667243 3.34E-66 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_005666 CFHR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7548070 2.60E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_005666 CFHR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7548070 4.93E-21 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_005666 CFHR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4915318 5.49E-30 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_005666 CFHR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4915318 5.91E-34 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_005666 CFHR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7538501 2.02E-20 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_005666 CFHR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7538501 7.55E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_005668 ST8SIA4 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs13188771 2.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_005668 ST8SIA4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs6885006 9.61E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_005668 ST8SIA4 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs4702982 6.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_005669 REEP5 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs469727 8.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_005672 PSCA 19648920 http://www.ncbi.nlm.nih.gov/pubmed/19648920 Urinary Bladder Neoplasms rs2294008 2.00E-10 Genetic variation in the prostate stem cell antigen gene PSCA confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_005672 PSCA 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs2294008 4.00E-11 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_005677 COLQ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12495710 4.38E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_005691 ABCC9 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs10743430 6.00E-07 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_005693 NR1H3 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, HDL" rs7120118 4.00E-08 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_005693 NR1H3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs7120118 3.57E-08 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_005697 SCAMP2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8025170 1.54E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_005697 SCAMP2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8029351 1.54E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_005698 SCAMP3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs1142287 2.00E-13 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_005704 PTPRU 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1932397 7.14E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_005704 PTPRU 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9286938 9.14E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_005704 PTPRU 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs4949526 4.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_005704 PTPRU 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11580589 2.48E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_005704 PTPRU 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs910696 3.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_005704 PTPRU 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs2180233 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_005708 GPC6 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs1116260 2.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_005708 GPC6 20634892 http://www.ncbi.nlm.nih.gov/pubmed/20634892 Neurotic Disorders rs9561329 1.00E-07 A genome-wide association study of neuroticism in a population-based sample. NHGRI|-1
NM_005708 GPC6 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs7995215 1.00E-08 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_005711 EDIL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4703978 3.22E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_005711 EDIL3 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs347344 1.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NM_005711 EDIL3 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs7717527 2.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_005711 EDIL3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10052280 1.04E-04 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_005711 EDIL3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1552984 7.81E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_005711 EDIL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4920821 9.66E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_005711 EDIL3 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 "Ventricular Function, Left" rs4920799 7.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_005715 UST 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs2500535 4.00E-08 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_005715 UST 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs2500535 9.00E-06 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_005715 UST 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs7772697 3.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_005715 UST 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Count rs636864 6.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_005715 UST 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Count rs727979 8.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_005725 TSPAN2 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs195204 9.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_005729 PPIF 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2145998 4.00E-13 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_005732 RAD50 20159242 http://www.ncbi.nlm.nih.gov/pubmed/20159242 Asthma rs2244012 3.00E-07 Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. NHGRI|-1
NM_005732 RAD50 18846228 http://www.ncbi.nlm.nih.gov/pubmed/18846228 Immunoglobulin E rs2040704 4.00E-08 Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus. NHGRI|-1
NM_005737 ARL4C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10167927 8.69E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_005737 ARL4C 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs6736997 6.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_005737 ARL4C 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs2042831 7.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_005738 ARL4A 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs732577 4.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_005739 RASGRP1 18840781 http://www.ncbi.nlm.nih.gov/pubmed/18840781 "Diabetes Mellitus, Type 1" rs8035957 4.00E-06 Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes. NHGRI|-1
NM_005739 RASGRP1 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs12912251 1.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_005756 GPR64 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs5955711 9.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_005759 ABI2 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 "Carotid Artery, Internal" rs1376877 4.00E-07 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_005761 PLXNC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs865569 8.93E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_005765 ATP6AP2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs12008633 4.51E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_005766 FARP1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs4318070 7.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_005766 FARP1 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs688872 1.00E-06 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_005766 FARP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs688872 4.44E-04 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_005766 FARP1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs9584805 2.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_005772 RCL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7860776 6.95E-06 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_005772 RCL1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs10758658 2.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_005772 RCL1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs10758658 3.00E-20 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_005772 RCL1 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs10758669 1.00E-06 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_005772 RCL1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs10758669 2.00E-25 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_005772 RCL1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs10758669 3.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_005775 SORBS3 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs4872511 9.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_005775 SORBS3 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs2280890 9.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_005777 RBM6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2681779 6.15E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_005777 RBM6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2624821 6.07E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_005777 RBM6 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs6762477 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_005778 RBM5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2624834 4.44E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_005788 PRMT3 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs7128311 5.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_005792 MPHOSPH6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2967391 1.52E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_005792 MPHOSPH6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2967340 2.14E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_005792 MPHOSPH6 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Bone Density rs4087296 3.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_005792 MPHOSPH6 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs4082514 3.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_005792 MPHOSPH6 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs1991867 4.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_005792 MPHOSPH6 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Benzodiazepines rs4783227 4.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_005792 MPHOSPH6 19304780 http://www.ncbi.nlm.nih.gov/pubmed/19304780 Hypertension rs11646213 8.00E-06 Genome-wide scan identifies CDH13 as a novel susceptibility locus contributing to blood pressure determination in two European populations. NHGRI|-1
NM_005792 MPHOSPH6 20887962 http://www.ncbi.nlm.nih.gov/pubmed/20887962 Adiponectin rs3865188 3.00E-83 Adiponectin concentrations: a genome-wide association study. NHGRI|-1
NM_005792 MPHOSPH6 20876611 http://www.ncbi.nlm.nih.gov/pubmed/20876611 Adiponectin rs3865188 4.00E-30 Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ. NHGRI|-1
NM_005795 CALCRL 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs840616 7.00E-07 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_005796 NUTF2 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, HDL" rs2271293 8.00E-16 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_005796 NUTF2 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs2271293 9.00E-13 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_005796 NUTF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs2271293 4.66E-08 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_005797 MPZL2 19207018 http://www.ncbi.nlm.nih.gov/pubmed/19207018 Pain Measurement rs17122021 7.00E-07 Genome-wide association study of acute post-surgical pain in humans. NHGRI|-1
NM_005800 USPL1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs11618202 7.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_005803 FLOT1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs3094127 1.30E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_005803 FLOT1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs3095329 3.00E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_005808 CTDSPL 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Prostatic Neoplasms rs9311171 2.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_005813 PRKD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1158219 3.60E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_005816 CD96 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs76884941 1.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_005816 CD96 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs56238310 1.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_005819 STX6 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs1411478 4.00E-11 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_005831 CALCOCO2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs563916 4.11E-06 NBL-GWAS version 2 dbGaP|2895
NM_005832 KCNMB2 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs9290663 6.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_005832 KCNMB2 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs12629106 4.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_005832 KCNMB2 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs644695 5.00E-06 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_005832 KCNMB2 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs7612209 4.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_005832 KCNMB2 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs1982821 4.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_005842 SPRY2 21706003 http://www.ncbi.nlm.nih.gov/pubmed/21706003 Adiposity rs534870 7.00E-08 Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile. NHGRI|-1
NM_005842 SPRY2 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs2039553 7.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_005842 SPRY2 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs9574565 3.00E-07 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_005842 SPRY2 20862305 http://www.ncbi.nlm.nih.gov/pubmed/20862305 "Diabetes Mellitus, Type 2" rs1359790 6.00E-09 Identification of new genetic risk variants for type 2 diabetes. NHGRI|-1
NM_005845 ABCC4 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4148546 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_005845 ABCC4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1189428 2.40E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_005845 ABCC4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4148490 2.10E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_005845 ABCC4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4148475 4.40E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_005845 ABCC4 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs1926657 2.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_005845 ABCC4 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs9302001 3.00E-07 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_005848 DENND4A 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs6494537 3.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_005850 SF3B4 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs11205277 1.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_005853 IRX5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs17210989 1.49E-05 NBL-GWAS version 2 dbGaP|2895
NM_005853 IRX5 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs17291845 5.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_005865 PRSS16 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs6932590 1.00E-12 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_005867 DSCR4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2836079 8.86E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_005900 SMAD1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs568752 1.70E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_005902 SMAD3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs17293632 3.00E-19 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_005902 SMAD3 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs744910 4.00E-09 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_005902 SMAD3 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs17228212 2.00E-07 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_005904 SMAD7 17934461 http://www.ncbi.nlm.nih.gov/pubmed/17934461 Colorectal Neoplasms rs4939827 1.00E-12 A genome-wide association study shows that common alleles of SMAD7 influence colorectal cancer risk. NHGRI|-1
NM_005904 SMAD7 18372905 http://www.ncbi.nlm.nih.gov/pubmed/18372905 Colorectal Neoplasms rs4939827 2.00E-06 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. NHGRI|-1
NM_005904 SMAD7 18372901 http://www.ncbi.nlm.nih.gov/pubmed/18372901 Colorectal Neoplasms rs4939827 8.00E-28 Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. NHGRI|-1
NM_005908 MANBA 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs7665090 4.00E-12 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_005909 MAP1B 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2199161 2.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_005910 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17563986 3.44E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_005910 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs242557 9.00E-18 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_005910 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1981997 2.02E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_005910 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs8070723 3.36E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_005910 MAPT 21044948 http://www.ncbi.nlm.nih.gov/pubmed/21044948 Parkinson Disease rs8070723 7.00E-12 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. NHGRI|-1
NM_005910 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs8070723 2.00E-118 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_005912 MC4R 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs11878133 4.00E-06 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_005912 MC4R 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs4257308 6.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_005912 MC4R 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs571312 6.00E-42 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_005912 MC4R 18454148 http://www.ncbi.nlm.nih.gov/pubmed/18454148 Body Mass Index rs17782313 3.00E-15 "Common variants near MC4R are associated with fat mass, weight and risk of obesity." NHGRI|-1
NM_005912 MC4R 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs17782313 5.00E-18 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_005912 MC4R 19151714 http://www.ncbi.nlm.nih.gov/pubmed/19151714 Obesity rs17782313 5.00E-15 Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. NHGRI|-1
NM_005912 MC4R 20421936 http://www.ncbi.nlm.nih.gov/pubmed/20421936 Obesity rs10871777 6.00E-11 Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups. NHGRI|-1
NM_005912 MC4R 19557197 http://www.ncbi.nlm.nih.gov/pubmed/19557197 Waist Circumference rs489693 4.00E-07 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. NHGRI|-1
NM_005912 MC4R 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs12970134 1.00E-12 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_005912 MC4R 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs12970134 5.00E-13 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_005912 MC4R 18454146 http://www.ncbi.nlm.nih.gov/pubmed/18454146 Waist Circumference rs12970134 2.00E-09 Common genetic variation near MC4R is associated with waist circumference and insulin resistance. NHGRI|-1
NM_005921 MAP3K1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs6867983 3.00E-06 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_005921 MAP3K1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs13362504 8.06E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_005921 MAP3K1 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs16886165 5.00E-07 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_005921 MAP3K1 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs889312 5.00E-09 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_005921 MAP3K1 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs889312 7.00E-20 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_005922 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1247555 1.91E-13 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_005922 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1247557 1.63E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_005922 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1620921 2.67E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_005922 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1740442 1.63E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_005922 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2115869 5.38E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_005922 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs783153 2.04E-15 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_005922 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1937479 3.04E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_005922 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2465868 1.54E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_005922 MAP3K4 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs935181 9.81E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_005923 MAP3K5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs911185 1.15E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_005923 MAP3K5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9321570 8.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_005923 MAP3K5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9494569 5.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_005923 MAP3K5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9483947 5.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_005923 MAP3K5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs3734552 1.62E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_005923 MAP3K5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs6919857 9.21E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_005923 MAP3K5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs3757167 7.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_005927 MFAP3 21701570 http://www.ncbi.nlm.nih.gov/pubmed/21701570 Body Mass Index rs2033195 6.00E-06 Genome-Wide Association of BMI in African Americans. NHGRI|-1
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2855812 2.55E-96 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005931 MICB 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs3134899 1.66E-06 NBL-GWAS version 1 dbGaP|2845
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2242955 1.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2246618 1.65E-78 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113461564 4.50E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2516400 4.45E-81 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005931 MICB 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs2516399 2.00E-12 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2516398 7.76E-78 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2844494 4.45E-80 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3131631 4.39E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005931 MICB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3131631 1.46E-15 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3131643 6.47E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_005931 MICB 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs12660382 1.96E-06 NBL-GWAS version 1 dbGaP|2845
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2395488 1.05E-104 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2395488 5.72E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2516424 8.37E-105 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2248617 1.68E-104 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3099844 7.98E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_005931 MICB 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3099844 8.62E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_005931 MICB 20662065 http://www.ncbi.nlm.nih.gov/pubmed/20662065 Lupus Vulgaris rs3099844 5.00E-10 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. NHGRI|-1
NM_005931 MICB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2905747 4.41E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_005931 MICB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2516415 4.45E-74 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_005932 MIPEP 21640322 http://www.ncbi.nlm.nih.gov/pubmed/21640322 Myopia rs9318086 2.00E-16 Genetic variants at 13q12.12 are associated with high myopia in the Han Chinese population. NHGRI|-1
NM_005932 MIPEP 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs753955 2.00E-12 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_005935 AFF1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs442177 3.00E-10 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_005941 MMP16 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs160441 8.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_005949 MT1F 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7194895 4.57E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_005950 MT1G 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7194895 4.57E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_005956 MTHFD1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs10498514 8.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_005956 MTHFD1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs2295639 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_005957 MTHFR 19597492 http://www.ncbi.nlm.nih.gov/pubmed/19597492 Atrial Fibrillation rs17375901 6.00E-07 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. NHGRI|-1
NM_005957 MTHFR 20031578 http://www.ncbi.nlm.nih.gov/pubmed/20031578 Homocysteine rs1801133 8.00E-35 "Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study." NHGRI|-1
NM_005957 MTHFR 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs17367504 2.00E-13 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_005958 MTNR1A 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, LDL" rs13148903 3.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_005959 MTNR1B 19060907 http://www.ncbi.nlm.nih.gov/pubmed/19060907 Blood Glucose rs10830963 3.00E-50 Variants in MTNR1B influence fasting glucose levels. NHGRI|-1
NM_005959 MTNR1B 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs10830963 6.00E-175 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_005959 MTNR1B 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs10830963 3.00E-43 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_005959 MTNR1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs1447352 5.90E-08 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_005959 MTNR1B 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Glucose rs1447352 6.00E-08 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_005959 MTNR1B 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs7950811 1.00E-08 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_005959 MTNR1B 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs7950811 9.00E-07 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_005959 MTNR1B 19060909 http://www.ncbi.nlm.nih.gov/pubmed/19060909 Blood Glucose rs1387153 2.00E-36 A variant near MTNR1B is associated with increased fasting plasma glucose levels and type 2 diabetes risk. NHGRI|-1
NM_005959 MTNR1B 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs1387153 8.00E-15 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_005959 MTNR1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs1387153 5.03E-07 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_005959 MTNR1B 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1387153 4.00E-11 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_005959 MTNR1B 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs1387153 2.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_005959 MTNR1B 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs1387153 8.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_005959 MTNR1B 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs10830956 5.00E-11 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_005959 MTNR1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs2166706 2.19E-06 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_005959 MTNR1B 19651812 http://www.ncbi.nlm.nih.gov/pubmed/19651812 Glucose rs2166706 2.00E-09 Common genetic variation near melatonin receptor MTNR1B contributes to raised plasma glucose and increased risk of type 2 diabetes among Indian Asians and European Caucasians. NHGRI|-1
NM_005961 MUC6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12146505 3.68E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_005962 MXI1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs716595 8.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_005962 MXI1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7917994 8.56E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_005962 MXI1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7921757 8.56E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_005966 NAB1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs10931468 2.00E-19 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_005969 NAP1L4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3814964 7.45E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_005969 NAP1L4 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs3847646 5.00E-06 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_005977 RNF6 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs9512144 6.15E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_005982 SIX1 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs10483727 9.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_005982 SIX1 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs10483727 1.00E-11 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_005986 SOX1 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs9555810 6.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_005986 SOX1 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs7333181 3.00E-08 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_005994 TBX2 20383145 http://www.ncbi.nlm.nih.gov/pubmed/20383145 Kidney Diseases rs8068318 3.00E-10 Genetic loci influencing kidney function and chronic kidney disease. NHGRI|-1
NM_005996 TBX3 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs1896312 3.00E-17 Genome-wide association study of PR interval. NHGRI|-1
NM_005996 TBX3 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs2384550 4.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_005996 TBX3 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs10850409 3.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_005996 TBX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10492258 6.91E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_005996 TBX3 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Tyrosine rs2194980 3.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_005996 TBX3 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs35444 1.00E-10 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_005996 TBX3 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs35444 8.00E-07 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_005996 TBX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs35444 7.12E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_005996 TBX3 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs11067228 2.00E-11 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_006003 UQCRFS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17691420 3.10E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_006003 UQCRFS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8110188 1.03E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006003 UQCRFS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8110188 6.42E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006003 UQCRFS1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs7250467 1.76E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_006005 WFS1 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs4689388 1.00E-08 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_006005 WFS1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs1801214 3.00E-08 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_006006 ZBTB16 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs17116334 9.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_006007 ZFAND5 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs11143230 7.00E-06 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_006007 ZFAND5 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs11143230 8.00E-07 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_006023 CDC123 20862305 http://www.ncbi.nlm.nih.gov/pubmed/20862305 "Diabetes Mellitus, Type 2" rs10906115 1.00E-08 Identification of new genetic risk variants for type 2 diabetes. NHGRI|-1
NM_006023 CDC123 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs12779790 1.00E-10 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_006023 CDC123 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11257695 1.67E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_006023 CDC123 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11257695 5.30E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_006033 LIPG 20031538 http://www.ncbi.nlm.nih.gov/pubmed/20031538 "Cholesterol, HDL" rs7240405 5.00E-10 Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions. NHGRI|-1
NM_006033 LIPG 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, HDL" rs4939883 2.00E-11 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_006033 LIPG 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs4939883 7.00E-15 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_006033 LIPG 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, HDL" rs2156552 2.00E-07 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_006033 LIPG 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs2156552 6.00E-12 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_006033 LIPG 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs2156552 2.00E-12 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_006034 TP53I11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7121790 1.34E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_006035 CDC42BPB 21471979 http://www.ncbi.nlm.nih.gov/pubmed/21471979 "Lymphoma, Large B-Cell, Diffuse" rs751837 3.00E-07 Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility. NHGRI|-1
NM_006038 SPATA2 18364390 http://www.ncbi.nlm.nih.gov/pubmed/18364390 Psoriasis rs495337 1.00E-08 Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene. NHGRI|-1
NM_006038 SPATA2 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs495337 2.00E-07 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_006040 HS3ST4 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs8049738 6.45E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_006042 HS3ST3A1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3785692 1.32E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_006042 HS3ST3A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs726800 4.58E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_006042 HS3ST3A1 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs10521232 4.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_006042 HS3ST3A1 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs4792394 9.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_006042 HS3ST3A1 19165918 http://www.ncbi.nlm.nih.gov/pubmed/19165918 "Lupus Erythematosus, Systemic" rs12949531 8.00E-06 Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. NHGRI|-1
NM_006042 HS3ST3A1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3944086 6.41E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_006043 HS3ST2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2239331 9.71E-06 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_006043 HS3ST2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2519974 4.99E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_006043 HS3ST2 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs8049603 1.00E-06 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_006049 SNAPC5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8684 5.35E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006058 TNIP1 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs2233287 5.00E-09 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_006058 TNIP1 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs10036748 2.00E-09 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_006058 TNIP1 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs17728338 1.00E-20 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NM_006059 LAMC3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs915401 4.11E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_006060 IKZF1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs12718597 5.00E-13 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_006060 IKZF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10248903 1.41E-06 NBL-GWAS version 2 dbGaP|2895
NM_006060 IKZF1 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs11978267 8.00E-11 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_006060 IKZF1 19684604 http://www.ncbi.nlm.nih.gov/pubmed/19684604 "Leukemia, Lymphoid" rs4132601 1.00E-19 "Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia." NHGRI|-1
NM_006060 IKZF1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs7805803 9.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_006060 IKZF1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs1456893 5.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_006060 IKZF1 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs4917014 3.00E-23 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_006060 IKZF1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs10276619 3.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_006068 TLR6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7696175 1.41E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_006079 CITED2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs628751 1.00E-17 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_006079 CITED2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs643381 5.00E-25 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_006079 CITED2 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs642858 2.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_006079 CITED2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs169291 5.93E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_006091 CORO2B 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs8030672 1.00E-11 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_006091 CORO2B 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs1445021 9.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_006091 CORO2B 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs11856323 1.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_006095 ATP8A1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs13139219 7.85E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_006106 YAP1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs2852894 1.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_006111 ACAA2 20031538 http://www.ncbi.nlm.nih.gov/pubmed/20031538 "Cholesterol, HDL" rs7240405 5.00E-10 Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions. NHGRI|-1
NM_006111 ACAA2 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, HDL" rs4939883 2.00E-11 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_006111 ACAA2 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs4939883 7.00E-15 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_006111 ACAA2 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, HDL" rs2156552 2.00E-07 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_006111 ACAA2 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs2156552 6.00E-12 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_006111 ACAA2 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs2156552 2.00E-12 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_006114 TOMM40 19125160 http://www.ncbi.nlm.nih.gov/pubmed/19125160 Alzheimer Disease rs157580 1.00E-40 Examination of the current top candidate genes for AD in a genome-wide association study. NHGRI|-1
NM_006114 TOMM40 21123754 http://www.ncbi.nlm.nih.gov/pubmed/21123754 Alzheimer Disease rs157580 1.00E-06 "Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort." NHGRI|-1
NM_006114 TOMM40 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs157580 8.00E-89 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_006114 TOMM40 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, HDL" rs157580 4.00E-07 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_006114 TOMM40 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs157580 2.00E-19 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_006114 TOMM40 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs157580 5.00E-08 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_006114 TOMM40 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs157580 4.96E-08 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_006114 TOMM40 20460622 http://www.ncbi.nlm.nih.gov/pubmed/20460622 Alzheimer Disease rs2075650 1.00E-295 Genome-wide analysis of genetic loci associated with Alzheimer disease. NHGRI|-1
NM_006114 TOMM40 21123754 http://www.ncbi.nlm.nih.gov/pubmed/21123754 Alzheimer Disease rs2075650 1.00E-06 "Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort." NHGRI|-1
NM_006114 TOMM40 19734902 http://www.ncbi.nlm.nih.gov/pubmed/19734902 Alzheimer Disease rs2075650 2.00E-157 Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. NHGRI|-1
NM_006114 TOMM40 19734903 http://www.ncbi.nlm.nih.gov/pubmed/19734903 Alzheimer Disease rs2075650 2.00E-16 Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. NHGRI|-1
NM_006114 TOMM40 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs2075650 3.00E-11 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_006114 TOMM40 20885792 http://www.ncbi.nlm.nih.gov/pubmed/20885792 Alzheimer Disease rs2075650 5.00E-36 Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. NHGRI|-1
NM_006114 TOMM40 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs2075650 3.00E-19 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_006114 TOMM40 18439552 http://www.ncbi.nlm.nih.gov/pubmed/18439552 C-Reactive Protein rs2075650 1.00E-07 Polymorphisms of the HNF1A gene encoding hepatocyte nuclear factor-1 alpha are associated with C-reactive protein. NHGRI|-1
NM_006114 TOMM40 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs2075650 1.05E-05 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_006114 TOMM40 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs2075650 8.00E-12 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_006114 TOMM40 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs2075650 1.81E-05 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_006117 PECI 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs6942328 1.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_006121 KRT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs14024 2.86E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_006122 MAN2A2 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2677744 1.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_006135 CAPZA1 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs17030613 1.00E-08 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_006135 CAPZA1 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs17030613 8.00E-06 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_006147 IRF6 20436469 http://www.ncbi.nlm.nih.gov/pubmed/20436469 Cleft Lip rs10863790 1.00E-14 A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. NHGRI|-1
NM_006147 IRF6 19270707 http://www.ncbi.nlm.nih.gov/pubmed/19270707 Cleft Lip rs642961 2.00E-06 Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. NHGRI|-1
NM_006154 NEDD4 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs8032158 6.00E-13 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_006157 NELL1 17684544 http://www.ncbi.nlm.nih.gov/pubmed/17684544 Crohn Disease rs1793004 3.00E-06 Systematic association mapping identifies NELL1 as a novel IBD disease gene. NHGRI|-1
NM_006157 NELL1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1987307 5.86E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_006157 NELL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs1670646 9.40E-05 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_006157 NELL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12295951 2.04E-05 NBL-GWAS version 2 dbGaP|2895
NM_006163 NFE2 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs10506328 5.00E-07 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_006167 NKX3-1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11776817 1.66E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_006167 NKX3-1 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs1512268 3.00E-30 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_006167 NKX3-1 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs1512268 4.00E-11 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_006169 NNMT 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs2847476 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_006169 NNMT 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2852438 5.77E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_006174 NPY5R 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs4691911 2.92E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_006176 NRGN 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs12807809 2.00E-09 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_006178 NSF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs183211 1.05E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_006178 NSF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs169201 1.25E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_006178 NSF 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs199533 1.00E-14 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_006178 NSF 20711177 http://www.ncbi.nlm.nih.gov/pubmed/20711177 Parkinson Disease rs199533 1.00E-06 Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. NHGRI|-1
NM_006178 NSF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs199533 5.05E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_006180 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1034042 1.58E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_006180 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769612 1.60E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_006180 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769605 9.38E-06 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_006180 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769600 1.35E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_006180 NTRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2769595 1.17E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_006180 NTRK2 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs2841498 4.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_006184 NUCB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs9676447 1.31E-06 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_006186 NR4A2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1918172 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_006186 NR4A2 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, HDL" rs16839962 9.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_006186 NR4A2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs17188434 1.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_006187 OAS3 21270382 http://www.ncbi.nlm.nih.gov/pubmed/21270382 Alcohol Drinking rs2072134 6.00E-17 Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men. NHGRI|-1
NM_006188 OCM2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs13438327 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_006195 PBX3 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs888219 2.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_006200 PCSK5 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs10512049 3.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_006200 PCSK5 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs12344488 5.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_006200 PCSK5 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2842483 5.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_006203 PDE4D 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs10052657 2.00E-19 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_006203 PDE4D 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs1823068 3.00E-08 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_006203 PDE4D 17667963 http://www.ncbi.nlm.nih.gov/pubmed/17667963 Neurotic Disorders rs702543 2.00E-06 A whole genome association study of neuroticism using DNA pooling. NHGRI|-1
NM_006203 PDE4D 19426955 http://www.ncbi.nlm.nih.gov/pubmed/19426955 Asthma rs1588265 3.00E-08 Genome-wide association analysis identifies PDE4D as an asthma-susceptibility gene. NHGRI|-1
NM_006206 PDGFRA 18193045 http://www.ncbi.nlm.nih.gov/pubmed/18193045 Body Height rs17690232 4.00E-07 Common variants in the GDF5-UQCC region are associated with variation in human height. NHGRI|-1
NM_006206 PDGFRA 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Count rs218237 2.00E-17 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_006206 PDGFRA 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs218237 3.00E-25 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_006206 PDGFRA 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs172629 1.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_006206 PDGFRA 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs2537859 4.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_006206 PDGFRA 21665993 http://www.ncbi.nlm.nih.gov/pubmed/21665993 Corneal Topography rs2114039 1.00E-09 Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore. NHGRI|-1
NM_006209 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7000665 1.12E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_006209 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9643136 1.15E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_006209 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6993464 6.39E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_006209 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11782176 5.55E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_006209 ENPP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6991756 5.01E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_006212 PFKFB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2243816 9.18E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_006226 PLCL1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs6738825 4.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_006226 PLCL1 18776929 http://www.ncbi.nlm.nih.gov/pubmed/18776929 Hip rs7595412 2.00E-06 Identification of PLCL1 gene for hip bone size variation in females in a genome-wide association study. NHGRI|-1
NM_006226 PLCL1 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs988583 6.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_006226 PLCL1 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs12617311 6.00E-13 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_006236 POU3F3 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs12615966 7.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_006238 PPARD 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs9658108 5.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_006238 PPARD 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs4713858 4.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_006240 PPEF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs239748 1.17E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_006243 PPP2R5A 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs351408 5.86E-06 NBL-GWAS version 1 dbGaP|2845
NM_006246 PPP2R5E 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs11158493 9.00E-07 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_006248 PRB2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs2908835 7.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_006253 PRKAB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7310266 5.81E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_006257 PRKCQ 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs11258747 1.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_006257 PRKCQ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1417032 1.94E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_006257 PRKCQ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2486866 1.53E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_006257 PRKCQ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2462692 1.57E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_006257 PRKCQ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11258317 5.61E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_006258 PRKG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7080306 9.57E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_006259 PRKG2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs710841 2.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_006259 PRKG2 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs710841 2.00E-08 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_006259 PRKG2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs788867 9.00E-28 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_006269 RP1 20364137 http://www.ncbi.nlm.nih.gov/pubmed/20364137 Intracranial Aneurysm rs9298506 1.00E-12 Genome-wide association study of intracranial aneurysm identifies three new risk loci. NHGRI|-1
NM_006269 RP1 18997786 http://www.ncbi.nlm.nih.gov/pubmed/18997786 Intracranial Aneurysm rs9298506 2.00E-09 Susceptibility loci for intracranial aneurysm in European and Japanese populations. NHGRI|-1
NM_006273 CCL7 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs3091315 2.00E-13 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_006277 ITSN2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2543662 5.11E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_006277 ITSN2 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs6707600 3.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_006278 ST3GAL4 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs4937126 5.00E-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_006282 STK4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs17322289 2.83E-05 NBL-GWAS version 2 dbGaP|2895
NM_006283 TACC1 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs7832232 5.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_006287 TFPI 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs7586970 9.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_006287 TFPI 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1520475 8.56E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_006290 TNFAIP3 19165918 http://www.ncbi.nlm.nih.gov/pubmed/19165918 "Lupus Erythematosus, Systemic" rs5029939 3.00E-12 Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. NHGRI|-1
NM_006290 TNFAIP3 20453841 http://www.ncbi.nlm.nih.gov/pubmed/20453841 "Arthritis, Rheumatoid" rs2230926 2.00E-06 A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. NHGRI|-1
NM_006290 TNFAIP3 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs2230926 1.00E-17 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_006290 TNFAIP3 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs610604 7.00E-07 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_006290 TNFAIP3 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs610604 9.00E-12 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NM_006290 TNFAIP3 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs2327832 4.00E-19 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_006290 TNFAIP3 17982456 http://www.ncbi.nlm.nih.gov/pubmed/17982456 "Arthritis, Rheumatoid" rs10499194 1.00E-09 Two independent alleles at 6q23 associated with risk of rheumatoid arthritis. NHGRI|-1
NM_006290 TNFAIP3 17982456 http://www.ncbi.nlm.nih.gov/pubmed/17982456 "Arthritis, Rheumatoid" rs6920220 1.00E-07 Two independent alleles at 6q23 associated with risk of rheumatoid arthritis. NHGRI|-1
NM_006290 TNFAIP3 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 "Arthritis, Rheumatoid" rs6920220 2.00E-09 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_006290 TNFAIP3 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs6920220 9.00E-13 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_006290 TNFAIP3 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6920220 8.00E-17 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_006296 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1016771 1.26E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_006296 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2043890 1.53E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_006296 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2717055 4.33E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_006296 VRK2 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs2312147 3.00E-07 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_006299 ZNF193 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs9380069 1.38E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_006299 ZNF193 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs967005 3.38E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_006299 ZNF193 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs9380064 3.75E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_006300 ZNF230 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs2191566 4.00E-07 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_006304 SHFM1 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs12669076 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_006304 SHFM1 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs17598306 9.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_006304 SHFM1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7781370 5.00E-12 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_006305 ANP32A 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs8030672 1.00E-11 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_006312 NCOR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7956328 6.36E-06 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_006312 NCOR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7956328 8.55E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_006313 USP15 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7313479 3.27E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_006317 BASP1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs682748 8.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_006322 TUBGCP3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs7992158 1.08E-04 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_006324 CFDP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs13337397 6.65E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_006325 RAN 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs7299940 7.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_006327 TIMM23 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7085433 6.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_006327 TIMM23 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7085433 7.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_006329 FBLN5 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs7153027 1.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_006333 C1D 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs724568 5.00E-06 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_006334 OLFM1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11790742 5.08E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_006334 OLFM1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11790027 5.11E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_006335 TIMM17A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2820304 2.55E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_006338 LRRN2 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs12143943 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_006342 TACC3 20348956 http://www.ncbi.nlm.nih.gov/pubmed/20348956 Urinary Bladder Neoplasms rs798766 1.00E-11 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_006342 TACC3 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs798766 4.00E-13 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_006348 COG5 20112360 http://www.ncbi.nlm.nih.gov/pubmed/20112360 Osteoarthritis rs3815148 8.00E-08 A genome-wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22. NHGRI|-1
NM_006352 ZNF238 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs10927101 2.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_006352 ZNF238 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs476141 1.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_006352 ZNF238 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1000543 1.25E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_006352 ZNF238 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2454222 6.14E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_006352 ZNF238 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2454221 8.28E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_006352 ZNF238 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2047137 9.15E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_006355 TRIM38 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs12216125 4.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_006357 UBE2E3 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs13010713 5.00E-11 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_006357 UBE2E3 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs1018326 2.00E-06 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_006357 UBE2E3 21041692 http://www.ncbi.nlm.nih.gov/pubmed/21041692 Heart Function Tests rs7602460 6.00E-06 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. NHGRI|-1
NM_006360 EIF3M 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs10767942 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_006360 EIF3M 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2450411 1.32E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_006364 SEC23A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17108400 4.63E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_006364 SEC23A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10483546 9.61E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_006364 SEC23A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs12432214 1.18E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_006366 CAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3777694 4.80E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_006377 UNC13B 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs10972341 9.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_006379 SEMA3C 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs4236644 2.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_006390 IPO8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs2046383 1.97E-04 Genome-wide association between genotype and incident heart failure in African-American participants dbGaP|2885
NM_006390 IPO8 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs2046383 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_006390 IPO8 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Aging rs1463605 7.00E-08 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_006393 NEBL 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs12219125 9.00E-09 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_006393 NEBL 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs12772794 7.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_006393 NEBL 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs16920624 7.00E-07 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_006393 NEBL 20610895 http://www.ncbi.nlm.nih.gov/pubmed/20610895 Vascular Diseases rs2359536 2.00E-06 Identification of evidence suggestive of an association with peripheral arterial disease at the OSBPL10 locus by genome-wide investigation in the Japanese population. NHGRI|-1
NM_006396 SSSCA1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs3782089 4.00E-13 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_006397 RNASEH2A 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7255045 2.00E-12 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_006398 UBD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3025652 6.81E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_006399 BATF 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs7155603 1.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_006401 ANP32B 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs4743150 5.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_006403 NEDD9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11751998 6.75E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_006404 PROCR 20231535 http://www.ncbi.nlm.nih.gov/pubmed/20231535 Blood Coagulation Factors rs867186 6.00E-37 "Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium." NHGRI|-1
NM_006404 PROCR 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs867186 4.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_006404 PROCR 20802025 http://www.ncbi.nlm.nih.gov/pubmed/20802025 Protein C rs867186 2.00E-200 Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. NHGRI|-1
NM_006409 ARPC1A 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs740160 2.00E-16 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_006411 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11553430 2.45E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006411 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130284 1.39E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006411 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130284 4.39E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006411 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3134945 1.24E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006411 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3134945 4.06E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006411 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3132965 8.39E-16 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_006411 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130349 5.68E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006411 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130349 9.28E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006411 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3134943 2.82E-105 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_006415 SPTLC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs7023075 1.47E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_006418 OLFM4 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Vitamin D rs10507577 3.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_006418 OLFM4 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs9536591 5.60E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_006418 OLFM4 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs9536591 6.00E-06 A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. NHGRI|-1
NM_006418 OLFM4 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs9536666 5.02E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_006437 PARP4 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs9581094 7.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_006437 PARP4 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2862909 1.03E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_006438 COLEC10 20548944 http://www.ncbi.nlm.nih.gov/pubmed/20548944 Osteoporosis rs2062375 3.00E-11 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. NHGRI|-1
NM_006438 COLEC10 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2062377 4.00E-16 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_006438 COLEC10 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs11995824 7.00E-09 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_006438 COLEC10 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs6469804 7.00E-15 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_006438 COLEC10 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs6993813 3.00E-11 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_006444 SMC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1867347 2.08E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_006446 SLCO1B1 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs4149056 7.00E-13 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_006446 SLCO1B1 18650507 http://www.ncbi.nlm.nih.gov/pubmed/18650507 Muscular Diseases rs4149056 2.00E-09 SLCO1B1 variants and statin-induced myopathy--a genomewide study. NHGRI|-1
NM_006446 SLCO1B1 21646302 http://www.ncbi.nlm.nih.gov/pubmed/21646302 Bilirubin rs4363657 5.00E-08 Mayo genome consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. NHGRI|-1
NM_006449 CDC42EP3 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs4670766 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_006449 CDC42EP3 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs17511102 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_006449 CDC42EP3 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs604381 8.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_006449 CDC42EP3 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs4670779 4.00E-06 New sequence variants associated with bone mineral density. NHGRI|-1
NM_006449 CDC42EP3 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs4352210 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_006457 PDLIM5 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs12500426 1.00E-11 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_006457 PDLIM5 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs17021918 4.00E-15 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_006459 ERLIN1 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs11597390 2.00E-08 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_006475 POSTN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1324038 2.34E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_006475 POSTN 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs1590305 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_006482 DYRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7980416 6.37E-05 NBL-GWAS version 2 dbGaP|2895
NM_006489 NOVA1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs1951082 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_006489 NOVA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1956817 6.56E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_006489 NOVA1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs17109831 6.25E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_006491 NOVA1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs1951082 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_006491 NOVA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1956817 6.56E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_006491 NOVA1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs17109831 6.25E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_006496 GNAI3 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs6537837 1.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_006510 TRIM27 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3131093 1.67E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_006514 SCN10A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs6795970 1.00E-58 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_006514 SCN10A 20062061 http://www.ncbi.nlm.nih.gov/pubmed/20062061 Electrocardiography rs6795970 3.00E-15 Genetic variation in SCN10A influences cardiac conduction. NHGRI|-1
NM_006514 SCN10A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs6795970 4.00E-09 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_006514 SCN10A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs6801957 3.00E-14 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_006514 SCN10A 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs6800541 2.00E-74 Genome-wide association study of PR interval. NHGRI|-1
NM_006514 SCN10A 21041692 http://www.ncbi.nlm.nih.gov/pubmed/21041692 Heart Function Tests rs6800541 5.00E-07 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. NHGRI|-1
NM_006514 SCN10A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9851724 6.00E-16 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_006516 SLC2A1 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs16830359 1.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_006529 GLRA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6824735 3.90E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_006531 IFT88 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Depressive Disorder rs7326068 3.00E-06 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_006534 NCOA3 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs6125048 2.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_006537 USP3 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs10519210 1.00E-08 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_006538 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_006538 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_006541 GLRX3 19786962 http://www.ncbi.nlm.nih.gov/pubmed/19786962 Speech Perception rs4751178 7.00E-06 First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. NHGRI|-1
NM_006541 GLRX3 21160409 http://www.ncbi.nlm.nih.gov/pubmed/21160409 HIV-1 rs4751185 7.00E-06 Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population. NHGRI|-1
NM_006546 IGF2BP1 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs9674544 2.00E-08 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_006546 IGF2BP1 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs9674544 8.00E-07 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_006547 IGF2BP3 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs12534093 2.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_006548 IGF2BP2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs4402960 1.00E-06 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_006548 IGF2BP2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs4402960 2.00E-09 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_006548 IGF2BP2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs4402960 8.00E-08 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_006548 IGF2BP2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs4402960 9.00E-16 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_006548 IGF2BP2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs4402960 9.00E-16 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_006548 IGF2BP2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs1470579 2.00E-09 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_006548 IGF2BP2 18711366 http://www.ncbi.nlm.nih.gov/pubmed/18711366 "Diabetes Mellitus, Type 2" rs6769511 1.00E-09 SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations. NHGRI|-1
NM_006548 IGF2BP2 21573907 http://www.ncbi.nlm.nih.gov/pubmed/21573907 "Diabetes Mellitus, Type 2" rs1374910 1.00E-07 "Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas." NHGRI|-1
NM_006552 SCGB1D1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2232932 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_006554 MTX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2969363 7.66E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_006555 YKT6 19060907 http://www.ncbi.nlm.nih.gov/pubmed/19060907 Blood Glucose rs4607517 1.00E-25 Variants in MTNR1B influence fasting glucose levels. NHGRI|-1
NM_006555 YKT6 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4607517 7.00E-92 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_006555 YKT6 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs4607517 2.00E-16 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_006557 DMRT2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs17641078 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_006561 CELF2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs3780993 6.86E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_006561 CELF2 21379329 http://www.ncbi.nlm.nih.gov/pubmed/21379329 Alzheimer Disease rs62209 2.00E-07 Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE. NHGRI|-1
NM_006566 CD226 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs763361 1.00E-08 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_006566 CD226 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs893001 1.00E-10 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_006567 FARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9328308 6.57E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_006568 CGRRF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4901519 7.56E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_006573 TNFSF13B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4772972 7.05E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_006577 B3GNT2 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs10865331 2.00E-19 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_006577 B3GNT2 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs10865331 7.00E-34 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_006595 API5 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs1484948 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_006595 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12273344 6.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_006595 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9300039 5.99E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_006595 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9300039 6.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_006595 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs10501281 5.29E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_006595 API5 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs7928165 3.27E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_006595 API5 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs10501293 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_006598 SLC12A7 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs4580814 5.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_006599 NFAT5 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1364063 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_006601 PTGES3 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs2958154 2.00E-06 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_006603 STAG2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs5910058 9.96E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_006614 CHL1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs6764363 6.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_006614 CHL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2272522 4.07E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_006614 CHL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs330891 4.78E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_006620 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs7775698 1.00E-14 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_006620 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs7775698 1.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_006620 HBS1L 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-56 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_006620 HBS1L 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7775698 3.00E-66 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_006620 HBS1L 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 5.00E-13 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_006620 HBS1L 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs7775698 8.00E-18 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_006620 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7776054 7.00E-69 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_006620 HBS1L 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs9399137 3.00E-36 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_006620 HBS1L 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Platelet Count rs9399137 1.00E-09 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_006620 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs9373124 7.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_006620 HBS1L 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs9373124 1.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_006620 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4895441 7.00E-86 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_006620 HBS1L 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs4895441 2.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_006620 HBS1L 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs9376092 2.00E-11 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_006620 HBS1L 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9402686 7.00E-42 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_006620 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs9494145 3.00E-15 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_006620 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Count rs9483788 1.00E-47 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_006620 HBS1L 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs9483788 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_006620 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 1.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_006620 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 3.00E-08 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_006620 HBS1L 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Count rs6569992 6.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_006622 PLK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1454909 4.31E-05 NBL-GWAS version 2 dbGaP|2895
NM_006622 PLK2 21190210 http://www.ncbi.nlm.nih.gov/pubmed/21190210 Obsessive-Compulsive Disorder rs1844437 2.00E-06 Genome-wide association study of hoarding traits. NHGRI|-1
NM_006627 POP4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs6509542 5.41E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_006627 POP4 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs10403021 2.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_006632 SLC17A3 18834626 http://www.ncbi.nlm.nih.gov/pubmed/18834626 Uric Acid rs1165205 4.00E-29 Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study. NHGRI|-1
NM_006632 SLC17A3 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs1408272 1.00E-11 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_006632 SLC17A3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1408272 4.00E-39 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_006632 SLC17A3 21149283 http://www.ncbi.nlm.nih.gov/pubmed/21149283 Iron-Regulatory Proteins rs1408272 9.00E-09 Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. NHGRI|-1
NM_006633 IQGAP2 20068591 http://www.ncbi.nlm.nih.gov/pubmed/20068591 Hearing Loss rs457717 4.00E-07 A genome-wide association study for age-related hearing impairment in the Saami. NHGRI|-1
NM_006640 9-Sep 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs9906155 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_006640 9-Sep 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs647861 5.97E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_006651 CPLX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs936551 5.29E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_006652 SPINT3 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs11696501 9.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_006654 FRS2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs10748128 2.00E-20 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_006654 FRS2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs11177669 3.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_006661 PDE10A 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs475061 1.23E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_006661 PDE10A 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs7762160 1.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_006661 PDE10A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1389923 7.18E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_006670 TPBG 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2917494 5.90E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_006671 SLC1A7 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs6695567 4.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_006671 SLC1A7 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1288331 3.44E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_006681 NMU 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4333263 1.12E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_006681 NMU 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs13120644 6.72E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6685931 1.42E-61 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6685931 2.61E-73 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1853883 1.08E-22 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1853883 4.85E-15 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7522952 2.34E-17 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7522952 5.97E-16 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1853882 4.26E-11 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1971579 3.43E-10 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7548070 2.60E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7548070 4.93E-21 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4915318 5.49E-30 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4915318 5.91E-34 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7538501 2.02E-20 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7538501 7.55E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922144 1.53E-32 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922144 3.90E-37 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6657442 1.30E-38 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6657442 2.07E-33 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7517126 5.99E-20 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs13375144 5.05E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006684 CFHR4 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs6428370 7.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801575 1.13E-19 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801575 7.31E-11 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_006684 CFHR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801575 8.31E-14 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_006690 MMP24 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs1555322 4.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_006703 NUDT3 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs206936 3.00E-08 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_006703 NUDT3 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs6918981 2.00E-08 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_006703 NUDT3 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Body Height rs6918981 3.00E-08 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_006705 GADD45G 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs10908907 6.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_006709 EHMT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs652888 1.56E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_006709 EHMT2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs652888 6.12E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_006709 EHMT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs652888 4.73E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006709 EHMT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7743807 8.09E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006709 EHMT2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs486416 8.91E-14 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006709 EHMT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs535586 1.21E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006709 EHMT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs659445 1.45E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006711 RNPS1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9796949 5.84E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_006722 MITF 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs922948 2.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_006724 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1247555 1.91E-13 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006724 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1247557 1.63E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006724 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1620921 2.67E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006724 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1740442 1.63E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006724 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2115869 5.38E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006724 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs783153 2.04E-15 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006724 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1937479 3.04E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006724 MAP3K4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2465868 1.54E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006724 MAP3K4 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs935181 9.81E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_006725 CD6 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs17824933 4.00E-09 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_006727 CDH10 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs2047267 4.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_006727 CDH10 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10076963 1.70E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_006727 CDH10 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs7727656 8.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_006727 CDH10 19456320 http://www.ncbi.nlm.nih.gov/pubmed/19456320 Autistic Disorder rs10038113 3.00E-06 A genome-wide association study of autism reveals a common novel risk locus at 5p14.1. NHGRI|-1
NM_006734 HIVEP2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6939141 1.97E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_006734 HIVEP2 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs9496398 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_006738 AKAP13 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs11858860 8.88E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_006738 AKAP13 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7171364 8.87E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_006738 AKAP13 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs383872 2.12E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_006738 AKAP13 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs338538 2.10E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_006738 AKAP13 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs6496932 1.00E-08 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_006756 TCEA1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs6473902 4.29E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_006757 TNNT3 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs909116 7.00E-07 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_006765 TUSC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6985300 4.38E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_006765 TUSC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1390052 8.02E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_006765 TUSC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1390053 7.02E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_006768 BRAP 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Alanine Transaminase rs3782886 5.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_006768 BRAP 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs11065987 1.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_006768 BRAP 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs11065987 1.00E-12 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_006769 LMO4 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 "Arthritis, Rheumatoid" rs983332 5.00E-06 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_006769 LMO4 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs2179965 1.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_006769 LMO4 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs7553864 3.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_006769 LMO4 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Eosinophils rs6576878 6.00E-06 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_006775 QKI 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 "Arthritis, Rheumatoid" rs10945919 3.00E-07 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_006775 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9356147 3.45E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006775 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs10428875 8.47E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006775 QKI 20516156 http://www.ncbi.nlm.nih.gov/pubmed/20516156 "Depressive Disorder, Major" rs4709845 9.00E-06 Genome-wide association study of major recurrent depression in the U.K. population. NHGRI|-1
NM_006775 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2201806 1.23E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006775 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6455970 2.15E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006775 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9459317 6.76E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006775 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1764053 5.00E-16 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006775 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1923608 7.61E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006775 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs16897566 2.75E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_006778 TRIM10 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs9468692 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_006778 TRIM10 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs9261535 1.70E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs6935269 1.42E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs7775397 2.58E-96 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_006781 C6orf10 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs7775397 1.11E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs6906662 2.11E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs544358 8.35E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs6910071 1.00E-299 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs574710 5.28E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs539703 1.19E-10 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs3132959 3.20E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs926591 9.71E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 20639878 http://www.ncbi.nlm.nih.gov/pubmed/20639878 Drug-Induced Liver Injury rs3129900 7.00E-25 A genome-wide study identifies HLA alleles associated with lumiracoxib-related liver injury. NHGRI|-1
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3129900 2.63E-37 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9368716 2.22E-15 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs4959093 6.77E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs910049 1.38E-188 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs910049 8.56E-23 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 18576341 http://www.ncbi.nlm.nih.gov/pubmed/18576341 "Arthritis, Juvenile Rheumatoid" rs2395148 2.00E-10 Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis. NHGRI|-1
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1265759 8.91E-105 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1265758 7.66E-98 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2894249 1.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2894249 4.64E-20 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2395150 6.15E-98 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs3129932 1.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3129932 5.76E-28 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3129934 2.60E-40 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 18941528 http://www.ncbi.nlm.nih.gov/pubmed/18941528 Multiple Sclerosis rs3129934 9.00E-11 "Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms." NHGRI|-1
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3129941 1.37E-197 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9268402 4.93E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9268403 3.54E-08 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs377763 9.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_006781 C6orf10 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs377763 1.50E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3134926 1.16E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3130299 1.19E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3115576 2.29E-10 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6936204 2.98E-22 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9267971 4.79E-12 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130311 1.54E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_006781 C6orf10 20595679 http://www.ncbi.nlm.nih.gov/pubmed/20595679 "Glomerulonephritis, IGA" rs3115573 1.00E-09 HLA has strongest association with IgA nephropathy in genome-wide analysis. NHGRI|-1
NM_006781 C6orf10 21505073 http://www.ncbi.nlm.nih.gov/pubmed/21505073 "Arthritis, Rheumatoid" rs9296015 2.00E-38 The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population. NHGRI|-1
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs6916062 2.52E-22 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9267992 2.98E-161 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_006781 C6orf10 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs3130320 3.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9268005 6.93E-161 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_006781 C6orf10 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs3130340 1.00E-07 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_006781 C6orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs926070 3.19E-161 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_006809 TOMM34 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1804644 1.27E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_006813 PNRC1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs12201676 4.00E-08 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_006814 PSMF1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6040222 7.79E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_006823 PKIA 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7821178 3.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_006823 PKIA 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs7846385 5.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_006823 PKIA 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs3864663 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_006823 PKIA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10091852 8.64E-05 NBL-GWAS version 2 dbGaP|2895
NM_006827 TMED10 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs910316 1.00E-07 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_006868 RAB31 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7228240 2.87E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_006871 RIPK3 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs1950500 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_006877 GMPR 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Lipids rs2142672 2.00E-08 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_006885 ZFHX3 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs16971384 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_006885 ZFHX3 19132087 http://www.ncbi.nlm.nih.gov/pubmed/19132087 Mucocutaneous Lymph Node Syndrome rs7199343 2.00E-06 A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease. NHGRI|-1
NM_006885 ZFHX3 19597491 http://www.ncbi.nlm.nih.gov/pubmed/19597491 Atrial Fibrillation rs7193343 1.00E-10 A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. NHGRI|-1
NM_006885 ZFHX3 19597492 http://www.ncbi.nlm.nih.gov/pubmed/19597492 Atrial Fibrillation rs2106261 2.00E-15 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. NHGRI|-1
NM_006887 ZFP36L2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2374459 6.50E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_006887 ZFP36L2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2374482 9.73E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_006888 CALM2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs815815 7.00E-07 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_006892 DNMT3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs437302 6.98E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_006898 HOXD3 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs2072590 5.00E-14 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_006899 IDH3B 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1810636 1.00E-10 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_006910 RBBP6 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs11643520 6.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_006912 RIT1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs2282301 7.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_006913 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3134945 1.24E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006913 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3134945 4.06E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006913 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3132965 8.39E-16 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_006913 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130349 5.68E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006913 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130349 9.28E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006913 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3134943 2.82E-105 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_006913 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs8365 1.09E-17 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_006914 RORB 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs11143609 7.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_006914 RORB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1398307 5.92E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_006917 RXRG 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs466639 1.00E-13 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_006917 RXRG 21368711 http://www.ncbi.nlm.nih.gov/pubmed/21368711 Personality rs285480 4.00E-07 Genome-wide association study of personality traits in bipolar patients. NHGRI|-1
NM_006917 RXRG 19754311 http://www.ncbi.nlm.nih.gov/pubmed/19754311 Acquired Immunodeficiency Syndrome rs10800098 4.00E-06 Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). NHGRI|-1
NM_006922 SCN3A 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Foot rs776488 2.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs438999 4.89E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs438999 5.68E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs437179 8.61E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs592229 4.34E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs429608 1.29E-22 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs429608 1.37E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs429608 2.03E-21 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs429608 2.63E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_006929 SKIV2L 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs429608 3.00E-21 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_006929 SKIV2L 20861866 http://www.ncbi.nlm.nih.gov/pubmed/20861866 Macular Degeneration rs429608 5.00E-15 Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration. NHGRI|-1
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs406936 1.64E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs406936 5.68E-09 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs454212 2.13E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs454212 5.99E-09 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs454212 3.78E-05 NBL-GWAS version 2 dbGaP|2895
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs453821 1.58E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_006929 SKIV2L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs453821 5.48E-09 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_006932 SMTN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs5753454 6.91E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_006940 SOX5 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs7979575 2.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_006940 SOX5 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs1464500 1.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_006940 SOX5 19754311 http://www.ncbi.nlm.nih.gov/pubmed/19754311 Acquired Immunodeficiency Syndrome rs1522232 2.00E-06 Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). NHGRI|-1
NM_006940 SOX5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs550338 8.88E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_006940 SOX5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11046688 4.39E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_006943 SOX12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6082956 6.19E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_006944 SPP2 20548944 http://www.ncbi.nlm.nih.gov/pubmed/20548944 Osteoporosis rs12151790 5.00E-07 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. NHGRI|-1
NM_006948 HSPA13 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs1006899 6.00E-06 New sequence variants associated with bone mineral density. NHGRI|-1
NM_006948 HSPA13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs8131875 7.83E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_006948 HSPA13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2178907 3.27E-05 NBL-GWAS version 2 dbGaP|2895
NM_006948 HSPA13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2822612 5.54E-05 NBL-GWAS version 2 dbGaP|2895
NM_006980 MTERF 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2974129 9.80E-07 NBL-GWAS version 1 dbGaP|2845
NM_006984 CLDN10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs870707 2.95E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_006987 RPH3AL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11869174 1.23E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_006987 RPH3AL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4247113 2.62E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_006987 RPH3AL 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4130140 2.30E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_006987 RPH3AL 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs7217319 4.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_006988 ADAMTS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2830551 1.12E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_006988 ADAMTS1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2830495 7.65E-06 NBL-GWAS version 1 dbGaP|2845
NM_006988 ADAMTS1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs229040 5.15E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_006996 SLC19A2 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs6687813 2.00E-14 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_006998 SCGN 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs932316 9.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_006999 PAPD7 18821564 http://www.ncbi.nlm.nih.gov/pubmed/18821564 Attention Deficit Disorder with Hyperactivity rs11134178 3.00E-06 Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder. NHGRI|-1
NM_006999 PAPD7 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs7729273 1.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_006999 PAPD7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6891243 2.10E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_007005 TLE4 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs2151145 1.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_007005 TLE4 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs12554086 4.00E-07 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_007005 TLE4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6559565 3.63E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_007005 TLE4 19714205 http://www.ncbi.nlm.nih.gov/pubmed/19714205 Asthma rs2378383 7.00E-07 Genome-wide association study implicates chromosome 9q21.31 as a susceptibility locus for asthma in mexican children. NHGRI|-1
NM_007007 CPSF6 20673876 http://www.ncbi.nlm.nih.gov/pubmed/20673876 "Depressive Disorder, Major" rs9943849 3.00E-06 "Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression." NHGRI|-1
NM_007023 RAPGEF4 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs6433379 1.00E-08 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_007023 RAPGEF4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs10187560 8.98E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_007026 DUSP14 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs712039 3.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_007027 TOPBP1 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs2718812 1.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_007028 TRIM31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113910808 3.53E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_007028 TRIM31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs1015465 3.69E-15 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_007028 TRIM31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9261434 1.75E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_007028 TRIM31 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs10947055 2.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_007028 TRIM31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4711209 1.03E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_007028 TRIM31 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs916570 1.10E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_007029 STMN2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11997947 9.55E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_007032 TRIOBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs16985637 3.13E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_007036 ESM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4865879 6.81E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_007036 ESM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10940434 3.27E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_007041 ATE1 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs10510102 2.00E-06 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_007045 FGFR1OP 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2301436 1.00E-12 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_007045 FGFR1OP 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs2301436 6.00E-08 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_007047 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9379858 6.21E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_007047 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9379859 3.79E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_007047 BTN3A2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs12176317 6.83E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_007049 BTN2A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs13195509 1.17E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_007049 BTN2A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs13195509 7.66E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_007049 BTN2A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9358946 1.12E-08 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_007049 BTN2A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs16891725 6.05E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_007050 PTPRT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2206426 9.22E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_007050 PTPRT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs941796 1.79E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_007050 PTPRT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs6016596 6.01E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_007050 PTPRT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12480143 2.99E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_007050 PTPRT 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2866823 1.63E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_007051 FAF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3827730 1.42E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_007051 FAF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3827730 4.08E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_007051 FAF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11205760 3.37E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_007053 CD160 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs1967017 4.00E-08 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_007053 CD160 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs12129861 3.00E-09 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_007057 ZWINT 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs4462262 9.00E-08 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_007057 ZWINT 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs35866326 4.02E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_007057 ZWINT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11005196 3.65E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_007057 ZWINT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11005240 4.15E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_007076 FICD 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs10861905 8.00E-07 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_007079 PTP4A3 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7839244 6.76E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_007105 SLC22A18AS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10832869 5.73E-05 NBL-GWAS version 2 dbGaP|2895
NM_007106 UBL3 20460270 http://www.ncbi.nlm.nih.gov/pubmed/20460270 Biliary Atresia rs9314986 2.00E-06 Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. NHGRI|-1
NM_007109 TCF19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3130453 2.06E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_007109 TCF19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3094187 3.73E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_007109 TCF19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7750641 5.60E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_007109 TCF19 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs7750641 7.36E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_007109 TCF19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9263794 9.83E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_007109 TCF19 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2073723 5.10E-08 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_007113 TCHH 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs11803731 3.00E-31 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_007120 UGT1A4 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs887829 1.00E-69 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_007120 UGT1A4 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs6742078 5E-324 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_007120 UGT1A4 21646302 http://www.ncbi.nlm.nih.gov/pubmed/21646302 Bilirubin rs4148325 5.00E-62 Mayo genome consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. NHGRI|-1
NM_007146 VEZF1 20802204 http://www.ncbi.nlm.nih.gov/pubmed/20802204 Multiple Sclerosis rs8074980 2.00E-06 Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. NHGRI|-1
NM_007149 ZNF184 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs10456051 3.75E-06 NBL-GWAS version 1 dbGaP|2845
NM_007149 ZNF184 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs12189640 1.22E-06 NBL-GWAS version 1 dbGaP|2845
NM_007161 LST1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9267502 3.79E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_007162 TFEB 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2842643 3.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_007163 SLC14A2 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Blood Urea Nitrogen rs4890568 2.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_007163 SLC14A2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs2243803 3.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_007163 SLC14A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6507618 7.92E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_007163 SLC14A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs8099273 6.66E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_007163 SLC14A2 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Albumins rs10502868 7.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_007166 PICALM 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs536841 3.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_007166 PICALM 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs561655 7.00E-11 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_007166 PICALM 19734902 http://www.ncbi.nlm.nih.gov/pubmed/19734902 Alzheimer Disease rs3851179 1.00E-09 Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. NHGRI|-1
NM_007169 PEMT 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs12936587 4.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_007177 FAM107A 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs13315591 5.00E-08 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_007179 INSL6 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 "Colitis, Ulcerative" rs10975003 1.00E-06 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_007180 TREH 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs4639966 1.00E-16 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_007180 TREH 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs10892279 1.00E-12 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_007184 NISCH 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6784615 4.00E-10 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_007186 CEP250 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs2236164 2.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_007194 CHEK2 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1547014 1.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_007194 CHEK2 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs738722 1.00E-08 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_007195 POLI 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs3730729 4.40E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_007200 AKAP13 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs11858860 8.88E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_007200 AKAP13 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7171364 8.87E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_007200 AKAP13 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs383872 2.12E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_007200 AKAP13 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs338538 2.10E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_007200 AKAP13 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs6496932 1.00E-08 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_007203 AKAP2 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs7032940 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_007207 DUSP10 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10495179 8.26E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_007207 DUSP10 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs11118864 2.88E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_007207 DUSP10 20972440 http://www.ncbi.nlm.nih.gov/pubmed/20972440 Colorectal Neoplasms rs6691170 1.00E-09 "Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33." NHGRI|-1
NM_007207 DUSP10 20972440 http://www.ncbi.nlm.nih.gov/pubmed/20972440 Colorectal Neoplasms rs6687758 2.00E-09 "Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33." NHGRI|-1
NM_007207 DUSP10 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs6687758 6.00E-08 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_007207 DUSP10 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs873549 6.00E-23 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_007207 DUSP10 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs12733856 3.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_007207 DUSP10 20971583 http://www.ncbi.nlm.nih.gov/pubmed/20971583 Dupuytren Contracture rs12032381 6.00E-06 Genome-wide association scan of Dupuytren's disease. NHGRI|-1
NM_007211 RASSF8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4963910 8.37E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_007216 HPS5 21124955 http://www.ncbi.nlm.nih.gov/pubmed/21124955 Serum Amyloid A Protein rs4353250 2.00E-51 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. NHGRI|-1
NM_007221 PMF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1052067 5.12E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_007226 NXPH2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs11681160 3.45E-07 NBL-GWAS version 1 dbGaP|2845
NM_007226 NXPH2 19478329 http://www.ncbi.nlm.nih.gov/pubmed/19478329 "Infertility, Male" rs1399645 9.00E-07 Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. NHGRI|-1
NM_007227 GPR45 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7584136 7.13E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_007227 GPR45 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs6712932 6.00E-06 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_007237 SP140 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs13397985 6.00E-10 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NM_007237 SP140 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs7423615 3.00E-13 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_007240 DUSP12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1063178 2.42E-05 NBL-GWAS version 2 dbGaP|2895
NM_007240 DUSP12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs3820449 3.23E-06 NBL-GWAS version 2 dbGaP|2895
NM_007240 DUSP12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12745240 8.04E-05 NBL-GWAS version 2 dbGaP|2895
NM_007240 DUSP12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1027702 2.71E-07 NBL-GWAS version 2 dbGaP|2895
NM_007241 SNF8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12941604 3.88E-05 NBL-GWAS version 2 dbGaP|2895
NM_007245 ATXN2L 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory Bowel Diseases rs8049439 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_007249 KLF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3764109 4.59E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_007249 KLF12 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs1886512 1.00E-08 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_007249 KLF12 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs8000245 8.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_007249 KLF12 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs12429889 5.00E-20 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_007249 KLF12 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs9600079 3.00E-09 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_007249 KLF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1411327 8.93E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_007249 KLF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9564966 5.86E-08 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_007249 KLF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs287553 5.17E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_007249 KLF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9543325 3.27E-11 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_007249 KLF12 20101243 http://www.ncbi.nlm.nih.gov/pubmed/20101243 Pancreatic Neoplasms rs9543325 3.00E-11 "A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33." NHGRI|-1
NM_007249 KLF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9318166 7.25E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_007249 KLF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12870000 1.29E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_007249 KLF12 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs1886449 9.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_007252 POU6F2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs9655034 8.80E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_007252 POU6F2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs859522 3.41E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_007256 SLCO2B1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2712800 1.72E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_007262 PARK7 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs35675666 5.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_007262 PARK7 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs12727642 9.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_007266 GPN1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs3749147 1.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_007308 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs3857059 3.60E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_007308 SNCA 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs2736990 2.00E-16 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_007308 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2736990 5.69E-09 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_007308 SNCA 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs2736990 7.00E-08 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_007308 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356188 8.41E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_007308 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs3775439 4.43E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_007308 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs894278 2.64E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_007308 SNCA 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs6532197 1.00E-07 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_007308 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4106153 9.18E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_007308 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1504489 8.42E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_007308 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12644119 2.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_007308 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356229 5.48E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_007308 SNCA 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs356219 2.00E-47 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_007308 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11931074 4.78E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_007308 SNCA 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson Disease rs11931074 7.00E-17 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_007308 SNCA 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs356220 2.00E-19 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_007308 SNCA 20711177 http://www.ncbi.nlm.nih.gov/pubmed/20711177 Parkinson Disease rs356220 3.00E-11 Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. NHGRI|-1
NM_007308 SNCA 21084426 http://www.ncbi.nlm.nih.gov/pubmed/21084426 Parkinson Disease rs356220 3.00E-08 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. NHGRI|-1
NM_007308 SNCA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356220 6.99E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_007308 SNCA 21044948 http://www.ncbi.nlm.nih.gov/pubmed/21044948 Parkinson Disease rs356220 9.00E-16 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. NHGRI|-1
NM_007312 HYAL1 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs11130248 5.00E-07 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_007313 ABL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1046129 9.47E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_007329 DMBT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7902878 9.49E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_007332 TRPA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2587562 4.42E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_007332 TRPA1 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs1963982 3.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_007332 TRPA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1835482 2.58E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_007332 TRPA1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2116078 3.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_007332 TRPA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs13258140 2.15E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_007343 PRSS3 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs216345 4.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_007344 TTF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1185995 1.06E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_007345 ZNF236 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4606813 1.02E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_007348 ATF6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4657121 4.49E-05 NBL-GWAS version 2 dbGaP|2895
NM_007348 ATF6 19772629 http://www.ncbi.nlm.nih.gov/pubmed/19772629 Parkinson Disease rs10918270 8.00E-06 Genomewide association study for onset age in Parkinson disease. NHGRI|-1
NM_007348 ATF6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12745240 8.04E-05 NBL-GWAS version 2 dbGaP|2895
NM_007349 PAXIP1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6952728 5.15E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_007350 PHLDA1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs7307780 5.00E-15 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_007351 MMRN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs3775478 6.07E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_007351 MMRN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs12233759 8.45E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_007351 MMRN1 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs6532197 1.00E-07 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_007353 GNA12 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs798502 3.00E-15 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_007353 GNA12 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs798497 7.00E-07 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_007353 GNA12 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs1182188 3.00E-09 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_007353 GNA12 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs798544 7.00E-15 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_007354 C3orf27 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs4328821 3.00E-17 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_007354 C3orf27 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs4328821 5.00E-40 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_007354 C3orf27 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Eosinophils rs4857855 9.00E-17 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_007358 MTF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10874753 4.57E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_007358 MTF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs660870 3.16E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_007358 MTF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs521428 4.57E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_007361 NID2 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Maximal Midexpiratory Flow Rate rs730532 6.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_007366 PLA2R1 21323541 http://www.ncbi.nlm.nih.gov/pubmed/21323541 "Glomerulonephritis, Membranous" rs4664308 9.00E-29 Risk HLA-DQA1 and PLA(2)R1 alleles in idiopathic membranous nephropathy. NHGRI|-1
NM_007370 RFC5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7295696 1.77E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_007374 SIX6 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2093210 6.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_012072 CD93 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs1984279 4.83E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_012072 CD93 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2153987 5.44E-06 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_012074 DPF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs12435382 1.24E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_012074 DPF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs12435412 1.27E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_012083 FRAT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs915196 6.30E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_012092 ICOS 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs4675374 6.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_012092 ICOS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7421114 9.89E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_012094 PRDX5 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs694739 4.00E-07 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_012094 PRDX5 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs694739 6.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_012102 RERE 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs4908760 7.00E-15 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_012102 RERE 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs12025126 6.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_012108 STAP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6826751 1.47E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_012108 STAP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6826751 2.81E-06 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_012108 STAP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1487383 5.45E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_012108 STAP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs3775866 1.06E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_012108 STAP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs3775866 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_012108 STAP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2242330 1.49E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_012108 STAP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2242330 2.00E-06 Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_012108 STAP1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2242330 3.42E-06 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_012108 STAP1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900791 7.74E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_012119 CDK20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10868677 8.79E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_012120 CD2AP 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs9349407 9.00E-09 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_012124 CHORDC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10765288 6.55E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_012124 CHORDC1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs12274302 4.00E-07 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_012124 CHORDC1 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Mortality rs1528753 8.00E-08 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_012124 CHORDC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4483549 1.63E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_012130 CLDN14 19561606 http://www.ncbi.nlm.nih.gov/pubmed/19561606 Kidney Calculi rs219780 4.00E-12 Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density. NHGRI|-1
NM_012131 CLDN17 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs9305406 8.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_012134 LMOD1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2820304 2.55E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_012137 DDAH1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1523993 6.03E-05 NBL-GWAS version 2 dbGaP|2895
NM_012152 LPAR3 18840781 http://www.ncbi.nlm.nih.gov/pubmed/18840781 "Diabetes Mellitus, Type 1" rs1983853 2.00E-06 Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes. NHGRI|-1
NM_012152 LPAR3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9729377 6.00E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_012153 EHF 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Antipsychotic Agents rs286913 7.00E-08 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_012153 EHF 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs5028798 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_012157 FBXL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2291897 1.82E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_012175 FBXO3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4756052 3.29E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_012177 FBXO5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs546599 2.19E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_012179 FBXO7 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9609565 4.00E-10 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_012183 FOXD3 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs17124318 6.00E-07 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_012183 FOXD3 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs17124318 4.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_012183 FOXD3 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs10493340 2.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_012190 ALDH1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs9851868 2.63E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_012194 C11orf41 21423239 http://www.ncbi.nlm.nih.gov/pubmed/21423239 "Suicide, Attempted" rs10437629 4.00E-06 A genome-wide association study of attempted suicide. NHGRI|-1
NM_012194 C11orf41 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs831620 3.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_012194 C11orf41 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2746600 8.29E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_012201 GLG1 18463975 http://www.ncbi.nlm.nih.gov/pubmed/18463975 Breast Neoplasms rs10871290 4.00E-07 A pilot genome-wide association study of early-onset breast cancer. NHGRI|-1
NM_012204 GTF3C4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17149524 4.12E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_012205 HAAO 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2374459 6.50E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_012205 HAAO 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2374482 9.73E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_012206 HAVCR1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs1501908 1.00E-11 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_012214 MGAT4A 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs12618769 1.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_012219 MRAS 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs2306374 3.00E-08 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_012219 MRAS 19198612 http://www.ncbi.nlm.nih.gov/pubmed/19198612 Coronary Artery Disease rs9818870 7.00E-13 New susceptibility locus for coronary artery disease on chromosome 3q22.3. NHGRI|-1
NM_012225 NUBP2 21216879 http://www.ncbi.nlm.nih.gov/pubmed/21216879 Insulin-Like Growth Factor Binding Protein 5 rs1065656 1.00E-11 A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. NHGRI|-1
NM_012229 NT5C2 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs11191548 4.00E-17 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_012229 NT5C2 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs11191548 7.00E-12 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_012229 NT5C2 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs11191548 7.00E-24 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_012231 PRDM2 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs2245218 2.13E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_012234 RYBP 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs9863706 4.00E-13 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_012234 RYBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10049211 5.35E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_012234 RYBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11128275 3.80E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_012234 RYBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6775777 2.36E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_012234 RYBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs13327342 3.68E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_012234 RYBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs13074688 3.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_012236 SCMH1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs6686842 2.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_012243 SLC35A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs7518943 1.96E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_012243 SLC35A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs495871 3.21E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_012243 SLC35A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs575323 3.32E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_012250 RRAS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11023186 9.66E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_012252 TFEC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1464776 1.55E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_012252 TFEC 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12673240 8.31E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_012253 TKTL1 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs766420 9.00E-09 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_012258 HEY1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11997947 9.55E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_012262 HS2ST1 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs7553864 3.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_012262 HS2ST1 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Eosinophils rs6576878 6.00E-06 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_012274 CXorf27 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs872690 9.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_012274 CXorf27 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs761913 5.02E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_012281 KCND2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs41943 1.61E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_012283 KCNG2 20801717 http://www.ncbi.nlm.nih.gov/pubmed/20801717 Amyotrophic Lateral Sclerosis rs4799088 9.00E-06 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. NHGRI|-1
NM_012283 KCNG2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs537962 1.39E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_012283 KCNG2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4799092 2.00E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_012293 PXDN 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs6735179 1.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_012294 RAPGEF5 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4719687 9.34E-07 NBL-GWAS version 1 dbGaP|2845
NM_012294 RAPGEF5 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs17364464 4.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_012294 RAPGEF5 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs1175000 5.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_012294 RAPGEF5 17903292 http://www.ncbi.nlm.nih.gov/pubmed/17903292 Thyrotropin rs10499559 8.00E-06 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_012294 RAPGEF5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs13227860 1.26E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_012296 GAB2 17553421 http://www.ncbi.nlm.nih.gov/pubmed/17553421 Alzheimer Disease rs2373115 1.00E-10 GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers. NHGRI|-1
NM_012296 GAB2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs10899489 8.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_012301 MAGI2 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs2691543 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_012301 MAGI2 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs11525066 3.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_012302 LPHN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10437024 2.02E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_012302 LPHN2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs11163585 9.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_012302 LPHN2 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Tumor Necrosis Factor-alpha rs7552393 5.00E-07 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_012302 LPHN2 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs7539409 1.00E-06 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_012307 EPB41L3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4798376 7.57E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_012307 EPB41L3 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11662763 5.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_012325 MAPRE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs437302 6.98E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_012329 MMD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4630612 4.47E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_012331 MSRA 21679298 http://www.ncbi.nlm.nih.gov/pubmed/21679298 Schizophrenia rs7017212 4.00E-06 A genome-wide association study for quantitative traits in schizophrenia in China. NHGRI|-1
NM_012331 MSRA 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs11775334 4.00E-06 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_012331 MSRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6992153 9.14E-05 NBL-GWAS version 2 dbGaP|2895
NM_012331 MSRA 20452100 http://www.ncbi.nlm.nih.gov/pubmed/20452100 Neurofibrillary Tangles rs11782819 3.00E-06 Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study. NHGRI|-1
NM_012331 MSRA 19557161 http://www.ncbi.nlm.nih.gov/pubmed/19557161 Adiposity rs545854 9.00E-09 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. NHGRI|-1
NM_012331 MSRA 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs545854 3.57E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_012335 MYO1F 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs4072910 4.00E-13 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_012340 NFATC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2143630 7.41E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_012351 OR10J1 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Hemoglobins rs4133289 2.00E-07 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_012351 OR10J1 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Chemokine CCL2 rs4128725 4.00E-12 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_012383 OSTF1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs10512049 3.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_012383 OSTF1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs12344488 5.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_012383 OSTF1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2842483 5.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_012385 NUPR1 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs4788084 3.00E-13 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_012387 PADI4 21452313 http://www.ncbi.nlm.nih.gov/pubmed/21452313 "Arthritis, Rheumatoid" rs2240335 2.00E-08 Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci. NHGRI|-1
NM_012387 PADI4 21505073 http://www.ncbi.nlm.nih.gov/pubmed/21505073 "Arthritis, Rheumatoid" rs2240335 2.00E-08 The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population. NHGRI|-1
NM_012396 PHLDA3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs16848610 1.93E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_012408 ZMYND8 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs11696358 9.43E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_012410 SEZ6L2 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Waist Circumference rs4787483 2.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_012411 PTPN22 17804836 http://www.ncbi.nlm.nih.gov/pubmed/17804836 "Arthritis, Rheumatoid" rs2476601 2.00E-11 TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. NHGRI|-1
NM_012411 PTPN22 19503088 http://www.ncbi.nlm.nih.gov/pubmed/19503088 "Arthritis, Rheumatoid" rs2476601 2.00E-21 "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis." NHGRI|-1
NM_012411 PTPN22 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs2476601 9.00E-74 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_012411 PTPN22 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2476601 1.00E-08 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_012411 PTPN22 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 "Diabetes Mellitus, Type 1" rs2476601 1.00E-07 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NM_012411 PTPN22 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs2476601 2.00E-80 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_012411 PTPN22 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2476601 9.00E-85 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_012411 PTPN22 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs2476601 1.00E-07 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_012413 QPCT 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs4352210 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_012413 QPCT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1158219 3.60E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_012416 RANBP6 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs1342326 9.00E-10 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_012417 PITPNC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2537828 3.82E-06 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_012419 RGS17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs487972 1.96E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_012446 SSBP2 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs410644 7.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_012452 TNFRSF13B 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Blood Proteins rs4273077 3.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_012452 TNFRSF13B 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs11867934 7.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_012453 TBL2 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs17145738 2.00E-12 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_012453 TBL2 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs17145738 7.00E-22 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_012454 TIAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7741028 7.77E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_012454 TIAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9384296 1.71E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_012454 TIAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12528887 1.25E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_012454 TIAM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12523857 1.25E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_012464 TLL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17689952 1.81E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_012465 TLL2 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs10786284 2.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_012470 TNPO3 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs12531711 9.00E-17 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_012470 TNPO3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs12531711 2.29E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_012470 TNPO3 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs12531711 6.00E-09 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_012470 TNPO3 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs10488631 4.00E-11 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_012470 TNPO3 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs10488631 2.00E-07 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_012470 TNPO3 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs10488631 3.00E-10 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_012470 TNPO3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 1.65E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_012470 TNPO3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10488631 2.48E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_012470 TNPO3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 2.00E-11 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_012470 TNPO3 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs10488631 7.00E-18 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_012470 TNPO3 20383147 http://www.ncbi.nlm.nih.gov/pubmed/20383147 "Scleroderma, Systemic" rs10488631 2.00E-13 Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. NHGRI|-1
NM_012470 TNPO3 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs10488631 4.00E-07 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_012471 TRPC5 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs7050529 6.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_012474 UCK2 19483681 http://www.ncbi.nlm.nih.gov/pubmed/19483681 Testicular Neoplasms rs4657482 2.00E-06 A genome-wide association study of testicular germ cell tumor. NHGRI|-1
NM_012479 YWHAG 21654844 http://www.ncbi.nlm.nih.gov/pubmed/21654844 Multiple Sclerosis rs7779014 8.00E-06 Genome-wide association study of severity in multiple sclerosis. NHGRI|-1
NM_012479 YWHAG 21654844 http://www.ncbi.nlm.nih.gov/pubmed/21654844 Multiple Sclerosis rs17149161 6.00E-06 Genome-wide association study of severity in multiple sclerosis. NHGRI|-1
NM_012479 YWHAG 21654844 http://www.ncbi.nlm.nih.gov/pubmed/21654844 Multiple Sclerosis rs7789940 6.00E-06 Genome-wide association study of severity in multiple sclerosis. NHGRI|-1
NM_012479 YWHAG 21654844 http://www.ncbi.nlm.nih.gov/pubmed/21654844 Multiple Sclerosis rs758944 8.00E-06 Genome-wide association study of severity in multiple sclerosis. NHGRI|-1
NM_012481 IKZF3 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs907092 8.00E-06 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_012481 IKZF3 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs9303277 2.00E-09 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_013227 ACAN 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs8041863 8.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_013231 FLRT2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs11624056 3.00E-08 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_013231 FLRT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1385397 5.84E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_013231 FLRT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2401711 9.82E-05 NBL-GWAS version 2 dbGaP|2895
NM_013231 FLRT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7152233 7.28E-06 NBL-GWAS version 2 dbGaP|2895
NM_013233 STK39 19114657 http://www.ncbi.nlm.nih.gov/pubmed/19114657 Blood Pressure rs6749447 2.00E-07 From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene. NHGRI|-1
NM_013238 DNAJC15 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs1324015 9.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_013240 N6AMT1 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs2832077 2.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_013243 SCG3 20159242 http://www.ncbi.nlm.nih.gov/pubmed/20159242 Asthma rs17525472 2.00E-06 Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. NHGRI|-1
NM_013248 NXT1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs1984279 4.83E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_013248 NXT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2153987 5.44E-06 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_013255 MKLN1 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs10265216 3.00E-06 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_013255 MKLN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6963574 3.99E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013262 MYLIP 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3757354 2.05E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_013263 BRD7 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs8054797 1.11E-08 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_013263 BRD7 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs8044151 6.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_013266 CTNNA3 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs16922827 1.00E-09 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_013266 CTNNA3 19187332 http://www.ncbi.nlm.nih.gov/pubmed/19187332 Asthma rs10762058 6.00E-06 Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis. NHGRI|-1
NM_013266 CTNNA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1948946 2.98E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_013266 CTNNA3 17158188 http://www.ncbi.nlm.nih.gov/pubmed/17158188 Tobacco Use Disorder rs4142041 6.00E-06 Novel genes identified in a high-density genome wide association study for nicotine dependence. NHGRI|-1
NM_013266 CTNNA3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4746675 2.46E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_013269 CLEC2D 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs3764021 5.00E-08 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_013272 SLCO3A1 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs3924426 2.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_013272 SLCO3A1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs7495052 3.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_013275 ANKRD11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2277908 3.47E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013283 MAT2B 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs6556756 5.00E-07 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_013283 MAT2B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2964318 3.61E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_013302 EEF2K 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs8058588 3.79E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_013322 SNX10 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4563785 4.83E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_013322 SNX10 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4563785 6.51E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_013322 SNX10 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4563785 3.60E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_013322 SNX10 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs886716 8.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_013330 NME7 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs16861990 2.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_013341 OLA1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11688834 1.04E-04 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_013347 RPA4 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs318173 9.69E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_013358 PADI1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2977310 5.28E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_013362 ZNF225 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs2061333 2.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_013367 ANAPC4 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs16877106 1.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_013367 ANAPC4 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Arthritis, Rheumatoid" rs3816587 9.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_013372 GREM1 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs1258763 1.00E-06 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_013372 GREM1 18372905 http://www.ncbi.nlm.nih.gov/pubmed/18372905 Colorectal Neoplasms rs4779584 5.00E-07 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. NHGRI|-1
NM_013373 ZDHHC8 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs613930 8.67E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_013374 PDCD6IP 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs11714343 9.59E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_013374 PDCD6IP 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1919624 4.01E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_013375 ABT1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9379897 1.45E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_013377 PDZRN4 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1458175 2.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_013377 PDZRN4 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1458175 7.90E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_013377 PDZRN4 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2220999 1.09E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_013377 PDZRN4 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 "Cholesterol, HDL" rs871392 3.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_013377 PDZRN4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11532502 1.30E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_013377 PDZRN4 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10880174 5.06E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_013377 PDZRN4 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10785303 5.06E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_013377 PDZRN4 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs1472402 8.20E-06 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_013377 PDZRN4 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs978797 3.38E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_013377 PDZRN4 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Alkaline Phosphatase rs1880887 1.00E-10 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_013380 ZFP112 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2609881 5.38E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_013381 TRHDE 21452313 http://www.ncbi.nlm.nih.gov/pubmed/21452313 "Arthritis, Rheumatoid" rs12831974 6.00E-06 Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci. NHGRI|-1
NM_013381 TRHDE 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs7963521 9.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NM_013381 TRHDE 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs1154865 7.00E-07 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_013396 USP25 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2823482 4.12E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_013396 USP25 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs2823357 6.00E-07 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_013396 USP25 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs2823455 9.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_013398 ZNF224 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs2061333 2.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_013402 FADS1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs174546 6.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_013402 FADS1 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs174546 1.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_013402 FADS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs174546 6.38E-06 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_013402 FADS1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs174547 2.00E-12 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_013402 FADS1 20037589 http://www.ncbi.nlm.nih.gov/pubmed/20037589 Electrocardiography rs174547 7.00E-179 A genome-wide perspective of genetic variation in human metabolism. NHGRI|-1
NM_013402 FADS1 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs174547 2.00E-09 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_013402 FADS1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs174547 2.00E-14 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_013402 FADS1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs174548 1.00E-12 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_013402 FADS1 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Phosphatidylcholines rs174548 5.00E-08 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_013402 FADS1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs174548 5.00E-14 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_013402 FADS1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs174550 2.00E-15 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_013402 FADS1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs174550 5.00E-13 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_013416 NCF4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4821544 1.71E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_013430 GGT1 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs4820599 4.00E-11 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_013430 GGT1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 gamma-Glutamyltransferase rs5751901 2.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_013433 TNPO2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs722571 8.62E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_013435 RAX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs9973180 9.04E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_013437 LRP12 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs16872085 1.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_013437 LRP12 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Benzodiazepines rs977396 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_013445 GAD1 18759275 http://www.ncbi.nlm.nih.gov/pubmed/18759275 Uric Acid rs4668338 3.00E-06 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. NHGRI|-1
NM_013450 BAZ2B 21738491 http://www.ncbi.nlm.nih.gov/pubmed/21738491 "Death, Sudden, Cardiac" rs4665058 2.00E-10 Identification of a Sudden Cardiac Death Susceptibility Locus at 2q24.2 through Genome-Wide Association in European Ancestry Individuals. NHGRI|-1
NM_013942 PAX3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs348970 1.96E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_013945 PAX7 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs12063142 5.00E-07 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_013956 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_013956 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_013956 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_013956 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013956 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013956 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013957 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_013957 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_013957 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_013957 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013957 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013957 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013958 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_013958 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_013958 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_013958 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013958 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013958 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013959 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_013959 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_013959 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_013959 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013959 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013959 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013960 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_013960 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_013960 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_013960 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013960 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013960 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013962 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_013962 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_013962 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_013962 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013962 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013962 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013964 NRG1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10503887 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_013964 NRG1 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs16879552 2.00E-08 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_013964 NRG1 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2439312 7.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_013964 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6989777 2.96E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013964 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4316112 2.73E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013964 NRG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4733132 4.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_013975 LIG3 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs2074518 6.00E-12 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_013976 GCDH 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs11085824 1.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9458255 9.49E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs992421 1.56E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs10755582 2.69E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6937817 1.71E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs12191995 7.53E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs17651062 1.03E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Lysine rs992037 1.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3019442 7.57E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3016563 5.39E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3016562 5.39E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9458363 1.15E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3019433 6.37E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3016557 2.75E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs3016539 7.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2022991 1.31E-22 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9365344 1.11E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1105056 3.72E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9456734 7.45E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9295184 3.26E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2846494 1.18E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2846488 3.07E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4636000 3.41E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2155510 6.56E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1012424 1.22E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9458611 5.98E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013987 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2803059 9.79E-13 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9458255 9.49E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs992421 1.56E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs10755582 2.69E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6937817 1.71E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs12191995 7.53E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs17651062 1.03E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Lysine rs992037 1.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3019442 7.57E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3016563 5.39E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3016562 5.39E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9458363 1.15E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3019433 6.37E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs3016557 2.75E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs3016539 7.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2022991 1.31E-22 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9365344 1.11E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1105056 3.72E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9456734 7.45E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9295184 3.26E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2846494 1.18E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2846488 3.07E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4636000 3.41E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2155510 6.56E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1012424 1.22E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9458611 5.98E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013988 PARK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2803059 9.79E-13 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264327 1.68E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2239518 3.45E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9468843 9.01E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3129975 2.40E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs12526186 1.27E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013993 DDR1 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs12526186 3.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_013993 DDR1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs6911628 2.20E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs4711229 5.43E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs3131043 1.76E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3131043 1.81E-11 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs34682678 1.68E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9295917 5.09E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs13198118 2.07E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264362 1.31E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013993 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs886424 4.70E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9295924 2.69E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs4713380 6.51E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs915664 8.45E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013993 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1264350 1.86E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7749924 2.25E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2535331 3.74E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2250264 8.16E-09 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013993 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2844659 1.23E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2535327 1.30E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844654 4.43E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264333 4.42E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264332 4.98E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264331 4.47E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013993 DDR1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs7756521 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_013993 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7756521 7.58E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264327 1.68E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2239518 3.45E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9468843 9.01E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3129975 2.40E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs12526186 1.27E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013994 DDR1 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs12526186 3.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_013994 DDR1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs6911628 2.20E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs4711229 5.43E-14 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs3131043 1.76E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3131043 1.81E-11 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs34682678 1.68E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9295917 5.09E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs13198118 2.07E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264362 1.31E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013994 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs886424 4.70E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9295924 2.69E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs4713380 6.51E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs915664 8.45E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013994 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1264350 1.86E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7749924 2.25E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2535331 3.74E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2250264 8.16E-09 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013994 DDR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2844659 1.23E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2535327 1.30E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844654 4.43E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264333 4.42E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264332 4.98E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264331 4.47E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_013994 DDR1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs7756521 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_013994 DDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7756521 7.58E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_014007 ZBTB43 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs867559 1.00E-07 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_014010 ASTN2 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs10983238 1.00E-07 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_014010 ASTN2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs3761845 8.63E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_014010 ASTN2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10817974 1.11E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_014010 ASTN2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs4838255 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_014010 ASTN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs17302884 5.16E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014011 SOCS5 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs76351433 2.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_014018 MRPS28 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2457401 3.30E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_014021 SSX2IP 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9729377 6.00E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_014023 WDR37 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Creatinine rs10794720 1.00E-08 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_014026 DCPS 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1695739 5.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_014031 SLC27A6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12523161 9.20E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_014034 ASF1A 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs11756438 5.00E-22 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_014043 CHMP2B 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs2660753 3.00E-08 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_014043 CHMP2B 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs9284813 5.00E-09 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_014043 CHMP2B 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs17181170 3.00E-08 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_014043 CHMP2B 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs7629490 1.00E-07 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_014055 IFT81 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Alpha-Globulins rs11065611 1.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2233967 9.71E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2233965 1.23E-10 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014068 PSORS1C1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2233956 1.05E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111358557 5.18E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs1265048 5.92E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs17190526 8.55E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6917517 4.73E-12 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014068 PSORS1C1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130981 9.90E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111573149 1.16E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1062470 8.99E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014068 PSORS1C1 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs3094212 7.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9295953 2.87E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112362740 7.54E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3094205 1.73E-15 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113742629 5.54E-13 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3778638 7.58E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112811551 5.79E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014068 PSORS1C1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs3815087 8.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_014068 PSORS1C1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130558 1.22E-10 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_014068 PSORS1C1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3131009 1.26E-10 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3823418 1.17E-33 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2074478 1.09E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014068 PSORS1C1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3130573 6.21E-15 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_014068 PSORS1C1 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs3130573 6.00E-10 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_014069 PSORS1C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2074478 1.09E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014069 PSORS1C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3130573 6.21E-15 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_014069 PSORS1C2 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs3130573 6.00E-10 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_014069 PSORS1C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9263733 3.63E-09 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112410690 1.88E-20 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2233967 9.71E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2233965 1.23E-10 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2233956 1.05E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111358557 5.18E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs1265048 5.92E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs17190526 8.55E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9262648 4.11E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9262651 7.50E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2394423 4.84E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9262656 4.80E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9380215 6.13E-23 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3130955 1.31E-20 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4947296 2.37E-23 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs3130544 1.62E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3130544 1.95E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_014070 C6orf15 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3130544 4.00E-15 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2517403 3.72E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2517403 3.96E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111785017 4.39E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2508011 3.21E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112687685 4.01E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 19620980 http://www.ncbi.nlm.nih.gov/pubmed/19620980 "Lymphoma, Follicular" rs6457327 5.00E-11 Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma. NHGRI|-1
NM_014070 C6orf15 20639881 http://www.ncbi.nlm.nih.gov/pubmed/20639881 "Lymphoma, Follicular" rs6457327 7.00E-06 Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. NHGRI|-1
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844635 2.76E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2844635 6.41E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9391709 1.38E-20 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014070 C6orf15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1265062 5.95E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014079 KLF15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs9851868 2.63E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_014112 TRPS1 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs4876662 2.00E-06 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_014112 TRPS1 18372905 http://www.ncbi.nlm.nih.gov/pubmed/18372905 Colorectal Neoplasms rs16892766 3.00E-18 A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3. NHGRI|-1
NM_014112 TRPS1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2044999 1.89E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_014112 TRPS1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1452747 8.94E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_014112 TRPS1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs7837448 7.95E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_014112 TRPS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12677395 2.30E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_014112 TRPS1 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs17658378 9.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_014141 CNTNAP2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs802568 2.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_014141 CNTNAP2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs7799181 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_014141 CNTNAP2 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Bone Density rs2214681 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_014141 CNTNAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10485843 9.23E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_014141 CNTNAP2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs7807268 4.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_014141 CNTNAP2 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs10487524 9.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_014141 CNTNAP2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1468375 1.41E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_014145 C20orf30 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs261360 3.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_014164 FXYD5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2285515 7.66E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014173 C19orf62 20852631 http://www.ncbi.nlm.nih.gov/pubmed/20852631 Breast Neoplasms rs8170 2.00E-09 A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population. NHGRI|-1
NM_014173 C19orf62 20852633 http://www.ncbi.nlm.nih.gov/pubmed/20852633 Ovarian Neoplasms rs8170 4.00E-06 Common variants at 19p13 are associated with susceptibility to ovarian cancer. NHGRI|-1
NM_014177 C18orf55 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3813108 9.00E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_014177 C18orf55 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10514115 6.18E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_014178 STXBP6 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs10147992 1.00E-08 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_014178 STXBP6 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs854384 1.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_014184 CNIH4 21042317 http://www.ncbi.nlm.nih.gov/pubmed/21042317 "Depressive Disorder, Major" rs11579964 4.00E-06 "Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned." NHGRI|-1
NM_014206 C11orf10 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs102275 6.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_014206 C11orf10 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs102275 2.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_014206 C11orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs102275 6.51E-06 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_014207 CD5 21244703 http://www.ncbi.nlm.nih.gov/pubmed/21244703 Multiple Sclerosis rs4939490 1.00E-09 Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data. NHGRI|-1
NM_014211 GABRP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17673653 9.07E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_014213 HOXD9 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs2592394 5.00E-07 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_014214 IMPA2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs7506045 7.07E-07 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_014214 IMPA2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs7506045 7.00E-07 A genome-wide genotyping study in patients with ischaemic stroke: initial analysis and data release. NHGRI|-1
NM_014217 KCNK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1377185 3.16E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_014217 KCNK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs556648 3.84E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_014223 NFYC 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4660456 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_014229 SLC6A11 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs12632101 2.55E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_014231 VAMP1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10492096 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_014243 ADAMTS3 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs7697556 2.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_014243 ADAMTS3 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs6816344 1.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_014244 ADAMTS2 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs10039254 8.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_014246 CELSR1 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs9615362 9.00E-09 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_014247 RAPGEF2 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs17291045 5.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_014265 ADAM28 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs10109414 1.00E-08 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_014268 MAPRE2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs595086 7.11E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_014270 SLC7A9 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Cystatin C rs12460876 3.00E-15 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_014270 SLC7A9 21572414 http://www.ncbi.nlm.nih.gov/pubmed/21572414 Metabolism rs8101881 6.00E-27 A genome-wide association study of metabolic traits in human urine. NHGRI|-1
NM_014271 IL1RAPL1 20838585 http://www.ncbi.nlm.nih.gov/pubmed/20838585 Triglycerides rs7890572 1.00E-07 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. NHGRI|-1
NM_014271 IL1RAPL1 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs5971305 8.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_014272 ADAMTS7 21239051 http://www.ncbi.nlm.nih.gov/pubmed/21239051 Cardiovascular Diseases rs1994016 5.00E-13 Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. NHGRI|-1
NM_014272 ADAMTS7 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs3825807 1.00E-12 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_014272 ADAMTS7 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs4380028 4.00E-09 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_014272 ADAMTS7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7164529 2.79E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_014272 ADAMTS7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7164529 5.00E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_014279 OLFM1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11790742 5.08E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_014279 OLFM1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11790027 5.11E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_014283 C1orf9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2859242 6.73E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_014285 EXOSC2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7852487 9.45E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_014285 EXOSC2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1046129 9.47E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_014292 CBX6 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs1014971 8.00E-12 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_014296 CAPN7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10510438 4.94E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_014302 SEC61G 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs2252586 8.00E-08 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_014313 TMEM50A 21700265 http://www.ncbi.nlm.nih.gov/pubmed/21700265 Blood Sedimentation rs3091242 2.00E-13 Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. NHGRI|-1
NM_014325 CORO1C 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs3825253 3.55E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_014329 EDC4 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs8060686 8.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_014331 SLC7A11 19165918 http://www.ncbi.nlm.nih.gov/pubmed/19165918 "Lupus Erythematosus, Systemic" rs2313132 8.00E-06 Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. NHGRI|-1
NM_014331 SLC7A11 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs2313982 1.85E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_014331 SLC7A11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1519337 3.54E-05 NBL-GWAS version 2 dbGaP|2895
NM_014333 CADM1 17903292 http://www.ncbi.nlm.nih.gov/pubmed/17903292 Albumins rs1712790 2.00E-06 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_014342 MTCH2 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs3817334 2.00E-12 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_014342 MTCH2 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs10838738 5.00E-09 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_014346 TBC1D22A 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs5766691 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_014346 TBC1D22A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11090762 9.31E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_014346 TBC1D22A 18821564 http://www.ncbi.nlm.nih.gov/pubmed/18821564 Attention Deficit Disorder with Hyperactivity rs9627183 3.00E-06 Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder. NHGRI|-1
NM_014361 CNTN5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2726363 6.62E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_014361 CNTN5 17903304 http://www.ncbi.nlm.nih.gov/pubmed/17903304 Atrial Fibrillation rs10501920 9.00E-06 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. NHGRI|-1
NM_014361 CNTN5 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs952700 6.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_014361 CNTN5 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs11212364 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_014361 CNTN5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1960997 9.62E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_014361 CNTN5 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs2405657 3.00E-06 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_014361 CNTN5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2155907 4.02E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_014361 CNTN5 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2509843 2.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_014361 CNTN5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2509843 4.70E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_014361 CNTN5 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs4237591 2.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_014363 SACS 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Interleukin-12 rs4770433 4.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_014363 SACS 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9507108 2.60E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_014363 SACS 20512145 http://www.ncbi.nlm.nih.gov/pubmed/20512145 Nasopharyngeal Neoplasms rs1572072 1.00E-08 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. NHGRI|-1
NM_014388 C1orf107 20436469 http://www.ncbi.nlm.nih.gov/pubmed/20436469 Cleft Lip rs10863790 1.00E-14 A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. NHGRI|-1
NM_014388 C1orf107 19270707 http://www.ncbi.nlm.nih.gov/pubmed/19270707 Cleft Lip rs642961 2.00E-06 Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. NHGRI|-1
NM_014393 STAU2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs12679254 2.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_014393 STAU2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs10283372 1.90E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_014394 GHITM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17689242 5.66E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_014394 GHITM 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs2224865 9.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_014394 GHITM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs2224865 9.98E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_014394 GHITM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11200376 6.80E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_014394 GHITM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11200394 6.80E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_014394 GHITM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12220373 6.80E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_014394 GHITM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11200700 1.00E-04 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_014394 GHITM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7068193 6.40E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_014394 GHITM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4615965 8.65E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_014394 GHITM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7906877 8.92E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_014395 DAPP1 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs11735070 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_014396 VPS41 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs11984145 6.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_014396 VPS41 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs859522 3.41E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_014398 LAMP3 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Bipolar Disorder rs683395 5.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_014398 LAMP3 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs11711441 8.00E-12 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_014405 CACNG4 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs17645023 6.00E-07 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_014421 DKK2 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Vital Capacity rs10516541 4.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_014421 DKK2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4956263 6.74E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_014421 DKK2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4956263 7.90E-06 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_014427 CPNE7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs154659 7.56E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_014427 CPNE7 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs154659 7.00E-08 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_014431 KIAA1274 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs10999409 5.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_014443 IL17B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17796714 1.02E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_014452 TNFRSF21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs2103868 4.69E-05 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_014452 TNFRSF21 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs2103868 5.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_014458 KLHL20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7550036 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_014458 KLHL20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7536773 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_014458 KLHL20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6692452 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_014461 CNTN6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12487870 3.85E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_014461 CNTN6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs11712183 6.06E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_014461 CNTN6 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs17047538 4.41E-06 NBL-GWAS version 1 dbGaP|2845
NM_014461 CNTN6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs17047538 8.54E-05 NBL-GWAS version 2 dbGaP|2895
NM_014461 CNTN6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs11714239 4.10E-05 NBL-GWAS version 2 dbGaP|2895
NM_014461 CNTN6 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs4684585 9.00E-07 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_014461 CNTN6 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs35964523 8.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_014461 CNTN6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs11131168 9.87E-05 NBL-GWAS version 2 dbGaP|2895
NM_014464 TINAG 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs16885294 4.00E-07 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_014478 CRCP 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs875971 4.00E-06 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_014480 ZNF544 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs260461 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_014482 BMP10 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs10496166 4.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_014483 RBMS3 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs1530057 3.00E-06 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_014483 RBMS3 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Bone Density rs10510628 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_014483 RBMS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6778464 1.22E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_014483 RBMS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9877517 6.53E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_014485 HPGDS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2059606 5.15E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_014487 ZNF330 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs17007017 7.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_014487 ZNF330 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs746484 6.98E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_014487 ZNF330 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9308140 5.26E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_014487 ZNF330 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4267812 6.73E-06 NBL-GWAS version 1 dbGaP|2845
NM_014487 ZNF330 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1550057 4.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_014498 GOLIM4 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs4345115 7.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_014503 UTP20 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Atherosclerosis rs10507130 7.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_014504 KCTD7 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs10263935 4.00E-07 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_014510 PCLO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2715148 1.46E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_014510 PCLO 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs2715148 1.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_014510 PCLO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2522833 1.54E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_014510 PCLO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2522840 2.85E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_014510 PCLO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2107828 5.11E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_014510 PCLO 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Mortality rs2371208 3.00E-06 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_014515 CNOT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs10506584 3.03E-05 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_014515 CNOT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1882191 7.52E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014517 UBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1807844 5.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014517 UBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1357540 2.69E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014518 ZNF229 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs1434579 4.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_014521 SH3BP4 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs11676855 9.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_014521 SH3BP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10167927 8.69E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_014521 SH3BP4 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs6736997 6.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_014521 SH3BP4 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs2042831 7.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_014522 PCDH11X 19136949 http://www.ncbi.nlm.nih.gov/pubmed/19136949 Alzheimer Disease rs2573905 2.00E-07 Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease. NHGRI|-1
NM_014550 CARD10 21307088 http://www.ncbi.nlm.nih.gov/pubmed/21307088 Optic Disk rs9607469 3.00E-12 "Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area." NHGRI|-1
NM_014553 TFCP2L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs12467309 2.59E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_014562 OTX1 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs6545977 5.00E-07 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_014564 LHX3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1747856 2.98E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_014567 BCAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs13337397 6.65E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_014569 ZKSCAN5 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs11761528 3.00E-36 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_014571 HEYL 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs12037222 6.00E-11 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_014575 SCHIP1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Waist Circumference rs2222328 8.00E-07 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_014581 OBP2B 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11244035 8.21E-10 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_014581 OBP2B 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs6597604 7.23E-06 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_014583 LMCD1 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Factor VII rs4591494 9.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_014586 HUNK 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs2833556 5.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_014586 HUNK 19890347 http://www.ncbi.nlm.nih.gov/pubmed/19890347 Vitiligo rs2833607 2.00E-06 "Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8." NHGRI|-1
NM_014586 HUNK 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs2833610 4.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_014586 HUNK 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1892577 7.73E-07 NBL-GWAS version 1 dbGaP|2845
NM_014592 KCNIP1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs11957313 9.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_014593 CXXC1 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs1036935 2.00E-06 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_014596 ZNRD1 19115949 http://www.ncbi.nlm.nih.gov/pubmed/19115949 Acquired Immunodeficiency Syndrome rs8321 5.00E-07 Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). NHGRI|-1
NM_014596 ZNRD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs8321 6.18E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_014600 EHD3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs647316 3.00E-11 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_014608 CYFIP1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs6606803 4.89E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_014616 ATP11B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11926120 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_014616 ATP11B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs6791663 3.29E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_014618 DBC1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs10984447 8.00E-06 Risk alleles for multiple sclerosis identified by a genomewide study. NHGRI|-1
NM_014618 DBC1 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs4837628 1.00E-06 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_014618 DBC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4642724 3.93E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_014618 DBC1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs16909449 1.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_014618 DBC1 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Cornea rs4837752 6.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_014618 DBC1 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Stomach Neoplasms rs876347 2.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_014618 DBC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1335258 1.77E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_014618 DBC1 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs1572299 4.00E-06 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_014618 DBC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10984107 4.62E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_014618 DBC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11789399 4.30E-06 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_014618 DBC1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11789399 6.00E-09 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_014618 DBC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11789399 1.60E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_014618 DBC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11789407 1.69E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_014618 DBC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11789407 2.17E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_014618 DBC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10759986 2.89E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_014618 DBC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10733631 2.07E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_014618 DBC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10759987 3.57E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_014618 DBC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7866602 5.24E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_014618 DBC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12237612 9.36E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_014622 VWA5A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs880321 7.55E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_014624 S100A6 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs4845552 6.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_014633 CTR9 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2018368 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_014633 CTR9 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11042937 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_014634 PPM1F 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs412050 6.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_014641 MDC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9262152 3.62E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_014643 ZNF516 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4891159 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_014643 ZNF516 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs3213875 9.37E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_014643 ZNF516 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7233038 3.43E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_014643 ZNF516 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11150911 7.69E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_014643 ZNF516 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1460277 1.50E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_014643 ZNF516 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2048135 2.86E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_014646 LPIN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2282636 5.94E-06 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_014646 LPIN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs3819090 2.10E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_014646 LPIN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs3826637 7.25E-06 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_014646 LPIN2 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs10460009 9.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_014650 ZNF432 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs6509616 8.33E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_014662 DEPDC5 21725309 http://www.ncbi.nlm.nih.gov/pubmed/21725309 "Hepatitis C, Chronic" rs1012068 1.00E-13 Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers. NHGRI|-1
NM_014667 VGLL4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs892932 6.66E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_014667 VGLL4 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs6782029 9.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_014671 UBE3C 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs6966038 4.00E-07 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_014671 UBE3C 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs6966038 5.00E-07 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_014672 KIAA0391 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10498331 1.12E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_014672 KIAA0391 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7144806 1.53E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_014672 KIAA0391 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6571697 2.02E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_014672 KIAA0391 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs12586317 2.00E-08 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_014673 TTC35 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11774379 9.01E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_014673 TTC35 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs4735076 1.93E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_014676 PUM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7536851 2.29E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_014676 PUM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10753241 2.20E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_014676 PUM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10753242 2.16E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_014676 PUM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7526662 1.86E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_014682 ST18 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10104090 4.42E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_014683 ULK2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs281357 2.51E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_014685 HERPUD1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs2217332 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_014685 HERPUD1 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs9989419 3.00E-31 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_014685 HERPUD1 20031538 http://www.ncbi.nlm.nih.gov/pubmed/20031538 "Cholesterol, HDL" rs9989419 9.00E-27 Genome-wide association analysis of high-density lipoprotein cholesterol in the population-based KORA study sheds new light on intergenic regions. NHGRI|-1
NM_014685 HERPUD1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs9989419 1.00E-32 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_014685 HERPUD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs9989419 2.21E-09 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_014685 HERPUD1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs173539 4.00E-75 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_014685 HERPUD1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs173539 5.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_014685 HERPUD1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs173539 1.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_014685 HERPUD1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs173539 9.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_014685 HERPUD1 20838585 http://www.ncbi.nlm.nih.gov/pubmed/20838585 Cardiovascular Diseases rs247616 1.00E-23 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. NHGRI|-1
NM_014685 HERPUD1 18454146 http://www.ncbi.nlm.nih.gov/pubmed/18454146 "Cholesterol, HDL" rs3764261 1.00E-27 Common genetic variation near MC4R is associated with waist circumference and insulin resistance. NHGRI|-1
NM_014685 HERPUD1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs3764261 1.00E-48 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_014685 HERPUD1 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs3764261 2.00E-57 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_014685 HERPUD1 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, HDL" rs3764261 7.00E-29 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_014685 HERPUD1 19359809 http://www.ncbi.nlm.nih.gov/pubmed/19359809 "Cholesterol, LDL" rs3764261 3.00E-12 Identification of genetic markers associated with high-density lipoprotein-cholesterol by genome-wide screening in a Japanese population: the Suita study. NHGRI|-1
NM_014685 HERPUD1 20686565 http://www.ncbi.nlm.nih.gov/pubmed/20686565 Lipids rs3764261 7E-380 "Biological, clinical and population relevance of 95 loci for blood lipids." NHGRI|-1
NM_014685 HERPUD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs3764261 6.97E-29 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_014685 HERPUD1 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs3764261 7.00E-07 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_014685 HERPUD1 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs3764261 7.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_014685 HERPUD1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs3764261 3.00E-13 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_014686 KIAA0355 20215924 http://www.ncbi.nlm.nih.gov/pubmed/20215924 Bipolar Disorder rs10407640 7.00E-06 A genome-wide association study of amygdala activation in youths with and without bipolar disorder. NHGRI|-1
NM_014688 USP6NL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7085769 1.11E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_014688 USP6NL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs4445554 7.16E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_014688 USP6NL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs10508425 1.56E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_014689 DOCK10 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs1517484 5.00E-07 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_014693 ECE2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs3914188 3.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_014694 ADAMTSL2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11507716 6.44E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_014697 NOS1AP 20062061 http://www.ncbi.nlm.nih.gov/pubmed/20062061 Electrocardiography rs1415259 7.00E-10 Genetic variation in SCN10A influences cardiac conduction. NHGRI|-1
NM_014697 NOS1AP 16648850 http://www.ncbi.nlm.nih.gov/pubmed/16648850 Electrocardiography rs10494366 1.00E-10 A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. NHGRI|-1
NM_014697 NOS1AP 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs10494366 5.00E-22 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_014697 NOS1AP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12140791 5.12E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_014697 NOS1AP 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs16857031 1.00E-34 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_014697 NOS1AP 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12029454 3.00E-45 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_014697 NOS1AP 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs4657178 7.00E-33 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_014697 NOS1AP 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs2880058 2.00E-10 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_014697 NOS1AP 19587794 http://www.ncbi.nlm.nih.gov/pubmed/19587794 "Arrhythmias, Cardiac" rs12143842 1.00E-83 Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies. NHGRI|-1
NM_014697 NOS1AP 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12143842 2.00E-78 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_014697 NOS1AP 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs12143842 2.00E-78 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_014707 HDAC9 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs615545 5.89E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_014713 LAPTM4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12471796 1.51E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_014713 LAPTM4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7565124 1.38E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_014713 LAPTM4A 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs7565124 2.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_014717 ZNF536 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs746961 8.00E-07 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_014720 SLK 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs7913069 9.00E-14 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_014721 PHACTR2 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs11155313 2.07E-05 Tier2a Allelic Association of Parkinson's Disease with Case-Unrelated Control Pairs dbGaP|2841
NM_014726 TBKBP1 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs8070463 5.00E-08 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_014728 FRMPD4 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4240151 7.26E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_014729 TOX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1463142 5.07E-05 NBL-GWAS version 2 dbGaP|2895
NM_014729 TOX 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs3110127 4.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_014729 TOX 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs6995588 2.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_014729 TOX 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs960089 6.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_014743 KIAA0232 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4626203 7.83E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_014746 RNF144A 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs771314 4.86E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_014746 RNF144A 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs6741819 2.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_014746 RNF144A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2352714 8.20E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_014746 RNF144A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7591430 5.64E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_014746 RNF144A 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs13008689 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_014747 RIMS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11208590 1.97E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_014747 RIMS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11208590 6.28E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_014749 KIAA0586 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3783698 1.53E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_014753 BMS1 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs2142991 3.00E-07 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_014753 BMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11239809 9.49E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_014753 BMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2256432 8.11E-06 NBL-GWAS version 2 dbGaP|2895
NM_014756 CKAP5 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs1007738 7.00E-07 New sequence variants associated with bone mineral density. NHGRI|-1
NM_014765 TOMM20 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs2069084 6.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_014767 SPOCK2 21216879 http://www.ncbi.nlm.nih.gov/pubmed/21216879 Insulin-Like Growth Factor I rs1245541 5.00E-07 A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. NHGRI|-1
NM_014772 KIAA0427 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs8091345 1.38E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_014772 KIAA0427 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs9952724 2.28E-10 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_014774 KIAA0494 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11583588 6.44E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_014776 GIT2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs2292354 7.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_014776 GIT2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11068997 7.24E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_014777 URB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs3811473 1.87E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_014777 URB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs3955545 1.80E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_014798 PLEKHM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11012 2.85E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_014798 PLEKHM1 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs11012 6.00E-08 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_014798 PLEKHM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11012 8.77E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_014799 HEPH 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs5965182 6.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_014800 ELMO1 17653210 http://www.ncbi.nlm.nih.gov/pubmed/17653210 Diabetic Nephropathies rs741301 8.00E-06 Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population. NHGRI|-1
NM_014800 ELMO1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs10488031 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_014800 ELMO1 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs4723619 3.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_014800 ELMO1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs6974491 2.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_014800 ELMO1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs6974491 4.00E-08 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_014800 ELMO1 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs11984075 5.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_014801 PCNXL2 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs12027542 4.00E-07 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_014808 FARP2 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs757978 2.00E-09 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_014809 KIAA0319 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs16889440 2.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_014814 PSMD6 19303062 http://www.ncbi.nlm.nih.gov/pubmed/19303062 Folic Acid rs153734 7.00E-06 "Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations." NHGRI|-1
NM_014818 TRIM66 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs4929923 1.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_014823 WNK1 19369658 http://www.ncbi.nlm.nih.gov/pubmed/19369658 Stroke rs12425791 1.00E-09 Genomewide association studies of stroke. NHGRI|-1
NM_014832 TBC1D4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11617463 4.45E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_014832 TBC1D4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9318312 3.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_014832 TBC1D4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10454657 2.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_014832 TBC1D4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9600419 2.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_014832 TBC1D4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1417549 1.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_014832 TBC1D4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4885263 3.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_014832 TBC1D4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1340900 5.20E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_014832 TBC1D4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1536284 5.20E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_014832 TBC1D4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1340902 6.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_014832 TBC1D4 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs548097 6.00E-07 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_014834 LRRC37A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2668692 3.94E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_014836 RHOBTB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4132554 7.66E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_014839 LPPR4 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs7543130 1.00E-07 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_014840 NUAK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs10861554 1.56E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_014840 NUAK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2251027 8.35E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_014845 FIG4 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs4947019 8.00E-06 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_014848 SV2B 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Sphingomyelins rs886144 2.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_014849 SV2A 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs11205277 1.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_014850 SRGAP3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2600178 1.52E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_014858 TMCC2 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs1668873 1.00E-20 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_014861 ATP2C2 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs10514604 8.00E-07 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_014862 ARNT2 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs2278702 6.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_014867 KBTBD11 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1043225 5.10E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_014869 IQSEC1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs765248 1.04E-04 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_014870 ZBTB40 20601957 http://www.ncbi.nlm.nih.gov/pubmed/20601957 Endometriosis rs16826658 2.00E-06 A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese. NHGRI|-1
NM_014870 ZBTB40 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs7521902 5.00E-06 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_014870 ZBTB40 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs7524102 1.00E-16 New sequence variants associated with bone mineral density. NHGRI|-1
NM_014870 ZBTB40 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs7524102 1.00E-06 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_014870 ZBTB40 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7524102 3.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_014870 ZBTB40 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs7524102 5.00E-16 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_014870 ZBTB40 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs7524102 9.00E-07 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_014870 ZBTB40 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs7524102 9.00E-09 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_014870 ZBTB40 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs7524102 2.00E-13 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_014870 ZBTB40 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs7524102 3.00E-07 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_014870 ZBTB40 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs6696981 2.00E-08 New sequence variants associated with bone mineral density. NHGRI|-1
NM_014870 ZBTB40 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs6426749 9.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_014882 ARHGAP25 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs10496166 4.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_014883 FAM13A 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs2869967 1.00E-07 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_014883 FAM13A 20173748 http://www.ncbi.nlm.nih.gov/pubmed/20173748 "Pulmonary Disease, Chronic Obstructive" rs7671167 1.00E-11 Variants in FAM13A are associated with chronic obstructive pulmonary disease. NHGRI|-1
NM_014883 FAM13A 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Cornea rs16996151 6.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_014888 FAM3C 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Bone Density rs7776725 1.00E-11 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_014888 FAM3C 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Bone Density rs7776725 2.00E-06 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_014889 PITRM1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs2764980 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_014889 PITRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17135017 4.32E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_014889 PITRM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11251836 2.88E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_014889 PITRM1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Bone Density rs2165468 1.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_014889 PITRM1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4881184 5.93E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_014892 RBM16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12528887 1.25E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_014892 RBM16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12523857 1.25E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_014897 ZNF652 21602798 http://www.ncbi.nlm.nih.gov/pubmed/21602798 Prostatic Neoplasms rs7210100 3.00E-13 Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21. NHGRI|-1
NM_014897 ZNF652 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs16948048 5.00E-09 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_014897 ZNF652 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs16948058 2.37E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_014900 COBLL1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs10221833 6.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_014900 COBLL1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs13424957 3.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_014900 COBLL1 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs10195252 4.00E-34 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_014903 NAV3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs1628326 7.94E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_014903 NAV3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs300483 1.05E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_014903 NAV3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1520799 3.08E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_014903 NAV3 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs1402279 5.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_014904 RAB11FIP2 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs2184898 3.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_014906 PPM1E 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs9303401 5.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_014906 PPM1E 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs16943326 4.30E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_014906 PPM1E 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs3809724 9.48E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_014910 ZNF507 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2867743 1.84E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_014911 AAK1 19772629 http://www.ncbi.nlm.nih.gov/pubmed/19772629 Parkinson Disease rs7577851 9.00E-06 Genomewide association study for onset age in Parkinson disease. NHGRI|-1
NM_014916 LMTK2 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs6465657 1.00E-09 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_014916 LMTK2 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs6465657 2.00E-08 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_014917 NTNG1 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs10494067 6.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_014921 LPHN1 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs4528684 1.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_014925 R3HDM2 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs1106766 2.00E-11 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_014926 SLITRK3 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs1523288 6.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_014927 CNKSR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11094807 2.92E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_014929 FASTKD2 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs2277912 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_014930 ZNF510 19030899 http://www.ncbi.nlm.nih.gov/pubmed/19030899 Body Height rs10816533 2.00E-06 Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci. NHGRI|-1
NM_014932 NLGN1 20516156 http://www.ncbi.nlm.nih.gov/pubmed/20516156 "Depressive Disorder, Major" rs13074924 9.00E-06 Genome-wide association study of major recurrent depression in the U.K. population. NHGRI|-1
NM_014940 MON1B 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs13330107 9.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_014951 ZNF365 21278746 http://www.ncbi.nlm.nih.gov/pubmed/21278746 Breast Neoplasms rs10995190 1.00E-09 Common variants in ZNF365 are associated with both mammographic density and breast cancer risk. NHGRI|-1
NM_014951 ZNF365 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs10995190 5.00E-15 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_014951 ZNF365 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs10995271 4.00E-20 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_014951 ZNF365 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs10761659 2.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_014951 ZNF365 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs10761659 4.00E-22 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_014951 ZNF365 17435756 http://www.ncbi.nlm.nih.gov/pubmed/17435756 Crohn Disease rs224136 1.00E-10 Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. NHGRI|-1
NM_014951 ZNF365 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs224136 1.23E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_014954 RPH3A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs11614063 9.92E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_014954 RPH3A 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs3803064 7.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_014960 ARSG 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1558878 3.50E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_014960 ARSG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11655081 5.18E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_014961 RUFY3 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7686646 9.64E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_014961 RUFY3 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs6815629 9.64E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_014970 KIFAP3 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs1541160 2.00E-08 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_014971 EFR3B 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs6733301 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_014978 SORCS3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs791116 5.67E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_014978 SORCS3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs791102 5.44E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_014979 SV2C 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12657643 5.44E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_014982 PCNX 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs36563 5.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_014983 HMGXB3 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs2304069 7.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_014984 AZI1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs7225354 9.76E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_014985 CEP152 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs17463995 4.89E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_015009 PDZRN3 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs11128347 6.00E-07 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9521061 1.33E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1041466 3.67E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1041466 4.00E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1411766 1.82E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1411766 8.15E-06 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17412858 2.11E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17412858 9.68E-06 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6492208 2.03E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6492208 7.41E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2391777 1.12E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2391777 3.42E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2391778 2.08E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2391778 8.33E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9515085 1.40E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9515085 4.40E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1411765 2.01E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1411765 8.24E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7989848 4.14E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7989848 7.02E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1929210 3.77E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9521445 1.21E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_015011 MYO16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9521445 2.95E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_015011 MYO16 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4772972 7.05E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_015021 ZNF292 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs1925690 3.00E-08 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_015024 XPO7 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs7843479 3.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_015025 MYT1L 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2241685 8.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_015025 MYT1L 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs10199521 3.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_015025 MYT1L 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs6735179 1.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_015027 PDXDC1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs1136001 7.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_015028 TNIK 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11920719 4.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_015028 TNIK 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs2088885 6.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_015028 TNIK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs13065441 3.16E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_015032 PDS5B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4942925 5.71E-05 NBL-GWAS version 2 dbGaP|2895
NM_015032 PDS5B 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs990324 5.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_015046 SETX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1185995 1.06E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_015047 KIAA0090 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs710865 1.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_015052 HECW1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17172185 8.52E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_015052 HECW1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17723330 6.14E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_015052 HECW1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs886550 1.17E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_015059 TLN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs938979 2.26E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_015059 TLN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12591037 3.67E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_015061 KDM4C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10815468 4.26E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_015061 KDM4C 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs4742269 5.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_015069 ZNF423 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs17281813 3.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_015071 ARHGAP26 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs27779 2.53E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_015071 ARHGAP26 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs245852 6.94E-05 NBL-GWAS version 2 dbGaP|2895
NM_015071 ARHGAP26 18759275 http://www.ncbi.nlm.nih.gov/pubmed/18759275 Uric Acid rs3776331 8.00E-06 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. NHGRI|-1
NM_015074 KIF1B 18997785 http://www.ncbi.nlm.nih.gov/pubmed/18997785 Multiple Sclerosis rs10492972 3.00E-10 Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis. NHGRI|-1
NM_015074 KIF1B 20676096 http://www.ncbi.nlm.nih.gov/pubmed/20676096 "Carcinoma, Hepatocellular" rs17401966 2.00E-18 Genome-wide association study identifies 1p36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers. NHGRI|-1
NM_015078 MCF2L2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7634425 2.97E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_015082 FSTL4 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs17166496 5.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_015082 FSTL4 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs1644305 8.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_015084 MRPS27 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs3213894 8.31E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_015084 MRPS27 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs17310329 5.79E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_015084 MRPS27 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs17376173 5.79E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_015085 RAP1GAP2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs12603284 3.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_015088 TNRC6B 19117981 http://www.ncbi.nlm.nih.gov/pubmed/19117981 Prostatic Neoplasms rs9623117 5.00E-07 Sequence variants at 22q13 are associated with prostate cancer risk. NHGRI|-1
NM_015088 TNRC6B 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs12484776 3.00E-12 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_015088 TNRC6B 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Body Height rs139909 2.00E-07 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_015088 TNRC6B 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs6001877 7.17E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_015091 FAM179B 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2899961 4.68E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_015093 TAB2 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs7772697 3.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_015093 TAB2 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Count rs636864 6.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_015093 TAB2 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Count rs727979 8.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_015097 CLASP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs12487660 2.70E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_015101 GLT25D2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2986574 2.05E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_015101 GLT25D2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2986574 9.22E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_015101 GLT25D2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs3010040 2.56E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_015101 GLT25D2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2296713 2.56E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_015101 GLT25D2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1887279 1.85E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_015101 GLT25D2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1887279 8.42E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_015101 GLT25D2 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs756199 7.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_015102 NPHP4 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Height rs7513590 5.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_015107 PHF8 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs7065696 4.00E-07 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_015123 FRMD4B 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs6806528 2.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_015123 FRMD4B 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs922948 2.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_015132 SNX13 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs10499504 4.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_015134 MPRIP 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs11867934 7.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_015135 NUP205 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs4294134 8.00E-10 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_015149 RGL1 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs4651156 3.00E-06 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_015149 RGL1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10797919 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_015150 RFTN1 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Optic Disk rs690037 2.00E-07 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_015150 RFTN1 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs12635698 5.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_015157 PHLDB1 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs498872 1.00E-08 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_015157 PHLDB1 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs498872 5.00E-11 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_015162 ACSBG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11072744 7.62E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_015162 ACSBG1 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Exploratory Behavior rs1533665 7.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_015168 ZC3H4 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs3810291 2.00E-12 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_015171 XPO6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs8051871 1.14E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_015173 TBC1D1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10517459 3.77E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_015180 SYNE2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7229 5.64E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_015183 MAST4 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1030231 9.35E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_015183 MAST4 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Nonalcoholic Fatty Liver Disease rs1697137 2.00E-06 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_015183 MAST4 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs10514995 1.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_015183 MAST4 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs10069397 5.00E-08 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_015184 PLCL2 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs1372072 2.00E-08 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_015186 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11145323 7.08E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_015186 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2150901 5.11E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_015186 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2183863 4.74E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_015186 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7030802 7.12E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_015186 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1574144 3.30E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_015187 SEL1L3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs6819016 1.61E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_015187 SEL1L3 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs959903 7.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_015192 PLCB1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs6056209 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_015194 MYO1D 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs225190 6.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_015198 COBL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs17578222 3.30E-05 NBL-GWAS version 2 dbGaP|2895
NM_015198 COBL 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs1012036 5.00E-06 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_015198 COBL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs10266118 2.46E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_015198 COBL 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs4948088 4.00E-08 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_015203 RPRD2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12029359 3.23E-05 NBL-GWAS version 2 dbGaP|2895
NM_015206 KIAA1024 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6495420 1.98E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_015207 OTUD3 20228798 http://www.ncbi.nlm.nih.gov/pubmed/20228798 "Colitis, Ulcerative" rs4654925 9.00E-22 Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). NHGRI|-1
NM_015207 OTUD3 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs6426833 2.00E-11 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_015207 OTUD3 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs6426833 2.00E-21 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_015207 OTUD3 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6426833 4.00E-35 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_015207 OTUD3 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs6426833 5.00E-13 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_015208 ANKRD12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1114591 3.23E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_015224 C3orf63 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs9835332 5.00E-13 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_015225 PRUNE2 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs10781380 7.00E-07 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_015226 CLEC16A 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs6498142 2.00E-07 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_015226 CLEC16A 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs11865121 2.00E-07 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_015226 CLEC16A 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs12708716 2.00E-16 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_015226 CLEC16A 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs12708716 3.00E-18 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_015226 CLEC16A 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs12708716 5.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_015226 CLEC16A 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs12708716 7.00E-13 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_015226 CLEC16A 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs12924729 3.00E-12 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_015226 CLEC16A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs998592 1.38E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_015226 CLEC16A 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 "Diabetes Mellitus, Type 1" rs2903692 7.00E-11 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NM_015226 CLEC16A 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6498169 4.00E-06 Risk alleles for multiple sclerosis identified by a genomewide study. NHGRI|-1
NM_015230 ARAP2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17457078 6.07E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_015230 ARAP2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs13109154 6.07E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_015230 ARAP2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs13120537 4.41E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_015230 ARAP2 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Piperazines rs17390445 1.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_015230 ARAP2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs16990598 8.28E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_015230 ARAP2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs16990620 8.26E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_015230 ARAP2 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 "Arthritis, Rheumatoid" rs437943 4.00E-06 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_015230 ARAP2 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs1533317 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_015233 MTUS2 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Attention Deficit Disorder with Hyperactivity rs1161463 2.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_015236 LPHN3 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs6856328 8.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_015236 LPHN3 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs2172802 3.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_015239 AGTPBP1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7048878 9.89E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_015242 ARAP1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs1552224 1.00E-22 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_015243 VPS13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4735627 2.26E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_015245 ANKS1A 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs2140418 4.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_015245 ANKS1A 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs17609940 1.00E-08 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_015247 CYLD 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs8060598 3.34E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_015247 CYLD 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs10521222 9.00E-13 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_015252 EHBP1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2710638 4.99E-07 NBL-GWAS version 1 dbGaP|2845
NM_015252 EHBP1 18264098 http://www.ncbi.nlm.nih.gov/pubmed/18264098 Prostatic Neoplasms rs721048 8.00E-09 Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. NHGRI|-1
NM_015253 WSCD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs8069938 4.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_015253 WSCD1 20876614 http://www.ncbi.nlm.nih.gov/pubmed/20876614 "Carcinoma, Non-Small-Cell Lung" rs9303196 8.00E-06 A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population. NHGRI|-1
NM_015259 ICOSLG 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs4819388 2.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_015259 ICOSLG 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2838519 6.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_015259 ICOSLG 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs762421 1.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_015261 NCAPD3 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs1031381 6.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_015263 DMXL2 20159242 http://www.ncbi.nlm.nih.gov/pubmed/20159242 Asthma rs17525472 2.00E-06 Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. NHGRI|-1
NM_015265 SATB2 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs1992950 5.00E-06 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_015265 SATB2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs12617311 6.00E-13 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_015267 CUX2 21270382 http://www.ncbi.nlm.nih.gov/pubmed/21270382 Alcohol Drinking rs12229654 4.00E-35 Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men. NHGRI|-1
NM_015271 TRIM2 21654844 http://www.ncbi.nlm.nih.gov/pubmed/21654844 Multiple Sclerosis rs12644284 4.00E-06 Genome-wide association study of severity in multiple sclerosis. NHGRI|-1
NM_015275 KIAA1033 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1663563 9.14E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_015277 NEDD4L 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs17064520 3.22E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_015277 NEDD4L 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs8099014 6.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_015278 SASH1 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic Nephropathies rs6930576 7.00E-07 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_015278 SASH1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Insulin rs6930337 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_015278 SASH1 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs9390537 8.00E-06 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_015278 SASH1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs9497975 7.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_015285 WDR7 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1557351 4.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_015288 PHF15 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs13187289 2.00E-10 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_015293 SYNE1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs2673776 8.05E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_015293 SYNE1 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs17082664 1.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_015293 SYNE1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs17082664 4.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_015293 SYNE1 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs7747960 9.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_015293 SYNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2623963 7.61E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_015293 SYNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7745725 1.87E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_015293 SYNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1358317 1.61E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_015293 SYNE1 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs1322512 8.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_015294 TRIM37 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs3809724 9.48E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_015303 VPS8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10937194 5.90E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_015306 USP24 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs12239436 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_015306 USP24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17111925 2.46E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_015306 USP24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17111925 6.56E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_015310 PSD3 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4921617 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_015310 PSD3 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4646249 7.28E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_015310 PSD3 21572414 http://www.ncbi.nlm.nih.gov/pubmed/21572414 Metabolism rs4921914 1.00E-28 A genome-wide association study of metabolic traits in human urine. NHGRI|-1
NM_015310 PSD3 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs1495741 4.00E-11 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_015312 KIAA1109 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs13151961 2.00E-27 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_015312 KIAA1109 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs4505848 5.00E-13 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_015312 KIAA1109 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs6534347 2.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_015312 KIAA1109 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs13119723 7.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_015315 LARP1 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs13165478 7.00E-14 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_015315 LARP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7731137 9.50E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_015317 PUM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1043419 4.16E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_015321 CRTC1 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs10423674 6.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_015325 KIAA0947 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs256481 6.79E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_015325 KIAA0947 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Survival rs32566 2.00E-09 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_015325 KIAA0947 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs7728043 1.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_015325 KIAA0947 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs13187879 1.23E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_015325 KIAA0947 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7723605 5.65E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_015325 KIAA0947 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2964459 5.40E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_015326 SRGAP2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2336938 2.83E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_015328 AHCYL2 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs7787531 9.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_015335 MED13L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs11611238 6.15E-05 NBL-GWAS version 2 dbGaP|2895
NM_015345 DAAM2 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs2395730 8.00E-08 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_015353 KCTD2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs11077773 8.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_015358 MORC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2835340 1.19E-05 NBL-GWAS version 2 dbGaP|2895
NM_015358 MORC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs218626 4.70E-05 NBL-GWAS version 2 dbGaP|2895
NM_015361 R3HDM1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs313519 3.35E-06 NBL-GWAS version 1 dbGaP|2845
NM_015361 R3HDM1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs313528 4.29E-06 NBL-GWAS version 1 dbGaP|2845
NM_015367 BCL2L13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9604779 5.29E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_015376 RASGRP3 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs13385731 1.00E-15 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_015381 FAM19A5 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs130110 4.58E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_015381 FAM19A5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs78492 4.91E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_015381 FAM19A5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11090762 9.31E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_015381 FAM19A5 18821564 http://www.ncbi.nlm.nih.gov/pubmed/18821564 Attention Deficit Disorder with Hyperactivity rs9627183 3.00E-06 Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder. NHGRI|-1
NM_015397 DCAF12 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs7871764 2.00E-06 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_015398 FAM149A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2276919 4.19E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_015423 AASDHPPT 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs10895959 3.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_015425 POLR1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2288118 2.11E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_015425 POLR1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs10779967 5.61E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_015431 TRIM58 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs11204538 2.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_015435 RNF19A 21041692 http://www.ncbi.nlm.nih.gov/pubmed/21041692 Heart Function Tests rs1371867 9.00E-06 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. NHGRI|-1
NM_015440 MTHFD1L 20885792 http://www.ncbi.nlm.nih.gov/pubmed/20885792 Alzheimer Disease rs11754661 2.00E-10 Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. NHGRI|-1
NM_015440 MTHFD1L 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs6922269 3.00E-08 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_015441 OLFML2B 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs2880058 2.00E-10 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_015441 OLFML2B 19587794 http://www.ncbi.nlm.nih.gov/pubmed/19587794 "Arrhythmias, Cardiac" rs12143842 1.00E-83 Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies. NHGRI|-1
NM_015441 OLFML2B 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12143842 2.00E-78 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_015441 OLFML2B 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs12143842 2.00E-78 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_015443 KIAA1267 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2532274 2.22E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_015443 KIAA1267 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2532269 2.70E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_015443 KIAA1267 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2668692 3.94E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_015453 THUMPD3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2600178 1.52E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_015455 CNOT6 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs10464059 3.00E-06 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_015458 MTMR9 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Nonalcoholic Fatty Liver Disease rs2251301 1.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_015460 MYRIP 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs9985399 9.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_015460 MYRIP 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs6599077 1.00E-07 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_015461 ZNF521 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs1840440 3.00E-07 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_015463 CNRIP1 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Sphingomyelins rs9309413 2.00E-09 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_015464 SOSTDC1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs10270805 9.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_015472 WWTR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10513355 4.66E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_015477 SIN3A 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs8028182 3.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_015480 PVRL3 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs76884941 1.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_015480 PVRL3 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs56238310 1.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_015482 SLC22A23 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs4959235 2.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NM_015482 SLC22A23 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs17309827 7.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_015484 SYF2 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs11249215 9.00E-11 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_015484 SYF2 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs10903122 2.00E-10 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_015485 RWDD3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1858111 4.19E-06 NBL-GWAS version 1 dbGaP|2845
NM_015485 RWDD3 19207018 http://www.ncbi.nlm.nih.gov/pubmed/19207018 Pain Measurement rs6693882 2.00E-06 Genome-wide association study of acute post-surgical pain in humans. NHGRI|-1
NM_015485 RWDD3 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1414896 2.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_015503 SH2B1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs7498665 3.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_015503 SH2B1 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs7498665 5.00E-11 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_015503 SH2B1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7498665 1.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_015503 SH2B1 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs7359397 2.00E-20 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_015508 TIPARP 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs2665390 3.00E-07 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_015514 NGDN 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs223116 3.00E-08 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_015515 KRT23 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs2315504 8.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_015516 TSKU 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs873108 5.54E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_015520 MAGI1 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6795735 2.00E-16 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_015520 MAGI1 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs4607103 1.00E-08 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_015520 MAGI1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10510933 3.46E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_015525 IBTK 21606135 http://www.ncbi.nlm.nih.gov/pubmed/21606135 Coronary Artery Disease rs16893526 5.00E-06 A Genome-wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease. NHGRI|-1
NM_015530 GORASP2 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs4668356 5.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_015530 GORASP2 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs4668356 1.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_015530 GORASP2 18759275 http://www.ncbi.nlm.nih.gov/pubmed/18759275 Uric Acid rs4668338 3.00E-06 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. NHGRI|-1
NM_015532 GRINL1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs597804 5.59E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_015532 GRINL1A 19609347 http://www.ncbi.nlm.nih.gov/pubmed/19609347 Hypertension rs1550576 3.00E-06 A genome-wide association study of hypertension and blood pressure in African Americans. NHGRI|-1
NM_015535 SPATS2L 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs1569175 9.00E-07 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_015535 SPATS2L 19727025 http://www.ncbi.nlm.nih.gov/pubmed/19727025 Exercise rs12612420 8.00E-06 Genome-wide association study of exercise behavior in Dutch and American adults. NHGRI|-1
NM_015541 LRIG1 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs2242285 1.00E-08 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_015544 TMEM98 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9904938 7.03E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_015548 DST 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12663282 4.56E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_015548 DST 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9475671 1.07E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_015556 SIPA1L1 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11848785 1.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_015559 SETBP1 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs991014 6.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_015559 SETBP1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs616444 9.00E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_015559 SETBP1 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs2243803 3.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_015559 SETBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6507618 7.92E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_015559 SETBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs8099273 6.66E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_015559 SETBP1 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Albumins rs10502868 7.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_015569 DNM3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs10914144 2.00E-14 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_015569 DNM3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs678962 3.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_015569 DNM3 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs1011731 1.00E-17 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_015570 AUTS2 21471458 http://www.ncbi.nlm.nih.gov/pubmed/21471458 Alcohol Drinking rs6943555 4.00E-08 Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption. NHGRI|-1
NM_015570 AUTS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Body Mass Index rs10263639 3.04E-05 Genomewide association analysis of body mass index (BMI) in a birth cohort from a founder population dbGaP|2896
NM_015570 AUTS2 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs10263639 3.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_015570 AUTS2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs6961611 7.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_015576 ERC2 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs1795648 6.00E-06 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_015577 RAI14 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10075914 7.33E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_015577 RAI14 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs409045 8.00E-07 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NM_015589 SAMD4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4901519 7.56E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_015630 EPC2 21123754 http://www.ncbi.nlm.nih.gov/pubmed/21123754 Alzheimer Disease rs2121433 1.00E-06 "Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort." NHGRI|-1
NM_015630 EPC2 21123754 http://www.ncbi.nlm.nih.gov/pubmed/21123754 Alzheimer Disease rs4499362 1.00E-06 "Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort." NHGRI|-1
NM_015630 EPC2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Interleukin-8 rs10191411 4.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_015634 KIAA1279 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2491015 1.76E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_015641 TES 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1464776 1.55E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_015641 TES 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12673240 8.31E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_015646 RAP1B 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Leukocyte Count rs12313946 3.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_015651 PHF19 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs1953126 4.00E-11 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_015651 PHF19 19503088 http://www.ncbi.nlm.nih.gov/pubmed/19503088 "Arthritis, Rheumatoid" rs881375 4.00E-08 "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis." NHGRI|-1
NM_015653 RIBC2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11913200 7.08E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_015656 KIF26A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4983568 8.02E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_015657 ABCA12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs3795857 5.80E-06 NBL-GWAS version 2 dbGaP|2895
NM_015657 ABCA12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs11677798 2.38E-06 NBL-GWAS version 2 dbGaP|2895
NM_015657 ABCA12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2592232 8.87E-10 NBL-GWAS version 2 dbGaP|2895
NM_015657 ABCA12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10498025 5.45E-11 NBL-GWAS version 2 dbGaP|2895
NM_015657 ABCA12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10498026 9.69E-09 NBL-GWAS version 2 dbGaP|2895
NM_015657 ABCA12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1952224 1.77E-05 NBL-GWAS version 2 dbGaP|2895
NM_015677 SH3YL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10181051 5.38E-05 NBL-GWAS version 2 dbGaP|2895
NM_015677 SH3YL1 21423239 http://www.ncbi.nlm.nih.gov/pubmed/21423239 "Suicide, Attempted" rs300774 5.00E-08 A genome-wide association study of attempted suicide. NHGRI|-1
NM_015678 NBEA 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs1777672 4.00E-07 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_015686 FAM155B 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs4844096 5.00E-11 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_015688 FAM184B 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs7678436 8.00E-15 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_015689 DENND2A 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs10237118 4.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_015692 CPAMD8 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs11666377 7.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_015693 INTU 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs12639834 6.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_015693 INTU 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs950063 9.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_015693 INTU 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Ankle Brachial Index rs1320267 7.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_015702 MMADHC 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs11889862 2.00E-06 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_015702 MMADHC 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs6716455 7.00E-07 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_015702 MMADHC 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs6716455 9.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_015718 NOX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9322522 1.42E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_015718 NOX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7754577 2.73E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_015718 NOX3 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs35229355 5.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_015718 NOX3 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11759141 9.21E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_015718 NOX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9480303 1.47E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_015718 NOX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9397922 5.74E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_015831 ACHE 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs7636 5.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_015832 MBD2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs1039189 4.33E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_015833 ADARB1 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Respiratory Function Tests rs2838815 3.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_015834 ADARB1 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Respiratory Function Tests rs2838815 3.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_015848 KRT76 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7397684 2.09E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_015866 PRDM2 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs2245218 2.13E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_015869 PPARG 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1801282 2.00E-06 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_015869 PPARG 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs1801282 2.00E-06 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_015869 PPARG 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs1801282 2.00E-06 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_015869 PPARG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs9833097 6.72E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_015874 RBPJ 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs10517086 5.00E-10 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_015874 RBPJ 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs874040 1.00E-16 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_015879 ST8SIA3 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs1120787 7.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_015895 GMNN 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs17419851 9.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_015905 TRIM24 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Weight rs1874326 9.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_015908 SRRT 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs12666989 2.00E-08 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_015909 NBAS 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs7581919 8.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_015909 NBAS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs7581919 7.44E-04 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_015910 C2orf86 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Interleukin-6 rs11683229 6.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_015915 ATL1 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs17122693 3.00E-07 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_015932 POMP 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs9550386 4.89E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_015945 SLC35C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs12480667 1.90E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_015957 APIP 21602797 http://www.ncbi.nlm.nih.gov/pubmed/21602797 Cystic Fibrosis rs12793173 1.00E-09 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. NHGRI|-1
NM_015958 DPH5 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs17410015 2.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_015960 CUTC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17112202 8.74E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_015967 PTPN22 17804836 http://www.ncbi.nlm.nih.gov/pubmed/17804836 "Arthritis, Rheumatoid" rs2476601 2.00E-11 TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. NHGRI|-1
NM_015967 PTPN22 19503088 http://www.ncbi.nlm.nih.gov/pubmed/19503088 "Arthritis, Rheumatoid" rs2476601 2.00E-21 "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis." NHGRI|-1
NM_015967 PTPN22 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs2476601 9.00E-74 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_015967 PTPN22 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2476601 1.00E-08 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_015967 PTPN22 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 "Diabetes Mellitus, Type 1" rs2476601 1.00E-07 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NM_015967 PTPN22 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs2476601 2.00E-80 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_015967 PTPN22 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2476601 9.00E-85 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_015967 PTPN22 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs2476601 1.00E-07 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_015972 POLR1D 21471979 http://www.ncbi.nlm.nih.gov/pubmed/21471979 "Lymphoma, Large B-Cell, Diffuse" rs7097 7.00E-06 Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility. NHGRI|-1
NM_015976 SNX7 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1351563 7.27E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_015978 TNNI3K 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs1514175 8.00E-14 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_015980 HMP19 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs10475598 8.00E-07 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_015984 UCHL5 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs9427573 5.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_015984 UCHL5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs842796 7.60E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_015984 UCHL5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs842796 8.50E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_015993 PLLP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs8044834 8.68E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_016045 SLMO2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6070706 4.79E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_016050 MRPL11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1791682 1.08E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_016053 CCDC53 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs7971536 8.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_016061 YPEL5 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs7579944 1.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_016071 MRPS33 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs528957 7.80E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_016071 MRPS33 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs557962 5.86E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_016078 FAM18B1 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs4924935 8.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_016081 PALLD 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs17054392 3.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_016081 PALLD 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs2710833 6.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_016082 CDK5RAP1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs291671 2.00E-15 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_016082 CDK5RAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs291671 2.47E-04 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_016083 CNR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs964647 2.09E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_016096 ZNF706 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs1264202 2.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_016096 ZNF706 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3491 1.79E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_016108 AIG1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6939141 1.97E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_016115 ASB3 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Hemoglobins rs1160297 1.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_016115 ASB3 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Hemoglobins rs2357013 6.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_016133 INSIG2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs13028041 1.66E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_016133 INSIG2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs651477 2.00E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_016133 INSIG2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs651477 7.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_016134 PGCP 20802479 http://www.ncbi.nlm.nih.gov/pubmed/20802479 Migraine Disorders rs1835740 2.00E-11 Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. NHGRI|-1
NM_016142 HSD17B12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4620711 6.31E-06 NBL-GWAS version 2 dbGaP|2895
NM_016142 HSD17B12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs11037575 3.87E-06 NBL-GWAS version 2 dbGaP|2895
NM_016142 HSD17B12 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs11037575 9.55E-07 NBL-GWAS version 1 dbGaP|2845
NM_016142 HSD17B12 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs11037466 2.87E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_016142 HSD17B12 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4755731 2.47E-07 NBL-GWAS version 1 dbGaP|2845
NM_016142 HSD17B12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4755731 3.87E-06 NBL-GWAS version 2 dbGaP|2895
NM_016144 COMMD10 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs7702057 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_016152 RARB 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs1435703 4.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_016152 RARB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6795607 2.36E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_016152 RARB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9819865 6.81E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_016152 RARB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10865802 1.32E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_016152 RARB 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs993804 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_016152 RARB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs993804 4.39E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_016174 CERCAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1009850 5.21E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_016179 TRPC4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs17210569 3.59E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_016180 SLC45A2 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs16891982 1.00E-12 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_016180 SLC45A2 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs16891982 4.00E-20 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_016180 SLC45A2 17999355 http://www.ncbi.nlm.nih.gov/pubmed/17999355 Skin Pigmentation rs16891982 3.00E-11 A genomewide association study of skin pigmentation in a South Asian population. NHGRI|-1
NM_016180 SLC45A2 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs35391 3.00E-10 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_016180 SLC45A2 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs28777 1.00E-17 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_016180 SLC45A2 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs28777 9.00E-14 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_016190 CRNN 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs908922 4.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_016192 TMEFF2 17903298 http://www.ncbi.nlm.nih.gov/pubmed/17903298 Diabetes Mellitus rs10497721 7.00E-07 Genome-wide association with diabetes-related traits in the Framingham Heart Study. NHGRI|-1
NM_016192 TMEFF2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs13007495 4.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_016192 TMEFF2 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs1385351 4.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_016196 RBM19 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 C-Reactive Protein rs11066587 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_016200 NAA38 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12706164 5.23E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_016200 NAA38 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7456706 8.33E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_016203 PRKAG2 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs7805747 4.00E-12 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_016203 PRKAG2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs10224002 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_016203 PRKAG2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs10224002 6.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_016203 PRKAG2 21305692 http://www.ncbi.nlm.nih.gov/pubmed/21305692 Bipolar Disorder rs7795096 2.00E-06 Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder. NHGRI|-1
NM_016205 PDGFC 19786962 http://www.ncbi.nlm.nih.gov/pubmed/19786962 Speech Perception rs4234898 5.00E-08 First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. NHGRI|-1
NM_016206 VGLL3 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs2660753 3.00E-08 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_016206 VGLL3 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs9284813 5.00E-09 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_016206 VGLL3 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs17181170 3.00E-08 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_016206 VGLL3 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs7629490 1.00E-07 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_016206 VGLL3 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7642134 4.00E-10 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_016224 SNX9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6903041 1.19E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_016227 C1orf9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2859242 6.73E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_016229 CYB5R2 19557197 http://www.ncbi.nlm.nih.gov/pubmed/19557197 Waist Circumference rs7932813 5.00E-06 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. NHGRI|-1
NM_016232 IL1RL1 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Eosinophils rs1420101 5.00E-14 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_016232 IL1RL1 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs13015714 4.00E-09 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_016235 GPRC5B 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs12444979 3.00E-21 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_016240 SCARA3 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs569214 4.00E-08 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_016242 EMCN 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Piperazines rs1405687 5.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_016247 IMPG2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs3732893 3.92E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_016260 IKZF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs16849204 3.22E-05 NBL-GWAS version 2 dbGaP|2895
NM_016260 IKZF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7600221 6.53E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_016260 IKZF2 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Eosinophils rs12619285 5.00E-10 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_016269 LEF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17038960 3.00E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_016270 KLF2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12185505 3.68E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_016279 CDH9 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs2548003 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_016279 CDH9 19404256 http://www.ncbi.nlm.nih.gov/pubmed/19404256 Autistic Disorder rs4307059 2.00E-10 Common genetic variants on 5p14.1 associate with autism spectrum disorders. NHGRI|-1
NM_016279 CDH9 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs4479806 8.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_016282 AK3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs385893 9.00E-17 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_016284 CNOT1 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs37062 1.00E-06 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_016284 CNOT1 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs37062 3.00E-25 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_016284 CNOT1 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs7188697 7.00E-25 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_016290 UIMC1 19448621 http://www.ncbi.nlm.nih.gov/pubmed/19448621 Menarche rs365132 8.00E-14 Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. NHGRI|-1
NM_016298 FBXO40 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs3772130 6.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_016302 CRBN 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4055307 1.85E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_016302 CRBN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9829721 6.83E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_016302 CRBN 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1601875 7.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_016304 RSL24D1 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs16976033 7.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_016307 PRRX2 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Astigmatism rs7866070 7.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_016321 RHCG 18193045 http://www.ncbi.nlm.nih.gov/pubmed/18193045 Body Height rs4932217 8.00E-07 Common variants in the GDF5-UQCC region are associated with variation in human height. NHGRI|-1
NM_016329 SFMBT1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2336725 1.00E-12 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_016341 PLCE1 21368711 http://www.ncbi.nlm.nih.gov/pubmed/21368711 Religion and Psychology rs9419788 4.00E-08 Genome-wide association study of personality traits in bipolar patients. NHGRI|-1
NM_016341 PLCE1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs11187837 4.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_016341 PLCE1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs3765524 2.00E-09 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_016341 PLCE1 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs117607728 4.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_016341 PLCE1 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs2274223 4.00E-20 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_016341 PLCE1 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs3781264 4.00E-09 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_016341 PLCE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs3781264 2.31E-04 Genome-wide association between genotype and incident stroke in participants of primarily self-described European ancestry dbGaP|2886
NM_016343 CENPF 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs438034 5.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_016343 CENPF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs438034 8.93E-04 Genome-wide association between genotype and incident stroke in participants of primarily self-described European ancestry dbGaP|2886
NM_016347 NAT8 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs13538 5.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_016354 SLCO4A1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs872626 5.95E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_016356 DCDC2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs793834 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_016358 IRX4 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs12653946 4.00E-18 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_016358 IRX4 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs6879627 8.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_016358 IRX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs370672 6.66E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_016363 GP6 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs1671152 8.00E-14 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_016366 CABP2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4930431 5.65E-06 NBL-GWAS version 1 dbGaP|2845
NM_016372 TPRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11915684 3.50E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_016372 TPRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4679351 1.81E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_016372 TPRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6809319 2.64E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_016372 TPRA1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs9871760 4.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_016372 TPRA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs9871760 4.12E-05 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_016373 WWOX 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs2059238 3.00E-06 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_016373 WWOX 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs17706989 1.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_016373 WWOX 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs2859631 1.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_016373 WWOX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs8047442 2.97E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_016373 WWOX 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs9923451 8.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_016373 WWOX 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1109934 3.45E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_016373 WWOX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7200634 7.11E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_016378 VCX2 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs7892812 8.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_016378 VCX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs5934349 1.75E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_016401 C11orf73 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs6592284 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_016408 CDK5RAP1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs291671 2.00E-15 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_016408 CDK5RAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs291671 2.47E-04 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_016410 CHMP5 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs12336160 1.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_016417 GLRX5 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs8005962 8.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_016434 RTEL1 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs6010620 2.00E-09 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_016434 RTEL1 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs6010620 3.00E-12 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_016434 RTEL1 19578366 http://www.ncbi.nlm.nih.gov/pubmed/19578366 Glioma rs6010620 3.00E-09 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. NHGRI|-1
NM_016434 RTEL1 19578366 http://www.ncbi.nlm.nih.gov/pubmed/19578366 Glioma rs4809324 2.00E-09 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. NHGRI|-1
NM_016434 RTEL1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2297441 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_016441 CRIM1 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs7562790 8.00E-09 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_016441 CRIM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs884215 2.34E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_016442 ERAP1 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs27524 3.00E-11 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_016442 ERAP1 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Aminopeptidases rs13160562 7.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_016442 ERAP1 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs30187 2.00E-27 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_016442 ERAP1 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs27434 5.00E-12 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_016447 MPP6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2529059 3.32E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_016457 PRKD2 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs11083846 4.00E-09 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NM_016457 PRKD2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs425105 3.00E-11 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_016470 C20orf111 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognition rs6017291 6.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_016478 ZC3HC1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs11556924 9.00E-18 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_016485 VTA1 21060863 http://www.ncbi.nlm.nih.gov/pubmed/21060863 Retinal Vein rs225717 1.00E-16 "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo." NHGRI|-1
NM_016495 TBC1D7 17903304 http://www.ncbi.nlm.nih.gov/pubmed/17903304 Cardiovascular Diseases rs499818 7.00E-06 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. NHGRI|-1
NM_016500 CXorf26 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs5937496 6.00E-07 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_016522 NTM 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs1550976 3.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_016522 NTM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs1550976 5.59E-06 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_016522 NTM 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs992564 4.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_016524 SYT17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6497337 2.12E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_016526 BET1L 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs11602954 1.00E-14 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_016526 BET1L 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs2280543 4.00E-12 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_016527 HAO2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs868675 6.28E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_016527 HAO2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1341797 6.95E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_016531 KLF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6838905 6.46E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_016531 KLF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6838905 7.66E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_016531 KLF3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7658334 1.49E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_016533 NINJ2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2535436 9.93E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_016533 NINJ2 19369658 http://www.ncbi.nlm.nih.gov/pubmed/19369658 Stroke rs12425791 1.00E-09 Genomewide association studies of stroke. NHGRI|-1
NM_016544 DNAJC27 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs4665736 7.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_016544 DNAJC27 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs713586 6.00E-22 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_016559 PEX5L 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs7630877 7.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_016569 TBX3 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs1896312 3.00E-17 Genome-wide association study of PR interval. NHGRI|-1
NM_016569 TBX3 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs2384550 4.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_016569 TBX3 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs10850409 3.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_016569 TBX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10492258 6.91E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_016569 TBX3 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Tyrosine rs2194980 3.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_016569 TBX3 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs35444 1.00E-10 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_016569 TBX3 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs35444 8.00E-07 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_016569 TBX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs35444 7.12E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_016569 TBX3 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs11067228 2.00E-11 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_016574 DRD2 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Atrial Natriuretic Factor rs1079596 3.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_016574 DRD2 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11214606 5.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_016586 MBIP 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs1168987 5.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_016586 MBIP 19198613 http://www.ncbi.nlm.nih.gov/pubmed/19198613 Thyroid Neoplasms rs944289 2.00E-09 Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. NHGRI|-1
NM_016589 C3orf1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs2293370 3.00E-11 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_016592 GNAS 21046636 http://www.ncbi.nlm.nih.gov/pubmed/21046636 Brain Waves rs13831 6.00E-06 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. NHGRI|-1
NM_016601 KCNK9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4556079 4.79E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_016601 KCNK9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11781101 5.31E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_016601 KCNK9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7004938 2.97E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_016601 KCNK9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11783351 5.51E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_016601 KCNK9 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4736239 7.42E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_016601 KCNK9 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs13270196 2.27E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_016601 KCNK9 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs994770 2.78E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_016601 KCNK9 21700879 http://www.ncbi.nlm.nih.gov/pubmed/21700879 Adiponectin rs2468677 8.00E-07 Novel Locus FER Is Associated With Serum HMW Adiponectin Levels. NHGRI|-1
NM_016604 KDM3B 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs757647 5.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_016612 SLC25A37 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11776817 1.66E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_016612 SLC25A37 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs1512268 3.00E-30 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_016612 SLC25A37 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs1512268 4.00E-11 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_016615 SLC6A13 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Creatinine rs10774021 1.00E-09 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_016616 TXNDC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2722292 5.10E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_016618 KRCC1 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs12714207 5.00E-07 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_016621 PHF21A 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs16938437 6.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_016621 PHF21A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11038830 1.81E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7624303 6.79E-05 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs9857883 7.19E-05 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1193510 9.86E-05 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs9827781 1.95E-05 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6441188 7.47E-06 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10936131 8.61E-05 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6778370 7.84E-06 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7639867 8.50E-06 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs939114 1.66E-05 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs11716327 9.71E-05 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7632059 7.21E-06 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10936142 1.06E-05 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6441201 3.43E-07 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2885663 4.77E-06 NBL-GWAS version 2 dbGaP|2895
NM_016625 RSRC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1714518 5.71E-07 NBL-GWAS version 2 dbGaP|2895
NM_016640 MRPS30 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs7716600 7.00E-07 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_016640 MRPS30 20686651 http://www.ncbi.nlm.nih.gov/pubmed/20686651 Cornea rs10941694 9.00E-06 Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases. NHGRI|-1
NM_016640 MRPS30 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs4415084 8.00E-11 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_016644 PRR16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10463741 8.47E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_016651 DACT1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10150529 1.49E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_016653 ZAK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs10187560 8.98E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_016733 LIMK2 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic Nephropathies rs2106294 4.00E-06 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_016815 GYPC 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs13418717 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_016815 GYPC 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6710520 2.18E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_016815 GYPC 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10207651 7.81E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_016818 ABCG1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Personality rs425215 8.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_016824 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7090030 7.39E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_016824 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11194995 7.62E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_016824 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11194996 7.62E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_016824 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11195001 7.19E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_016824 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7917994 8.56E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_016824 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7921757 8.56E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_016824 ADD3 20460270 http://www.ncbi.nlm.nih.gov/pubmed/20460270 Biliary Atresia rs17095355 7.00E-09 Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. NHGRI|-1
NM_016830 VAMP1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10492096 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_016831 PER3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs2797685 7.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_016834 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17563986 3.44E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_016834 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs242557 9.00E-18 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_016834 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1981997 2.02E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_016834 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs8070723 3.36E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_016834 MAPT 21044948 http://www.ncbi.nlm.nih.gov/pubmed/21044948 Parkinson Disease rs8070723 7.00E-12 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. NHGRI|-1
NM_016834 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs8070723 2.00E-118 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_016835 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17563986 3.44E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_016835 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs242557 9.00E-18 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_016835 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1981997 2.02E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_016835 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs8070723 3.36E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_016835 MAPT 21044948 http://www.ncbi.nlm.nih.gov/pubmed/21044948 Parkinson Disease rs8070723 7.00E-12 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. NHGRI|-1
NM_016835 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs8070723 2.00E-118 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_016836 RBMS1 20418489 http://www.ncbi.nlm.nih.gov/pubmed/20418489 "Diabetes Mellitus, Type 2" rs7593730 4.00E-08 Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. NHGRI|-1
NM_016836 RBMS1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs10192369 9.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_016836 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6432628 9.13E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_016836 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13034284 1.85E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_016836 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9967749 8.13E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_016836 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11681327 4.77E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_016836 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7603576 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_016836 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2551691 9.03E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_016836 RBMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs197275 4.42E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_016841 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17563986 3.44E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_016841 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs242557 9.00E-18 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_016841 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1981997 2.02E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_016841 MAPT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs8070723 3.36E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_016841 MAPT 21044948 http://www.ncbi.nlm.nih.gov/pubmed/21044948 Parkinson Disease rs8070723 7.00E-12 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. NHGRI|-1
NM_016841 MAPT 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs8070723 2.00E-118 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_016848 SHC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13295927 6.31E-06 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_016848 SHC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13294002 7.20E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_016929 CLIC5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4714860 7.86E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_016930 STX18 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7679624 7.00E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_016931 NOX4 20801717 http://www.ncbi.nlm.nih.gov/pubmed/20801717 Amyotrophic Lateral Sclerosis rs1488902 3.00E-06 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. NHGRI|-1
NM_016950 SPOCK3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7657608 2.65E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_016954 TBX22 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1474563 3.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_017410 HOXC13 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs1443512 6.00E-16 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_017410 HOXC13 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs7969151 2.00E-06 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_017410 HOXC13 20460270 http://www.ncbi.nlm.nih.gov/pubmed/20460270 Biliary Atresia rs2120991 9.00E-06 Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. NHGRI|-1
NM_017416 IL1RAPL2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs210432 7.56E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_017425 SPA17 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs12807809 2.00E-09 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_017429 BCMO1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Interleukin-1beta rs4889294 5.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_017429 BCMO1 19185284 http://www.ncbi.nlm.nih.gov/pubmed/19185284 beta Carotene rs6564851 2.00E-24 "Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study." NHGRI|-1
NM_017431 PRKAG3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9973579 9.29E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_017434 DUOX1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7169193 3.89E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_017434 DUOX1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1648312 3.44E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_017435 SLCO1C1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs10770705 8.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_017437 CPSF2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs1009170 2.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_017437 CPSF2 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs12896399 1.00E-16 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_017437 CPSF2 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs12896399 2.00E-23 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_017437 CPSF2 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Eye Color rs12896399 4.00E-38 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_017437 CPSF2 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Hair Color rs12896399 1.00E-48 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_017437 CPSF2 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12896399 5.00E-13 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_017437 CPSF2 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs12896399 8.00E-21 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_017440 MDM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs10492304 1.68E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_017446 MRPL39 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs17001239 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_017459 MFAP2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2284746 4.00E-29 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_017491 WDR1 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs717615 5.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_017495 RBM38 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs6092477 1.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_017495 RBM38 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs6070116 4.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_017508 SOX6 19714249 http://www.ncbi.nlm.nih.gov/pubmed/19714249 Obesity rs297325 4.00E-07 Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males. NHGRI|-1
NM_017508 SOX6 19714249 http://www.ncbi.nlm.nih.gov/pubmed/19714249 Obesity rs4756846 5.00E-07 Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males. NHGRI|-1
NM_017508 SOX6 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7117858 6.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_017508 SOX6 21104366 http://www.ncbi.nlm.nih.gov/pubmed/21104366 Bone Density rs11023787 5.00E-16 A genome-wide association analysis implicates SOX6 as a candidate gene for wrist bone mass. NHGRI|-1
NM_017509 KLK15 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs266849 6.00E-10 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_017516 RAB39 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10890784 1.84E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_017519 ARID1B 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs9478751 3.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_017519 ARID1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6917698 2.61E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_017519 ARID1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs288944 3.28E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_017519 ARID1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs288945 5.18E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_017519 ARID1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2817460 1.40E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_017519 ARID1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1246182 1.54E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_017522 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs5177 5.00E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_017522 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11206127 3.16E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_017522 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs869987 4.54E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_017522 LRP8 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs114216682 7.00E-08 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_017522 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17785382 1.74E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_017525 CDC42BPG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs670358 7.71E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_017525 CDC42BPG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs670358 3.27E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_017526 LEPROT 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs1892534 7.00E-21 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_017526 LEPROT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs1892534 4.77E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_017526 LEPROT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs2889195 5.95E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_017526 LEPROT 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4420065 4.00E-62 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_017526 LEPROT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs4420065 6.67E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_017526 LEPROT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Inflammation rs12753193 3.76E-07 Genomewide association analysis of inflammation (CRP) in a birth cohort from a founder population dbGaP|2897
NM_017526 LEPROT 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Inflammation rs12753193 4.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_017544 NKRF 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2018358 6.49E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_017549 EPDR1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1524058 1.00E-09 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_017551 GRID1 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs7910620 7.00E-07 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_017551 GRID1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs12767486 7.37E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_017575 SMG6 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs1231206 9.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_017575 SMG6 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs216172 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_017575 SMG6 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs10852932 2.00E-11 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_017579 DMBT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7902878 9.49E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_017583 TRIM44 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Nonalcoholic Fatty Liver Disease rs7928794 8.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_017585 SLC2A6 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2073935 6.05E-08 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_017586 C9orf7 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs4962153 8.00E-21 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_017586 C9orf7 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs4962153 8.05E-14 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_017586 C9orf7 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs739468 2.79E-14 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_017586 C9orf7 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs3094379 2.93E-13 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_017594 DIRAS2 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs1831521 8.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_017594 DIRAS2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs10821091 9.39E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_017594 DIRAS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7858079 4.34E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_017594 DIRAS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10821402 4.43E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_017596 KIF21B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10494828 5.13E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_017596 KIF21B 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs2297909 5.00E-12 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_017596 KIF21B 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs11584383 2.00E-07 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_017596 KIF21B 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs11584383 1.00E-11 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_017622 C17orf59 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs8531 1.91E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_017623 CNNM3 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs9948 6.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_017625 ITLN1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2274910 1.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_017628 TET2 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs10005603 7.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_017628 TET2 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs7679673 3.00E-14 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_017633 FAM46A 21606135 http://www.ncbi.nlm.nih.gov/pubmed/21606135 Coronary Artery Disease rs16893526 5.00E-06 A Genome-wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease. NHGRI|-1
NM_017637 BNC2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7860932 2.90E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_017637 BNC2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10810632 3.76E-07 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_017637 BNC2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10756815 4.61E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_017637 BNC2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6475082 7.45E-07 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_017637 BNC2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4961760 7.13E-07 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_017637 BNC2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2254193 1.12E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_017637 BNC2 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Melanosis rs2153271 4.00E-10 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_017637 BNC2 19648919 http://www.ncbi.nlm.nih.gov/pubmed/19648919 Ovarian Neoplasms rs3814113 5.00E-19 A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. NHGRI|-1
NM_017637 BNC2 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Mass Index rs1927702 6.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_017639 DCHS2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs12649437 2.20E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_017640 LRRC16A 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Iron rs2274089 5.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_017640 LRRC16A 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs2274089 3.00E-07 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_017640 LRRC16A 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs2274089 8.00E-07 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_017640 LRRC16A 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs742132 9.00E-09 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_017640 LRRC16A 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs932316 9.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_017649 CNNM2 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs12413409 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_017649 CNNM2 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Disease rs12413409 4.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_017649 CNNM2 20364137 http://www.ncbi.nlm.nih.gov/pubmed/20364137 Intracranial Aneurysm rs12413409 1.00E-09 Genome-wide association study of intracranial aneurysm identifies three new risk loci. NHGRI|-1
NM_017653 DYM 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs8099594 3.00E-07 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_017659 QPCTL 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2287019 2.00E-16 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_017661 ZNF280D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7175191 1.64E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_017662 TRPM6 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs11144134 8.00E-15 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_017677 MTMR8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6524881 4.80E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_017677 MTMR8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs5964778 4.80E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_017679 BCAS3 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs8068952 3.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_017679 BCAS3 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Creatinine rs9895661 1.00E-15 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_017684 VPS13C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4143844 4.93E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_017684 VPS13C 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs17271305 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_017684 VPS13C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs3934516 5.53E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_017700 ARHGEF38 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Liver Cirrhosis rs7669317 8.00E-08 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_017705 PAQR5 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11072089 3.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_017712 PGPEP1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs7248363 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_017712 PGPEP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7248363 3.85E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_017714 TASP1 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs1223271 5.00E-06 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_017719 SNRK 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs17075286 8.00E-07 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_017734 PALMD 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs7543130 1.00E-07 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_017737 FNBP1L 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs237438 5.24E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_017737 FNBP1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs237425 9.56E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_017740 ZDHHC7 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs2326458 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_017741 DCAF16 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs7678436 8.00E-15 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_017753 LPPR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2417226 8.20E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_017755 NSUN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs563624 6.12E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_017757 ZNF407 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7245160 4.22E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_017759 INO80D 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs7603514 8.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_017763 RNF43 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs2257205 8.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_017766 CASZ1 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs880315 3.00E-10 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_017766 CASZ1 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs880315 7.00E-07 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_017766 CASZ1 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs12046278 5.00E-06 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_017766 CASZ1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1280975 4.93E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_017771 PXK 18204446 http://www.ncbi.nlm.nih.gov/pubmed/18204446 "Lupus Erythematosus, Systemic" rs6445975 7.00E-09 "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci." NHGRI|-1
NM_017774 CDKAL1 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs9295474 9.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_017774 CDKAL1 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs4712523 2.00E-12 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_017774 CDKAL1 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs4712523 7.00E-20 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_017774 CDKAL1 18711366 http://www.ncbi.nlm.nih.gov/pubmed/18711366 "Diabetes Mellitus, Type 2" rs4712524 3.00E-10 SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations. NHGRI|-1
NM_017774 CDKAL1 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs10946398 1.00E-08 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_017774 CDKAL1 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs10946398 7.00E-07 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_017774 CDKAL1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7754840 4.00E-11 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_017774 CDKAL1 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs7754840 4.00E-11 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_017774 CDKAL1 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs7756992 8.00E-09 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_017774 CDKAL1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs10440833 2.00E-22 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_017774 CDKAL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs2206734 5.05E-04 Genome-wide association between genotype and incident myocardial infarction in African-American participants dbGaP|2883
NM_017774 CDKAL1 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs6931514 1.00E-11 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_017774 CDKAL1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs9465871 3.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_017774 CDKAL1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs6908425 9.00E-10 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_017784 OSBPL10 20610895 http://www.ncbi.nlm.nih.gov/pubmed/20610895 Vascular Diseases rs1902341 5.00E-07 Identification of evidence suggestive of an association with peripheral arterial disease at the OSBPL10 locus by genome-wide investigation in the Japanese population. NHGRI|-1
NM_017784 OSBPL10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs936160 1.94E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_017785 CCDC99 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs13156607 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_017797 BTBD2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3810414 5.70E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_017797 BTBD2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2074625 4.29E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_017805 RASIP1 21060863 http://www.ncbi.nlm.nih.gov/pubmed/21060863 Retinal Vein rs2287921 2.00E-25 "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo." NHGRI|-1
NM_017814 TMEM161A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs964132 7.26E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_017814 TMEM161A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11669988 6.75E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_017816 LYAR 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2920228 2.92E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_017816 LYAR 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2920228 3.32E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_017822 C12orf41 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7315319 5.84E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_017824 5-Mar 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11186926 3.40E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_017824 5-Mar 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1057848 5.80E-06 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_017824 5-Mar 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11186960 8.74E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_017831 RNF125 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7226543 4.30E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_017867 C4orf27 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4692758 9.61E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_017869 BANP 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs4843747 2.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_017869 BANP 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs12447690 6.00E-22 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_017869 BANP 20485516 http://www.ncbi.nlm.nih.gov/pubmed/20485516 Cornea rs12447690 9.00E-11 Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. NHGRI|-1
NM_017886 ULK4 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs9815354 3.00E-09 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_017890 VPS13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4735627 2.26E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_017891 C1orf159 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Mass Index rs3934834 6.00E-07 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_017895 DDX27 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1079661 1.42E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_017898 MOSC2 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Cornea rs1494373 6.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_017898 MOSC2 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Amyotrophic Lateral Sclerosis rs337161 3.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_017902 HIF1AN 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs4509693 6.00E-06 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_017915 C12orf48 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs2292303 8.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_017919 STX17 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs10760706 4.00E-07 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_017921 NPLOC4 20463881 http://www.ncbi.nlm.nih.gov/pubmed/20463881 Eye Color rs9894429 9.00E-14 Digital quantification of human eye color highlights genetic association of three new loci. NHGRI|-1
NM_017923 1-Mar 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs3792615 9.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_017926 C14orf118 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs2121070 5.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_017926 C14orf118 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Attention Deficit Disorder with Hyperactivity rs2360997 8.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_017926 C14orf118 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs935334 3.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_017929 PEX26 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs462904 3.01E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_017933 PID1 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs6436839 3.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_017935 BANK1 18204447 http://www.ncbi.nlm.nih.gov/pubmed/18204447 "Lupus Erythematosus, Systemic" rs10516487 4.00E-10 Functional variants in the B-cell gene BANK1 are associated with systemic lupus erythematosus. NHGRI|-1
NM_017935 BANK1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7694392 4.26E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_017935 BANK1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4640677 6.62E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_017935 BANK1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs12648641 9.89E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_017945 SLC35A5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs766968 2.64E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_017949 CUEDC1 20802204 http://www.ncbi.nlm.nih.gov/pubmed/20802204 Multiple Sclerosis rs8074980 2.00E-06 Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. NHGRI|-1
NM_017952 PTCD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1075622 1.59E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_017952 PTCD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2367202 2.09E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_017952 PTCD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1025104 1.60E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_017954 CADPS2 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs2429582 6.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_017970 C14orf102 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2282032 1.19E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_017970 C14orf102 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs2282032 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_017972 C14orf118 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs2121070 5.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_017972 C14orf118 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Attention Deficit Disorder with Hyperactivity rs2360997 8.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_017972 C14orf118 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs935334 3.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_017974 ATG16L1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs10210302 5.00E-14 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_017974 ATG16L1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs3828309 2.00E-32 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_017974 ATG16L1 17435756 http://www.ncbi.nlm.nih.gov/pubmed/17435756 Crohn Disease rs2241880 1.00E-13 Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. NHGRI|-1
NM_017974 ATG16L1 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs2241880 3.00E-06 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_017974 ATG16L1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2241880 4.40E-08 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_017974 ATG16L1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs3792109 7.00E-41 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_017974 ATG16L1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs3792106 2.31E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_017974 ATG16L1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs10933436 7.00E-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_017991 KIAA1310 21046636 http://www.ncbi.nlm.nih.gov/pubmed/21046636 Brain Waves rs4907240 4.00E-06 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. NHGRI|-1
NM_017993 ENOX1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs1324015 9.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_018000 MREG 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs7590720 1.00E-08 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_018000 MREG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1250255 3.21E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_018003 UACA 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs6494849 7.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_018011 ARGLU1 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs1927745 5.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_018012 KIF26B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1538472 4.54E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_018012 KIF26B 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs10924270 3.00E-10 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_018014 BCL11A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7593947 8.46E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_018014 BCL11A 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs1427407 6.00E-31 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_018014 BCL11A 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs766432 1.00E-10 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_018014 BCL11A 18245381 http://www.ncbi.nlm.nih.gov/pubmed/18245381 Fetal Hemoglobin rs11886868 7.00E-35 Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. NHGRI|-1
NM_018014 BCL11A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7592415 1.56E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_018014 BCL11A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17552189 8.46E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_018014 BCL11A 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs17552189 4.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_018014 BCL11A 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs991964 9.00E-06 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_018014 BCL11A 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs887912 2.00E-12 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_018014 BCL11A 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs10490113 5.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_018014 BCL11A 21493818 http://www.ncbi.nlm.nih.gov/pubmed/21493818 Monocyte early outgrowth colony forming units rs6712720 4.00E-06 Genetic and clinical correlates of early-outgrowth colony-forming units. NHGRI|-1
NM_018014 BCL11A 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs10202231 7.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_018014 BCL11A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs243023 1.13E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_018014 BCL11A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs243023 5.95E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_018014 BCL11A 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs243021 3.00E-15 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_018014 BCL11A 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs2540917 1.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_018027 FRMD4A 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs1541010 1.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_018027 FRMD4A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7901829 8.05E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_018030 OSBPL1A 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Sex Hormone-Binding Globulin rs9635963 2.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_018030 OSBPL1A 20548944 http://www.ncbi.nlm.nih.gov/pubmed/20548944 Osteoporosis rs7227401 4.00E-07 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. NHGRI|-1
NM_018035 ATP5SL 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs17318596 5.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_018040 GPATCH2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs1497828 4.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_018051 WDR60 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs2730245 3.00E-07 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_018057 SLC6A15 20662065 http://www.ncbi.nlm.nih.gov/pubmed/20662065 Lupus Vulgaris rs2403106 3.00E-06 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. NHGRI|-1
NM_018057 SLC6A15 21521612 http://www.ncbi.nlm.nih.gov/pubmed/21521612 "Depressive Disorder, Major" rs1545843 1.00E-09 The neuronal transporter gene SLC6A15 confers risk to major depression. NHGRI|-1
NM_018057 SLC6A15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2125716 1.13E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_018058 CRTAC1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs531676 9.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_018058 CRTAC1 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs508001 7.00E-09 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_018062 FANCL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs848291 3.41E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_018063 HELLS 19578179 http://www.ncbi.nlm.nih.gov/pubmed/19578179 Acenocoumarol rs12772169 8.00E-12 A genome-wide association study of acenocoumarol maintenance dosage. NHGRI|-1
NM_018063 HELLS 19706858 http://www.ncbi.nlm.nih.gov/pubmed/19706858 Ticlopidine rs12777823 2.00E-13 Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy. NHGRI|-1
NM_018079 SRBD1 20363506 http://www.ncbi.nlm.nih.gov/pubmed/20363506 Cardiovascular Diseases rs3213787 3.00E-09 Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility. NHGRI|-1
NM_018079 SRBD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12622230 4.02E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_018080 VPS13C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4143844 4.93E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_018080 VPS13C 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs17271305 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_018080 VPS13C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs3934516 5.53E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_018082 POLR3B 21084426 http://www.ncbi.nlm.nih.gov/pubmed/21084426 Parkinson Disease rs4964469 2.00E-07 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. NHGRI|-1
NM_018082 POLR3B 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs3891355 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_018086 FIGN 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10189532 3.39E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_018086 FIGN 21572416 http://www.ncbi.nlm.nih.gov/pubmed/21572416 Blood Pressure rs16849225 4.00E-11 Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. NHGRI|-1
NM_018086 FIGN 19680635 http://www.ncbi.nlm.nih.gov/pubmed/19680635 "Parkinson Disease, Secondary" rs12476047 3.00E-06 Genome-wide association study of antipsychotic-induced parkinsonism severity among schizophrenia patients. NHGRI|-1
NM_018088 FAM90A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12830720 6.93E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_018091 ELP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4732838 4.66E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_018099 FAR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs10843215 1.52E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_018099 FAR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs16933618 3.44E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_018103 LRRC8D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1215582 8.52E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_018115 SDAD1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs2273 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_018116 MSTO1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs602905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_018117 WDR11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7068008 1.76E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_018117 WDR11 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7071661 2.27E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_018122 DARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6691327 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_018126 TMEM33 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs16853571 5.59E-07 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_018127 ELAC2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3944086 6.41E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_018130 SHQ1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10049211 5.35E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_018130 SHQ1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11128275 3.80E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_018130 SHQ1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6775777 2.36E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_018136 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12677 3.65E-09 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_018136 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12677 5.97E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_018136 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12034362 4.45E-14 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_018136 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12034362 7.46E-13 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_018136 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2026429 6.24E-11 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_018136 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2026429 7.66E-12 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_018136 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4915337 3.65E-09 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_018136 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4915337 5.97E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_018136 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1888991 3.65E-09 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_018136 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1888991 5.97E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_018136 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6677082 3.99E-09 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_018136 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6677082 4.57E-09 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_018136 ASPM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6677082 6.47E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_018137 PRMT6 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs12726652 5.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_018137 PRMT6 19754311 http://www.ncbi.nlm.nih.gov/pubmed/19754311 Acquired Immunodeficiency Syndrome rs4118325 6.00E-07 Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). NHGRI|-1
NM_018140 CEP72 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs4957048 1.00E-09 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_018140 CEP72 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs11739663 3.00E-08 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_018142 INTS10 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs7816032 2.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_018142 INTS10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6983139 2.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_018142 INTS10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6983139 5.10E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_018153 ANTXR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6710260 2.53E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_018159 NUDT11 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs5945619 2.00E-09 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_018159 NUDT11 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs1327301 2.00E-10 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_018159 NUDT11 18264098 http://www.ncbi.nlm.nih.gov/pubmed/18264098 Prostatic Neoplasms rs5945572 4.00E-13 Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. NHGRI|-1
NM_018161 NADSYN1 20541252 http://www.ncbi.nlm.nih.gov/pubmed/20541252 Vitamin D rs12785878 2.00E-27 Common genetic determinants of vitamin D insufficiency: a genome-wide association study. NHGRI|-1
NM_018165 PBRM1 20081856 http://www.ncbi.nlm.nih.gov/pubmed/20081856 Mood Disorders rs2251219 2.00E-09 Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. NHGRI|-1
NM_018179 ATF7IP 20543847 http://www.ncbi.nlm.nih.gov/pubmed/20543847 Testicular Neoplasms rs2900333 6.00E-10 "Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer." NHGRI|-1
NM_018181 ZNF532 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs937815 1.88E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_018181 ZNF532 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17761525 7.05E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_018183 SBNO1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs11830103 4.00E-15 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_018184 ARL8B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2616521 3.49E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_018192 LEPREL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs16865151 1.71E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_018192 LEPREL1 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs16865258 2.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_018192 LEPREL1 18794855 http://www.ncbi.nlm.nih.gov/pubmed/18794855 Urinary Bladder Neoplasms rs710521 1.00E-07 Sequence variant on 8q24 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_018192 LEPREL1 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs710521 2.00E-10 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_018192 LEPREL1 20348956 http://www.ncbi.nlm.nih.gov/pubmed/20348956 Urinary Bladder Neoplasms rs710521 6.00E-08 A sequence variant at 4p16.3 confers susceptibility to urinary bladder cancer. NHGRI|-1
NM_018197 ZFP64 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs6013382 5.00E-06 Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_018197 ZFP64 19478329 http://www.ncbi.nlm.nih.gov/pubmed/19478329 "Infertility, Male" rs6068020 5.00E-07 Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. NHGRI|-1
NM_018199 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 2.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_018199 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_018200 HMG20A 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs7119 5.00E-07 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_018202 TMEM57 21700265 http://www.ncbi.nlm.nih.gov/pubmed/21700265 Blood Sedimentation rs10903129 5.00E-13 Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. NHGRI|-1
NM_018202 TMEM57 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs10903129 5.00E-10 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_018208 ETNK2 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs3795578 7.00E-06 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_018217 EDEM2 20802025 http://www.ncbi.nlm.nih.gov/pubmed/20802025 Protein C rs6120849 7.00E-37 Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. NHGRI|-1
NM_018218 USP40 21646302 http://www.ncbi.nlm.nih.gov/pubmed/21646302 Bilirubin rs6704644 8.00E-08 Mayo genome consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. NHGRI|-1
NM_018222 PARVA 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs7120489 7.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_018225 SMU1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10813928 1.45E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_018226 RNPEPL1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Bipolar Disorder rs2953145 7.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_018238 AGK 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs528957 7.80E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_018238 AGK 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs557962 5.86E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_018240 KIRREL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12123554 5.48E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_018240 KIRREL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1925035 1.49E-05 NBL-GWAS version 2 dbGaP|2895
NM_018244 UQCC 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs6060369 1.00E-16 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_018244 UQCC 18193045 http://www.ncbi.nlm.nih.gov/pubmed/18193045 Body Height rs6060369 2.00E-16 Common variants in the GDF5-UQCC region are associated with variation in human height. NHGRI|-1
NM_018244 UQCC 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs6088792 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_018244 UQCC 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs6060373 2.00E-17 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_018244 UQCC 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs6088813 1.00E-13 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_018248 NEIL3 17903306 http://www.ncbi.nlm.nih.gov/pubmed/17903306 Heart Rate rs1395479 7.00E-06 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. NHGRI|-1
NM_018249 CDK5RAP2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4642724 3.93E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_018249 CDK5RAP2 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs16909449 1.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_018249 CDK5RAP2 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Cornea rs4837752 6.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_018253 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs651905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_018253 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs602905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_018256 WDR12 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs6725887 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_018256 WDR12 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs6725887 1.00E-08 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_018259 TTC17 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs11037466 2.87E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_018259 TTC17 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4755731 2.47E-07 NBL-GWAS version 1 dbGaP|2845
NM_018259 TTC17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4755731 3.87E-06 NBL-GWAS version 2 dbGaP|2895
NM_018261 EXOC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4333263 1.12E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_018261 EXOC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs13120644 6.72E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_018264 TYW1B 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6460033 1.16E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_018264 TYW1B 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6460033 2.84E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_018264 TYW1B 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs6460033 1.72E-07 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_018265 C1orf106 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs7554511 1.00E-06 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_018265 C1orf106 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs7554511 2.00E-13 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_018268 WDR41 21502949 http://www.ncbi.nlm.nih.gov/pubmed/21502949 Caudate Nucleus rs163030 2.00E-07 Discovery and replication of dopamine-related gene effects on caudate volume in young and elderly populations (N=1198) using genome-wide search. NHGRI|-1
NM_018287 ARHGAP12 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs7081678 6.00E-06 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_018291 FGGY 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 "Diabetes Mellitus, Type 2" rs17119280 7.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_018291 FGGY 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs12727131 3.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_018291 FGGY 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs4601609 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_018294 CWF19L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2270962 4.61E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_018302 C4orf19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6830100 1.86E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_018303 EXOC2 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs6918152 5.00E-07 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_018303 EXOC2 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs6918152 6.00E-08 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_018303 EXOC2 21131588 http://www.ncbi.nlm.nih.gov/pubmed/21131588 "Leukemia, Lymphoid" rs9378805 2.00E-06 Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL. NHGRI|-1
NM_018303 EXOC2 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Melanosis rs1540771 4.00E-18 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_018303 EXOC2 21700618 http://www.ncbi.nlm.nih.gov/pubmed/21700618 "Carcinoma, Basal Cell" rs12210050 1.00E-09 Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma. NHGRI|-1
NM_018303 EXOC2 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs12210050 5.00E-14 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_018313 PBRM1 20081856 http://www.ncbi.nlm.nih.gov/pubmed/20081856 Mood Disorders rs2251219 2.00E-09 Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. NHGRI|-1
NM_018315 FBXW7 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs360929 9.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_018318 CCDC91 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2638953 7.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_018318 CCDC91 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs522958 1.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_018318 CCDC91 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs522958 8.00E-07 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_018325 C9orf72 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs774359 3.00E-06 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_018325 C9orf72 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs12555345 5.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_018325 C9orf72 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs7029145 9.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_018325 C9orf72 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs10812610 3.47E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_018325 C9orf72 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs10812610 5.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_018325 C9orf72 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs2814707 7.00E-09 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_018325 C9orf72 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs3849942 1.00E-08 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_018325 C9orf72 20801718 http://www.ncbi.nlm.nih.gov/pubmed/20801718 Amyotrophic Lateral Sclerosis rs3849942 9.00E-11 Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. NHGRI|-1
NM_018327 SPTLC3 21368711 http://www.ncbi.nlm.nih.gov/pubmed/21368711 Personality rs17190927 8.00E-07 Genome-wide association study of personality traits in bipolar patients. NHGRI|-1
NM_018327 SPTLC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6109595 1.47E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_018327 SPTLC3 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs2073233 1.00E-06 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_018327 SPTLC3 19798445 http://www.ncbi.nlm.nih.gov/pubmed/19798445 Ceramides rs680379 8.00E-15 Genetic determinants of circulating sphingolipid concentrations in European populations. NHGRI|-1
NM_018330 KIAA1598 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs7078160 2.00E-08 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_018349 MCTP2 19483685 http://www.ncbi.nlm.nih.gov/pubmed/19483685 Drug-Induced Liver Injury rs4984390 4.00E-06 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. NHGRI|-1
NM_018349 MCTP2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs1014922 3.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_018349 MCTP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2199724 2.59E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_018349 MCTP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2046006 9.03E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_018349 MCTP2 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Alkaline Phosphatase rs7173947 3.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_018349 MCTP2 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs933769 7.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_018349 MCTP2 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs4321143 7.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_018356 C5orf22 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4867365 1.62E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_018356 C5orf22 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs16901423 1.23E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_018361 AGPAT5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17637986 5.17E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_018361 AGPAT5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17637986 5.45E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_018361 AGPAT5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2912091 3.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_018361 AGPAT5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2912089 3.72E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_018363 RNLS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2162361 4.54E-06 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_018363 RNLS 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs10509540 1.00E-28 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_018364 RSBN1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Arthritis, Rheumatoid" rs6679677 6.00E-25 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_018364 RSBN1 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 "Arthritis, Rheumatoid" rs6679677 6.00E-42 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_018364 RSBN1 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs6679677 1.00E-40 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_018364 RSBN1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs6679677 5.00E-26 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_018364 RSBN1 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs6679677 8.00E-24 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_018366 CNO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4626203 7.83E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_018368 LMBRD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2094596 1.83E-05 NBL-GWAS version 2 dbGaP|2895
NM_018371 CSGALNACT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6983139 2.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_018371 CSGALNACT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6983139 5.10E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_018372 C1orf103 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1282020 8.95E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_018372 C1orf103 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1282023 8.95E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_018372 C1orf103 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1548342 8.72E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_018401 STK32B 19389651 http://www.ncbi.nlm.nih.gov/pubmed/19389651 Electrocardiography rs2008242 3.00E-06 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. NHGRI|-1
NM_018402 IL26 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs2870946 5.00E-07 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_018404 ADAP2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs3760318 2.00E-09 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_018405 C17orf79 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs315437 1.71E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_018410 HJURP 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs579327 7.00E-08 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_018413 CHST11 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs12811699 8.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_018418 SPATA7 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs17124581 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_018421 TBC1D2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs16914086 5.60E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_018431 DOK5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7274170 8.42E-06 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_018431 DOK5 20215924 http://www.ncbi.nlm.nih.gov/pubmed/20215924 Amygdala rs2023454 5.00E-07 A genome-wide association study of amygdala activation in youths with and without bipolar disorder. NHGRI|-1
NM_018434 RNF130 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs13161895 6.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_018437 HEMGN 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Thyrotropin rs755109 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_018437 HEMGN 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs4743150 5.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_018441 PECR 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs7590720 1.00E-08 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_018460 ARHGAP15 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Weight rs10928195 4.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_018482 ASAP1 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs6984045 2.00E-06 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_018482 ASAP1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Fructose-Bisphosphate Aldolase rs10092658 6.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_018484 SLC22A11 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs17300741 7.00E-14 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_018484 SLC22A11 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs2078267 1.00E-06 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_018484 SLC22A11 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs2078267 2.00E-26 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_018488 TBX4 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs2079795 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_018488 TBX4 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs757608 6.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_018530 GSDMB 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs2305480 1.00E-07 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_018530 GSDMB 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs2305480 3.00E-08 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_018530 GSDMB 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2290400 6.00E-13 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_018530 GSDMB 17611496 http://www.ncbi.nlm.nih.gov/pubmed/17611496 Asthma rs7216389 9.00E-11 Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. NHGRI|-1
NM_018530 GSDMB 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs2872507 9.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_018530 GSDMB 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2872507 5.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_018530 GSDMB 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2872507 5.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_018530 GSDMB 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs8067378 1.00E-07 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_018534 NRP2 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs7603514 8.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_018556 SIRPG 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2281808 1.00E-11 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_018557 LRP1B 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Optic Nerve rs491391 3.00E-07 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_018557 LRP1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs9287300 3.43E-05 NBL-GWAS version 2 dbGaP|2895
NM_018557 LRP1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6735489 2.27E-05 NBL-GWAS version 2 dbGaP|2895
NM_018557 LRP1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs13432282 5.13E-05 NBL-GWAS version 2 dbGaP|2895
NM_018557 LRP1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs13420111 3.90E-05 NBL-GWAS version 2 dbGaP|2895
NM_018557 LRP1B 19367585 http://www.ncbi.nlm.nih.gov/pubmed/19367585 Aging rs12474609 6.00E-09 A genome screen of successful aging without cognitive decline identifies LRP1B by haplotype analysis. NHGRI|-1
NM_018557 LRP1B 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs10210358 2.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_018557 LRP1B 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12476507 7.29E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_018557 LRP1B 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs12472911 2.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_018559 KIAA1704 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7336303 7.84E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_018566 YOD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2054780 4.60E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_018602 DNAJA4 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Exploratory Behavior rs1533665 7.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_018647 TNFRSF19 20512145 http://www.ncbi.nlm.nih.gov/pubmed/20512145 Nasopharyngeal Neoplasms rs9510787 2.00E-09 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. NHGRI|-1
NM_018647 TNFRSF19 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs753955 2.00E-12 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_018647 TNFRSF19 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9507108 2.60E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_018647 TNFRSF19 20512145 http://www.ncbi.nlm.nih.gov/pubmed/20512145 Nasopharyngeal Neoplasms rs1572072 1.00E-08 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. NHGRI|-1
NM_018654 GPRC5D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1056927 7.24E-05 NBL-GWAS version 2 dbGaP|2895
NM_018654 GPRC5D 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs704225 6.66E-06 NBL-GWAS version 1 dbGaP|2845
NM_018657 MYNN 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs10936599 5.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_018657 MYNN 20972440 http://www.ncbi.nlm.nih.gov/pubmed/20972440 Colorectal Neoplasms rs10936599 3.00E-08 "Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33." NHGRI|-1
NM_018659 CYTL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4566595 7.88E-06 NBL-GWAS version 2 dbGaP|2895
NM_018659 CYTL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6446700 7.63E-05 NBL-GWAS version 2 dbGaP|2895
NM_018659 CYTL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4234840 4.56E-06 NBL-GWAS version 2 dbGaP|2895
NM_018659 CYTL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs13139027 1.75E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_018659 CYTL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4689963 8.76E-07 NBL-GWAS version 2 dbGaP|2895
NM_018662 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NM_018662 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_018662 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_018662 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_018668 VPS33B 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Sphingomyelins rs886144 2.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_018672 ABCA5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs558076 2.53E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_018672 ABCA5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs817097 6.22E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_018683 RNF114 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2235617 4.20E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_018683 RNF114 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6125829 5.86E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_018684 ZC4H2 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs7064929 7.00E-07 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_018684 ZC4H2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7890561 8.45E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_018686 CMAS 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs10743430 6.00E-07 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_018689 KIAA1199 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12593088 7.11E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_018696 ELAC1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9807334 6.28E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_018699 PRDM5 17903298 http://www.ncbi.nlm.nih.gov/pubmed/17903298 Blood Glucose rs180730 5.00E-06 Genome-wide association with diabetes-related traits in the Framingham Heart Study. NHGRI|-1
NM_018699 PRDM5 17903298 http://www.ncbi.nlm.nih.gov/pubmed/17903298 Blood Glucose rs180730 6.00E-06 Genome-wide association with diabetes-related traits in the Framingham Heart Study. NHGRI|-1
NM_018699 PRDM5 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs343166 4.74E-06 NBL-GWAS version 1 dbGaP|2845
NM_018699 PRDM5 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs10017284 6.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018702 ADARB2 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs11250464 6.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_018702 ADARB2 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs2999399 6.00E-06 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_018702 ADARB2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Fat Distribution rs6560749 8.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_018702 ADARB2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Mass Index rs6560749 2.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_018703 RBBP6 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs11643520 6.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_018710 TMEM55A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7846412 1.14E-07 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_018710 TMEM55A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7846412 4.55E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_018712 ELMOD1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Personality rs10431058 8.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_018719 CDCA7L 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs1175000 5.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_018719 CDCA7L 17903292 http://www.ncbi.nlm.nih.gov/pubmed/17903292 Thyrotropin rs10499559 8.00E-06 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_018719 CDCA7L 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs13227860 1.26E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_018723 RBFOX1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs6500744 3.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_018723 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13336322 9.10E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_018723 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7188257 7.46E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_018723 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4786850 3.70E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_018723 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17822719 2.54E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_018723 RBFOX1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit Disorder with Hyperactivity rs12921846 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_018723 RBFOX1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1551960 4.67E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_018723 RBFOX1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs899305 6.31E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_018723 RBFOX1 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Nonalcoholic Fatty Liver Disease rs9302841 2.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_018723 RBFOX1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs4787008 6.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_018723 RBFOX1 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Phosphatidylcholines rs9924951 5.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs16870907 2.46E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241453 3.04E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241452 2.07E-72 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241448 7.86E-70 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241447 4.69E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241440 2.36E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1015166 8.68E-107 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241427 3.48E-82 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_018833 TAP2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs241427 1.66E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241425 1.60E-94 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs241424 7.96E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1894406 9.40E-88 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2857106 2.39E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9784758 6.79E-77 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_018833 TAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9784758 2.30E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_018836 AJAP1 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Height rs7513590 5.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_018836 AJAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4400585 1.58E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_018836 AJAP1 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Factor VII rs966321 8.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_018836 AJAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6679220 1.00E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_018836 AJAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4654432 7.20E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_018836 AJAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4654433 9.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_018837 SULF2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4810663 1.93E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_018837 SULF2 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs4810685 7.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_018837 SULF2 20173747 http://www.ncbi.nlm.nih.gov/pubmed/20173747 Atrial Fibrillation rs13038095 2.00E-07 Common variants in KCNN3 are associated with lone atrial fibrillation. NHGRI|-1
NM_018844 BCAP29 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs10953541 3.00E-08 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_018844 BCAP29 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs10953541 9.98E-05 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_018891 LAMC2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs1028771 4.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_018891 LAMC2 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs525410 6.00E-07 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_018897 DNAH7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs16841387 4.84E-06 NBL-GWAS version 2 dbGaP|2895
NM_018897 DNAH7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs186895 4.24E-05 NBL-GWAS version 2 dbGaP|2895
NM_018897 DNAH7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs341933 6.00E-06 NBL-GWAS version 2 dbGaP|2895
NM_018897 DNAH7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1489802 9.35E-05 NBL-GWAS version 2 dbGaP|2895
NM_018897 DNAH7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs16842717 7.79E-05 NBL-GWAS version 2 dbGaP|2895
NM_018897 DNAH7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6719500 2.39E-05 NBL-GWAS version 2 dbGaP|2895
NM_018945 PDE7B 20558539 http://www.ncbi.nlm.nih.gov/pubmed/20558539 Phosphorus rs947583 3.00E-12 Common genetic variants associate with serum phosphorus concentration. NHGRI|-1
NM_018945 PDE7B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs947583 8.88E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_018948 ERRFI1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs12727642 9.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_018950 HLA-F 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1362126 7.54E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_018959 DAZAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7251833 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_018961 UBASH3A 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs11203203 4.00E-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_018961 UBASH3A 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs11203203 1.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_018961 UBASH3A 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs11203203 2.00E-09 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_018961 UBASH3A 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs11203203 1.00E-09 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_018961 UBASH3A 18840781 http://www.ncbi.nlm.nih.gov/pubmed/18840781 "Diabetes Mellitus, Type 1" rs9976767 2.00E-08 Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes. NHGRI|-1
NM_018967 SNTG1 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Respiratory Function Tests rs310558 5.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_018967 SNTG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2046355 3.39E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_018968 SNTG2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4971342 6.81E-06 NBL-GWAS version 1 dbGaP|2845
NM_018970 GPR85 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 acylcarnitine rs10953730 2.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_018970 GPR85 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10229603 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_018972 GDAP1 17903300 http://www.ncbi.nlm.nih.gov/pubmed/17903300 Waist Circumference rs4471028 2.00E-07 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. NHGRI|-1
NM_018972 GDAP1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Myoglobin rs6472866 8.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_018975 TERF2IP 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs1948632 8.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_018979 WNK1 19369658 http://www.ncbi.nlm.nih.gov/pubmed/19369658 Stroke rs12425791 1.00E-09 Genomewide association studies of stroke. NHGRI|-1
NM_018988 GFOD1 17903304 http://www.ncbi.nlm.nih.gov/pubmed/17903304 Cardiovascular Diseases rs499818 7.00E-06 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. NHGRI|-1
NM_018993 RIN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6046396 5.09E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_018993 RIN2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs6046396 4.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_019000 FAM134B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs26015 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_019000 FAM134B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs16868670 2.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_019002 ETAA1 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs724568 5.00E-06 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_019006 ZFAND6 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs11634397 2.00E-09 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_019010 KRT20 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs2315504 8.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_019021 C11orf71 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs2847476 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_019021 C11orf71 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2852438 5.77E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_019022 TMX3 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs13353224 9.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_019022 TMX3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1704734 8.69E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_019023 PRMT7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs8058517 4.37E-08 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_019023 PRMT7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs8058517 8.82E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_019023 PRMT7 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs7197653 2.00E-06 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_019024 HEATR5B 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs17020136 2.00E-09 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_019026 TMCO1 21532571 http://www.ncbi.nlm.nih.gov/pubmed/21532571 "Glaucoma, Open-Angle" rs4656461 6.00E-14 Genome-wide association study identifies susceptibility loci for open angle glaucoma at TMCO1 and CDKN2B-AS1. NHGRI|-1
NM_019029 CPVL 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs2252521 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_019029 CPVL 17903298 http://www.ncbi.nlm.nih.gov/pubmed/17903298 "Hemoglobin A, Glycosylated" rs10486607 8.00E-06 Genome-wide association with diabetes-related traits in the Framingham Heart Study. NHGRI|-1
NM_019035 PCDH18 19165918 http://www.ncbi.nlm.nih.gov/pubmed/19165918 "Lupus Erythematosus, Systemic" rs2313132 8.00E-06 Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. NHGRI|-1
NM_019035 PCDH18 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs2313982 1.85E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_019035 PCDH18 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1519337 3.54E-05 NBL-GWAS version 2 dbGaP|2895
NM_019043 APBB1IP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10508719 1.40E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_019046 ANKRD16 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2380205 5.00E-07 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_019052 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs1265086 2.69E-11 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_019052 CCHCR1 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 "Colitis, Ulcerative" rs9263739 4.00E-67 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_019052 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11967883 3.15E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_019052 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs1265078 2.04E-21 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_019052 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs17196989 3.96E-10 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_019052 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9263749 5.60E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_019052 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111962041 4.16E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_019052 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113481038 8.56E-14 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_019052 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3130453 2.06E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_019052 CCHCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3094187 3.73E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_019053 EXOC6 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs1111875 3.00E-06 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_019053 EXOC6 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1111875 6.00E-10 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_019053 EXOC6 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs1111875 6.00E-10 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_019053 EXOC6 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs1111875 7.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_019053 EXOC6 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs5015480 1.00E-15 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_019053 EXOC6 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs5015480 5.00E-06 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_019053 EXOC6 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs5015480 7.00E-08 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_019053 EXOC6 20862305 http://www.ncbi.nlm.nih.gov/pubmed/20862305 "Diabetes Mellitus, Type 2" rs5015480 9.00E-06 Identification of new genetic risk variants for type 2 diabetes. NHGRI|-1
NM_019053 EXOC6 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs2497306 5.00E-09 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_019060 CRCT1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair rs499697 1.00E-10 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_019062 RNF186 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs1317209 2.00E-10 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_019062 RNF186 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs3806308 7.00E-09 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_019062 RNF186 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs6426833 2.00E-11 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_019062 RNF186 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs6426833 2.00E-21 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_019062 RNF186 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6426833 4.00E-35 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_019062 RNF186 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs6426833 5.00E-13 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_019075 UGT1A10 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs11892031 1.00E-07 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_019075 UGT1A10 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs2602381 4.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_019075 UGT1A10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1604144 4.75E-05 NBL-GWAS version 2 dbGaP|2895
NM_019075 UGT1A10 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs887829 1.00E-69 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_019075 UGT1A10 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs6742078 5E-324 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_019075 UGT1A10 21646302 http://www.ncbi.nlm.nih.gov/pubmed/21646302 Bilirubin rs4148325 5.00E-62 Mayo genome consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. NHGRI|-1
NM_019076 UGT1A8 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs11892031 1.00E-07 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_019076 UGT1A8 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs2602381 4.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_019076 UGT1A8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1604144 4.75E-05 NBL-GWAS version 2 dbGaP|2895
NM_019076 UGT1A8 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs887829 1.00E-69 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_019076 UGT1A8 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs6742078 5E-324 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_019076 UGT1A8 21646302 http://www.ncbi.nlm.nih.gov/pubmed/21646302 Bilirubin rs4148325 5.00E-62 Mayo genome consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. NHGRI|-1
NM_019077 UGT1A7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1604144 4.75E-05 NBL-GWAS version 2 dbGaP|2895
NM_019077 UGT1A7 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs887829 1.00E-69 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_019077 UGT1A7 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs6742078 5E-324 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_019077 UGT1A7 21646302 http://www.ncbi.nlm.nih.gov/pubmed/21646302 Bilirubin rs4148325 5.00E-62 Mayo genome consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. NHGRI|-1
NM_019078 UGT1A5 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs887829 1.00E-69 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_019078 UGT1A5 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs6742078 5E-324 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_019078 UGT1A5 21646302 http://www.ncbi.nlm.nih.gov/pubmed/21646302 Bilirubin rs4148325 5.00E-62 Mayo genome consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. NHGRI|-1
NM_019080 NDFIP2 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs2039553 7.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_019080 NDFIP2 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs9574565 3.00E-07 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_019080 NDFIP2 20862305 http://www.ncbi.nlm.nih.gov/pubmed/20862305 "Diabetes Mellitus, Type 2" rs1359790 6.00E-09 Identification of new genetic risk variants for type 2 diabetes. NHGRI|-1
NM_019083 CCDC76 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6681721 2.47E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_019083 CCDC76 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs12733952 4.78E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_019086 VSIG10 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs4767658 4.09E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_019087 ARL15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs271243 1.33E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_019087 ARL15 20011104 http://www.ncbi.nlm.nih.gov/pubmed/20011104 Adiponectin rs4311394 3.00E-08 A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. NHGRI|-1
NM_019087 ARL15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs37539 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_019090 KIAA1383 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4308924 7.97E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_019093 UGT1A3 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs887829 1.00E-69 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_019093 UGT1A3 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs6742078 5E-324 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_019093 UGT1A3 21646302 http://www.ncbi.nlm.nih.gov/pubmed/21646302 Bilirubin rs4148325 5.00E-62 Mayo genome consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. NHGRI|-1
NM_019094 NUDT4 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1836127 3.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_019105 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2077580 7.45E-32 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_019105 TNXB 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs12198173 3.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_019105 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12198173 8.39E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_019105 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs204878 1.21E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_019105 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs17201560 1.56E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_019105 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs17201560 8.14E-09 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_019105 TNXB 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs185819 3.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_019105 TNXB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130287 2.26E-28 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019105 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1150754 1.96E-106 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019105 TNXB 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1150754 6.66E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019105 TNXB 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs1150754 6.00E-29 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_019105 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1150752 3.64E-86 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019105 TNXB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs17421624 1.79E-08 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019105 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1269854 1.08E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_019105 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1269854 7.53E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_019105 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3134954 1.40E-108 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019105 TNXB 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Eosinophils rs2269426 3.00E-06 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_019110 ZKSCAN4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs9380069 1.38E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_019110 ZKSCAN4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs967005 3.38E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3129871 1.15E-299 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs3129871 1.75E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019111 HLA-DRA 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs9268645 1.00E-100 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_019111 HLA-DRA 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9268645 9.21E-10 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3129882 1.39E-178 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019111 HLA-DRA 20711177 http://www.ncbi.nlm.nih.gov/pubmed/20711177 Parkinson Disease rs3129882 2.00E-10 Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. NHGRI|-1
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2239804 1.89E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_019111 HLA-DRA 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs7192 2.02E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7192 5.43E-10 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_019111 HLA-DRA 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs7194 6.01E-25 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019111 HLA-DRA 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs3135388 4.00E-225 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_019111 HLA-DRA 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3135388 9.00E-81 Risk alleles for multiple sclerosis identified by a genomewide study. NHGRI|-1
NM_019111 HLA-DRA 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Leukocyte Count rs2227139 1.00E-07 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_019111 HLA-DRA 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3129890 1.62E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs6937545 4.29E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs7754768 1.21E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs7763262 4.29E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3129962 5.23E-98 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019111 HLA-DRA 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3129962 5.60E-18 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3129963 6.53E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_019111 HLA-DRA 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3129963 7.92E-14 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9268528 3.12E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019111 HLA-DRA 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9268530 3.21E-14 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9268542 3.12E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs3135377 4.30E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_019111 HLA-DRA 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3135377 6.32E-28 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019111 HLA-DRA 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2395162 7.69E-14 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019111 HLA-DRA 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9268557 7.37E-17 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019111 HLA-DRA 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9268560 1.83E-16 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3135353 1.15E-84 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3135353 1.43E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_019111 HLA-DRA 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3135353 5.17E-17 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9268585 9.27E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9268589 1.45E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019111 HLA-DRA 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs7756262 3.49E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9501624 2.36E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7762370 5.13E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9501626 1.39E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3129860 8.62E-192 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3135338 1.59E-280 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs3135338 1.31E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019111 HLA-DRA 20159113 http://www.ncbi.nlm.nih.gov/pubmed/20159113 Multiple Sclerosis rs3135338 2.00E-25 Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. NHGRI|-1
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2027856 1.11E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9268615 1.46E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2395173 1.19E-281 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019111 HLA-DRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2395173 1.31E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019112 ABCA7 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs3764650 5.00E-17 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_019112 ABCA7 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs3752246 6.00E-07 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_019117 KLHL4 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs2710057 1.00E-06 New sequence variants associated with bone mineral density. NHGRI|-1
NM_019555 ARHGEF3 19110211 http://www.ncbi.nlm.nih.gov/pubmed/19110211 Platelet Count rs12485738 4.00E-27 A genome-wide association study identifies three loci associated with mean platelet volume. NHGRI|-1
NM_019555 ARHGEF3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs12485738 6.00E-31 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_019555 ARHGEF3 21452313 http://www.ncbi.nlm.nih.gov/pubmed/21452313 "Arthritis, Rheumatoid" rs2062583 2.00E-06 Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci. NHGRI|-1
NM_019558 HOXD8 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs2592394 5.00E-07 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_019590 KIAA1217 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 "Ear, External" rs11013962 3.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_019590 KIAA1217 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11014058 6.43E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_019595 ITSN2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2543662 5.11E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_019595 ITSN2 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs6707600 3.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_019599 TAS2R1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6884905 9.18E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_019599 TAS2R1 19812673 http://www.ncbi.nlm.nih.gov/pubmed/19812673 Autistic Disorder rs10513025 3.00E-07 A genome-wide linkage and association scan reveals novel loci for autism. NHGRI|-1
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1980493 4.90E-69 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019602 BTNL2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1980493 2.22E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019602 BTNL2 19287509 http://www.ncbi.nlm.nih.gov/pubmed/19287509 "Peptides, Cyclic" rs1980493 5.00E-07 Genome-wide association study of determinants of anti-cyclic citrullinated peptide antibody titer in adults with rheumatoid arthritis. NHGRI|-1
NM_019602 BTNL2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2076533 2.36E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019602 BTNL2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2076530 2.49E-10 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019602 BTNL2 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 "Colitis, Ulcerative" rs9268480 3.00E-06 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_019602 BTNL2 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs2076529 4.00E-07 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_019602 BTNL2 20305777 http://www.ncbi.nlm.nih.gov/pubmed/20305777 "Osteoarthritis, Knee" rs10947262 5.00E-09 New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study. NHGRI|-1
NM_019602 BTNL2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3806156 4.56E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019602 BTNL2 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs3806156 7.00E-19 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_019602 BTNL2 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs3763313 2.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3129962 5.23E-98 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019602 BTNL2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3129962 5.60E-18 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3129963 6.53E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_019602 BTNL2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3129963 7.92E-14 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9268528 3.12E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019602 BTNL2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9268530 3.21E-14 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9268542 3.12E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs3135377 4.30E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_019602 BTNL2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3135377 6.32E-28 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019602 BTNL2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2395162 7.69E-14 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019602 BTNL2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9268557 7.37E-17 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019602 BTNL2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9268560 1.83E-16 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3135353 1.15E-84 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3135353 1.43E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_019602 BTNL2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3135353 5.17E-17 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9268585 9.27E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9268589 1.45E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019602 BTNL2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs7756262 3.49E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9501624 2.36E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs7762370 5.13E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9501626 1.39E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3129860 8.62E-192 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3135338 1.59E-280 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs3135338 1.31E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019602 BTNL2 20159113 http://www.ncbi.nlm.nih.gov/pubmed/20159113 Multiple Sclerosis rs3135338 2.00E-25 Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. NHGRI|-1
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2027856 1.11E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9268615 1.46E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2395173 1.19E-281 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2395173 1.31E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs3117106 8.77E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_019602 BTNL2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9268429 4.55E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_019602 BTNL2 21326295 http://www.ncbi.nlm.nih.gov/pubmed/21326295 Vitiligo rs7758128 8.00E-11 Genome-wide analysis identifies a quantitative trait locus in the MHC class II region associated with generalized vitiligo age of onset. NHGRI|-1
NM_019602 BTNL2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs4424066 7.40E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_019602 BTNL2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3117099 6.29E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_019602 BTNL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3117098 1.69E-106 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_019602 BTNL2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs3817973 7.10E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_019616 F7 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Factor VII rs561241 5.00E-16 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_019617 GKN1 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs4254535 5.00E-06 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_019619 PARD3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs563507 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_019619 PARD3 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs7905537 8.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_019619 PARD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1780436 2.41E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_019619 PARD3 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1780436 3.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_019624 ABCB9 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs7296418 2.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_019625 ABCB9 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs7296418 2.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_019644 ANKRD7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs41943 1.61E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_019844 SLCO1B3 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs2117032 3.00E-14 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_019849 SLC7A10 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory Bowel Diseases rs10500264 4.00E-10 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_019849 SLC7A10 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs736289 9.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_019859 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs699213 9.06E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_019859 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12259754 3.59E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_019859 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11186286 3.84E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_019859 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11186286 7.40E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_019859 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11817364 6.36E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_019860 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs699213 9.06E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_019860 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12259754 3.59E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_019860 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11186286 3.84E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_019860 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11186286 7.40E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_019860 HTR7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11817364 6.36E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_019888 MC3R 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6069551 9.25E-05 NBL-GWAS version 2 dbGaP|2895
NM_019888 MC3R 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6024619 4.54E-05 NBL-GWAS version 2 dbGaP|2895
NM_019903 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7090030 7.39E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_019903 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11194995 7.62E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_019903 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11194996 7.62E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_019903 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11195001 7.19E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_019903 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7917994 8.56E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_019903 ADD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7921757 8.56E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_019903 ADD3 20460270 http://www.ncbi.nlm.nih.gov/pubmed/20460270 Biliary Atresia rs17095355 7.00E-09 Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. NHGRI|-1
NM_020041 SLC2A9 18759275 http://www.ncbi.nlm.nih.gov/pubmed/18759275 Uric Acid rs16890979 1.00E-11 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. NHGRI|-1
NM_020041 SLC2A9 18834626 http://www.ncbi.nlm.nih.gov/pubmed/18834626 Uric Acid rs16890979 7.00E-168 Association of three genetic loci with uric acid concentration and risk of gout: a genome-wide association study. NHGRI|-1
NM_020041 SLC2A9 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs734553 1.00E-192 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_020041 SLC2A9 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs734553 1.00E-41 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_020041 SLC2A9 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Gout rs13129697 4.00E-13 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_020041 SLC2A9 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Uric Acid rs13129697 1.00E-09 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_020041 SLC2A9 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Uric Acid rs13129697 2.00E-242 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_020041 SLC2A9 18327257 http://www.ncbi.nlm.nih.gov/pubmed/18327257 Uric Acid rs737267 3.00E-09 "SLC2A9 is a newly identified urate transporter influencing serum urate concentration, urate excretion and gout." NHGRI|-1
NM_020041 SLC2A9 17997608 http://www.ncbi.nlm.nih.gov/pubmed/17997608 Uric Acid rs6855911 2.00E-16 The GLUT9 gene is associated with serum uric acid levels in Sardinia and Chianti cohorts. NHGRI|-1
NM_020041 SLC2A9 18179892 http://www.ncbi.nlm.nih.gov/pubmed/18179892 Uric Acid rs7442295 2.00E-15 Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. NHGRI|-1
NM_020041 SLC2A9 18327256 http://www.ncbi.nlm.nih.gov/pubmed/18327256 Uric Acid rs7442295 3.00E-70 SLC2A9 influences uric acid concentrations with pronounced sex-specific effects. NHGRI|-1
NM_020041 SLC2A9 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs3775948 1.00E-09 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2227127 4.79E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9276429 5.39E-15 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9276431 3.40E-15 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9276432 4.28E-15 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9276435 1.36E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9276440 6.34E-15 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs10807113 7.00E-112 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10807113 2.18E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9274689 6.50E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9274741 4.72E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9274759 7.24E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs28891406 1.62E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs17212090 7.46E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9275141 2.61E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs9275141 7.42E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2856695 7.66E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs17212420 1.11E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4538747 6.53E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs7774434 3.00E-26 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_020056 HLA-DQA2 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs7774434 4.00E-34 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_020056 HLA-DQA2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs9469220 2.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9469220 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9469220 4.45E-18 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2157051 1.32E-252 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9275224 2.32E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9275224 4.45E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9275245 2.28E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs5000634 7.40E-12 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs3129720 4.91E-11 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 18668548 http://www.ncbi.nlm.nih.gov/pubmed/18668548 "Arthritis, Rheumatoid" rs6457617 1.00E-09 Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility. NHGRI|-1
NM_020056 HLA-DQA2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Arthritis, Rheumatoid" rs6457617 5.00E-75 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs6457617 1.31E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs6457617 3.61E-12 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6457617 9.47E-15 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 20383147 http://www.ncbi.nlm.nih.gov/pubmed/20383147 "Scleroderma, Systemic" rs6457617 4.00E-17 Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. NHGRI|-1
NM_020056 HLA-DQA2 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs6457617 2.00E-37 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_020056 HLA-DQA2 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 "Arthritis, Rheumatoid" rs6457620 4.00E-186 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6457620 3.41E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2647012 3.97E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2647012 1.27E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2647012 2.19E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_020056 HLA-DQA2 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs2647012 8.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_020056 HLA-DQA2 21533074 http://www.ncbi.nlm.nih.gov/pubmed/21533074 "Lymphoma, Follicular" rs2647012 2.00E-21 GWAS of follicular lymphoma reveals allelic heterogeneity at 6p21.32 and suggests shared genetic susceptibility with diffuse large B-cell lymphoma. NHGRI|-1
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9357152 1.91E-141 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9357152 1.80E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9357152 8.42E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 20639881 http://www.ncbi.nlm.nih.gov/pubmed/20639881 "Lymphoma, Follicular" rs10484561 1.00E-29 Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. NHGRI|-1
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1794282 2.48E-103 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1794282 2.21E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1794282 4.01E-18 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2856726 5.09E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2856725 2.05E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2856725 1.11E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 "Diabetes Mellitus, Type 1" rs2647044 1.00E-16 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2647046 1.04E-20 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2647050 5.38E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2856718 5.33E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2856717 1.70E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2856717 1.03E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2858305 1.70E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2858305 7.88E-14 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 20453841 http://www.ncbi.nlm.nih.gov/pubmed/20453841 "Arthritis, Rheumatoid" rs13192471 2.00E-58 A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. NHGRI|-1
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs16898264 3.85E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs9275572 1.00E-35 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_020056 HLA-DQA2 21499248 http://www.ncbi.nlm.nih.gov/pubmed/21499248 "Carcinoma, Hepatocellular" rs9275572 6.00E-09 Genome-wide association study identifies a susceptibility locus for HCV-induced hepatocellular carcinoma. NHGRI|-1
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs9275572 1.37E-09 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9275572 6.41E-14 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9275572 1.74E-20 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs12203586 5.74E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_020056 HLA-DQA2 21452313 http://www.ncbi.nlm.nih.gov/pubmed/21452313 "Arthritis, Rheumatoid" rs7765379 5.00E-23 Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci. NHGRI|-1
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs7745656 3.18E-161 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2647087 1.87E-16 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2858333 8.55E-16 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2858331 3.49E-160 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2858331 1.99E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 "Glomerulonephritis, IGA" rs9275596 2.00E-26 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9275596 1.21E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9275596 3.33E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs9275596 6.60E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs3104405 3.47E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs12177980 5.87E-92 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9275659 1.93E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9275686 2.51E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9275765 3.30E-21 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9275772 7.53E-22 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9461799 4.85E-92 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9461799 1.59E-08 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9469240 7.88E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9275793 3.13E-21 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_020056 HLA-DQA2 20711174 http://www.ncbi.nlm.nih.gov/pubmed/20711174 Narcolepsy rs2858884 3.00E-08 Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy. NHGRI|-1
NM_020056 HLA-DQA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs13199787 2.51E-96 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_020063 BARHL2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1766167 5.59E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_020063 BARHL2 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs2136093 4.00E-07 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_020063 BARHL2 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Atherosclerosis rs2390582 1.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_020063 BARHL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12116456 8.28E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_020063 BARHL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17131133 5.10E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_020063 BARHL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12133004 2.75E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_020066 FMN2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1891231 4.86E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_020066 FMN2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Coronary Disease rs17672135 2.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_020070 IGLL1 21448238 http://www.ncbi.nlm.nih.gov/pubmed/21448238 Migraine without Aura rs140174 8.00E-06 Meta-analysis of genome-wide association for migraine in six population-based European cohorts. NHGRI|-1
NM_020070 IGLL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs6519442 1.55E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_020070 IGLL1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6519442 1.49E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_020116 FSTL5 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs17638464 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_020116 FSTL5 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs6840361 4.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_020116 FSTL5 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs4470583 4.00E-07 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_020124 IFNK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs10812610 3.47E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_020124 IFNK 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs10812610 5.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_020124 IFNK 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs2814707 7.00E-09 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_020124 IFNK 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs3849942 1.00E-08 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_020124 IFNK 20801718 http://www.ncbi.nlm.nih.gov/pubmed/20801718 Amyotrophic Lateral Sclerosis rs3849942 9.00E-11 Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. NHGRI|-1
NM_020128 MDM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs10492304 1.68E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_020130 C8orf4 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs11786458 9.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_020133 AGPAT4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs729986 2.27E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_020140 ANKS1B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7968606 3.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_020140 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs2373011 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_020140 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs2373011 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_020140 ANKS1B 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11110077 4.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_020156 C1GALT1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs10259085 4.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_020156 C1GALT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10486156 3.69E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020156 C1GALT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2881814 4.90E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_020156 C1GALT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6955140 4.99E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_020157 OTOR 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs852069 3.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_020159 SMARCAD1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11097407 4.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_020159 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11097407 2.46E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020159 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2664871 2.59E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020159 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2632401 1.74E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020159 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2087170 3.46E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020159 SMARCAD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12646184 1.96E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020164 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900493 6.94E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_020164 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483170 5.79E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_020164 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483172 6.77E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_020166 MCCC1 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs10513789 3.00E-10 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_020166 MCCC1 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs11711441 8.00E-12 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_020167 NMUR2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs154104 3.78E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_020167 NMUR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4958525 8.46E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_020167 NMUR2 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs1010254 8.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_020171 GPR108 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs171094 1.39E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_020178 CA10 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs8073783 8.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_020178 CA10 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs9635759 7.00E-13 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_020180 CELF4 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs4799915 3.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_020180 CELF4 19359265 http://www.ncbi.nlm.nih.gov/pubmed/19359265 Telomere rs2162440 3.00E-06 A genome-wide association study identifies a novel locus on chromosome 18q12.2 influencing white cell telomere length. NHGRI|-1
NM_020182 PMEPA1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1334109 9.09E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_020184 CNNM4 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs2314398 3.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_020185 DUSP22 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1033180 6.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_020190 OLFML3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11810241 3.55E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_020191 MRPS22 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10513061 7.10E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_020193 C11orf30 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2155219 5.00E-16 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_020193 C11orf30 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs7927894 1.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_020193 C11orf30 19349984 http://www.ncbi.nlm.nih.gov/pubmed/19349984 "Dermatitis, Atopic" rs7927894 8.00E-10 A common variant on chromosome 11q13 is associated with atopic dermatitis. NHGRI|-1
NM_020197 SMYD2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1795030 9.30E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_020199 C5orf15 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs1644305 8.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_020203 MEPE 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1471403 2.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_020203 MEPE 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1471403 8.00E-07 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_020208 SLC6A20 21572414 http://www.ncbi.nlm.nih.gov/pubmed/21572414 Metabolism rs17279437 3.00E-19 A genome-wide association study of metabolic traits in human urine. NHGRI|-1
NM_020212 WDR93 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs17816376 2.03E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_020216 RNPEP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2819358 1.39E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_020226 PRDM8 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs16998073 1.00E-21 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_020229 PRDM11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7121790 1.34E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_020232 PSMG2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs2542151 2.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_020232 PSMG2 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs2542151 3.00E-08 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_020232 PSMG2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2542151 5.00E-17 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_020232 PSMG2 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs2542151 1.00E-14 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_020232 PSMG2 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs2542151 9.00E-08 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_020235 BBX 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs6437740 2.00E-07 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_020235 BBX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7610766 7.23E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_020235 BBX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1850344 4.72E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_020235 BBX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10511260 3.41E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_020245 TULP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs705936 4.15E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_020245 TULP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6920842 3.36E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_020246 SLC12A9 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs314370 6.00E-10 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_020246 SLC12A9 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7801190 3.00E-08 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_020297 ABCC9 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs10743430 6.00E-07 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_020298 ABCC9 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs10743430 6.00E-07 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_020307 CCNL1 20372150 http://www.ncbi.nlm.nih.gov/pubmed/20372150 Birth Weight rs900400 2.00E-35 Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. NHGRI|-1
NM_020307 CCNL1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs13064954 7.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_020317 C1orf63 21700265 http://www.ncbi.nlm.nih.gov/pubmed/21700265 Blood Sedimentation rs1043879 2.00E-09 Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. NHGRI|-1
NM_020317 C1orf63 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs1043879 1.34E-04 Genome-wide association between genotype and incident myocardial infarction in African-American participants dbGaP|2883
NM_020335 VANGL2 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs16832015 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_020337 ANKRD50 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs1986655 2.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_020338 ZMIZ1 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs704010 4.00E-09 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_020338 ZMIZ1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs703972 1.72E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_020338 ZMIZ1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs703965 8.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_020338 ZMIZ1 20526339 http://www.ncbi.nlm.nih.gov/pubmed/20526339 Vitiligo rs11593576 8.00E-07 Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. NHGRI|-1
NM_020338 ZMIZ1 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs1250540 2.00E-06 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_020338 ZMIZ1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1250552 9.00E-10 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_020338 ZMIZ1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs1250550 1.00E-30 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_020338 ZMIZ1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1250550 5.95E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_020338 ZMIZ1 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory Bowel Diseases rs1250550 6.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_020338 ZMIZ1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1916400 1.80E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_020338 ZMIZ1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs2395528 6.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_020338 ZMIZ1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs35648 3.27E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020341 PAK7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2423422 8.96E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_020342 SLC39A10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1561451 8.86E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_020342 SLC39A10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6714748 1.98E-05 NBL-GWAS version 2 dbGaP|2895
NM_020342 SLC39A10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4505549 4.83E-06 NBL-GWAS version 2 dbGaP|2895
NM_020344 SLC24A2 19187332 http://www.ncbi.nlm.nih.gov/pubmed/19187332 Asthma rs16937883 7.00E-06 Alpha-T-catenin (CTNNA3) gene was identified as a risk variant for toluene diisocyanate-induced asthma by genome-wide association analysis. NHGRI|-1
NM_020346 SLC17A6 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2593693 3.40E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_020347 LZTFL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs12639224 7.43E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020350 AGTRAP 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs4846033 4.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_020351 COL8A1 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs13095226 3.00E-06 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_020351 COL8A1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs2670321 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_020351 COL8A1 20686651 http://www.ncbi.nlm.nih.gov/pubmed/20686651 Cornea rs13070584 2.00E-06 Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases. NHGRI|-1
NM_020354 ENTPD7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11813439 3.15E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_020360 PLSCR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4613118 8.86E-05 NBL-GWAS version 2 dbGaP|2895
NM_020371 AVEN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs525243 6.15E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_020373 ANO2 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs12579350 4.00E-09 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_020374 C12orf4 20558539 http://www.ncbi.nlm.nih.gov/pubmed/20558539 Phosphorus rs2970818 4.00E-09 Common genetic variants associate with serum phosphorus concentration. NHGRI|-1
NM_020375 C12orf5 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs10849033 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_020387 RAB25 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs34372695 4.00E-12 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_020389 TRPC7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2673926 8.27E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_020389 TRPC7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2673925 7.34E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_020389 TRPC7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2673913 8.51E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_020395 INTS12 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs11727189 5.00E-17 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_020397 CAMK1D 20862305 http://www.ncbi.nlm.nih.gov/pubmed/20862305 "Diabetes Mellitus, Type 2" rs10906115 1.00E-08 Identification of new genetic risk variants for type 2 diabetes. NHGRI|-1
NM_020397 CAMK1D 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs12779790 1.00E-10 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_020397 CAMK1D 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11257695 1.67E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_020397 CAMK1D 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11257695 5.30E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_020403 PCDH9 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17081231 7.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_020403 PCDH9 17903300 http://www.ncbi.nlm.nih.gov/pubmed/17903300 Body Mass Index rs1333026 8.00E-06 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. NHGRI|-1
NM_020403 PCDH9 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs1585440 9.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_020429 SMURF1 20228798 http://www.ncbi.nlm.nih.gov/pubmed/20228798 "Colitis, Ulcerative" rs7809799 9.00E-11 Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). NHGRI|-1
NM_020431 TMEM63C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17750404 6.40E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_020433 JPH2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6073330 3.85E-05 NBL-GWAS version 2 dbGaP|2895
NM_020440 PTGFRN 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs2806864 6.00E-07 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264303 7.62E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264302 7.39E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264301 7.62E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1264298 7.62E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9262288 6.65E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs111872682 6.72E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs75893422 8.03E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113373192 6.65E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2517467 2.25E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2517467 8.78E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2074506 5.71E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs753725 2.01E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs753725 1.05E-05 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2532938 7.71E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020442 VARS2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs4678 4.59E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2532934 2.37E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2532934 8.78E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020442 VARS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2532929 1.51E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020443 NAV1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1854077 4.46E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020443 NAV1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs614452 1.02E-04 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020443 NAV1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs16865416 5.11E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020443 NAV1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs545372 8.92E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020443 NAV1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs625436 8.92E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020443 NAV1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs495198 2.19E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_020444 KIAA1191 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3749804 3.54E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_020444 KIAA1191 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11134974 4.26E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_020444 KIAA1191 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10063877 3.75E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_020445 ACTR3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs56216502 4.67E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_020453 ATP10D 19798445 http://www.ncbi.nlm.nih.gov/pubmed/19798445 Glucosylceramides rs10938494 8.00E-19 Genetic determinants of circulating sphingolipid concentrations in European populations. NHGRI|-1
NM_020455 GPR126 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs6570507 2.00E-07 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_020455 GPR126 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs6570507 4.00E-11 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_020455 GPR126 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs4896582 2.00E-18 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_020455 GPR126 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs3817928 1.00E-09 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_020455 GPR126 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs3748069 5.00E-14 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_020455 GPR126 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs9496398 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_020455 GPR126 21060863 http://www.ncbi.nlm.nih.gov/pubmed/21060863 Retinal Vein rs225717 1.00E-16 "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo." NHGRI|-1
NM_020458 TTC7A 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs17540621 2.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_020458 TTC7A 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs10194115 5.00E-07 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_020463 SMEK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Blood Pressure rs10496050 1.28E-05 Genomewide association analysis of systolic blood pressure (SBP) in a birth cohort from a founder population dbGaP|2903
NM_020464 NHSL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17067596 1.44E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_020464 NHSL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4895529 9.24E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_020469 ABO 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs8176746 4.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs8176732 1.67E-07 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2073824 1.26E-06 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs8176720 7.24E-07 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs8176717 1.11E-07 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs8176714 1.42E-07 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs512770 9.37E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs641943 1.06E-07 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs514708 1.06E-07 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs549446 2.96E-07 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs624601 1.08E-07 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs574347 1.25E-07 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs688976 1.36E-06 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs687621 7.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2073828 4.07E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2073828 5.64E-07 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs8176694 7.42E-07 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs657152 2.00E-30 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs657152 4.53E-18 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs657152 2.06E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_020469 ABO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs657152 5.59E-07 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_020469 ABO 20529992 http://www.ncbi.nlm.nih.gov/pubmed/20529992 Phytosterols rs657152 9.00E-13 Genetic regulation of serum phytosterol levels and risk of coronary artery disease. NHGRI|-1
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs8176682 1.06E-04 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 21239051 http://www.ncbi.nlm.nih.gov/pubmed/21239051 Cardiovascular Diseases rs514659 8.00E-09 Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. NHGRI|-1
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs644234 2.78E-18 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs500498 3.38E-08 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs505922 1.93E-19 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs505922 2.48E-06 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_020469 ABO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs505922 3.77E-08 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_020469 ABO 19648918 http://www.ncbi.nlm.nih.gov/pubmed/19648918 Pancreatic Neoplasms rs505922 5.00E-08 Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer. NHGRI|-1
NM_020469 ABO 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Tumor Necrosis Factor-alpha rs505922 7.00E-40 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_020469 ABO 19278955 http://www.ncbi.nlm.nih.gov/pubmed/19278955 Venous Thromboembolism rs505922 4.00E-15 Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach. NHGRI|-1
NM_020469 ABO 21533024 http://www.ncbi.nlm.nih.gov/pubmed/21533024 Intercellular Adhesion Molecule-1 rs507666 3.00E-91 "Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci." NHGRI|-1
NM_020469 ABO 18604267 http://www.ncbi.nlm.nih.gov/pubmed/18604267 Intercellular Adhesion Molecule-1 rs507666 5.00E-29 "Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women." NHGRI|-1
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs630014 9.65E-13 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs630014 4.28E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_020469 ABO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs630014 4.70E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs568203 3.40E-07 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 20147318 http://www.ncbi.nlm.nih.gov/pubmed/20147318 E-Selectin rs651007 2.00E-82 "Genetic variants in ABO blood group region, plasma soluble E-selectin levels and risk of type 2 diabetes." NHGRI|-1
NM_020469 ABO 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs579459 4.00E-14 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs579459 1.33E-29 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs579459 1.00E-29 Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectin. NHGRI|-1
NM_020469 ABO 20167578 http://www.ncbi.nlm.nih.gov/pubmed/20167578 P-Selectin rs579459 2.00E-41 Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. NHGRI|-1
NM_020469 ABO 20167578 http://www.ncbi.nlm.nih.gov/pubmed/20167578 Depression rs649129 1.00E-15 Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. NHGRI|-1
NM_020469 ABO 20066004 http://www.ncbi.nlm.nih.gov/pubmed/20066004 Angiotensin-Converting Enzyme Inhibitors rs495828 3.00E-08 A genome-wide association study identifies new loci for ACE activity: potential implications for response to ACE inhibitor. NHGRI|-1
NM_020469 ABO 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Count rs495828 3.00E-12 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_020469 ABO 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Count rs495828 4.00E-59 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_020469 ABO 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs495828 1.00E-11 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs495828 2.45E-26 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Hematocrit rs495828 6.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs500428 9.54E-08 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs558240 1.46E-09 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020469 ABO 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs7469576 1.05E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_020469 ABO 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11244053 7.53E-08 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020475 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs6474359 1.00E-08 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_020475 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs4737009 6.00E-12 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_020475 ANK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4466386 6.52E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_020476 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs6474359 1.00E-08 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_020476 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs4737009 6.00E-12 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_020476 ANK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4466386 6.52E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_020477 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs6474359 1.00E-08 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_020477 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs4737009 6.00E-12 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_020477 ANK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4466386 6.52E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_020478 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs6474359 1.00E-08 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_020478 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs4737009 6.00E-12 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_020478 ANK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4466386 6.52E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_020480 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs6474359 1.00E-08 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_020480 ANK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs4737009 6.00E-12 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_020480 ANK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4466386 6.52E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_020528 PCBP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2839020 6.58E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_020528 PCBP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9976523 7.46E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_020528 PCBP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs9980967 2.07E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_020528 PCBP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11701130 2.79E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_020528 PCBP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4819143 7.47E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_020536 CSRP2BP 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs17725255 2.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_020546 ADCY2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10512928 7.32E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_020546 ADCY2 18821564 http://www.ncbi.nlm.nih.gov/pubmed/18821564 Attention Deficit Disorder with Hyperactivity rs11134178 3.00E-06 Genome-wide association study of response to methylphenidate in 187 children with attention-deficit/hyperactivity disorder. NHGRI|-1
NM_020546 ADCY2 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs7729273 1.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_020546 ADCY2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6891243 2.10E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_020630 RET 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs2742234 4.00E-18 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_020630 RET 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs2142991 3.00E-07 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_020630 RET 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11239809 9.49E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_020630 RET 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2256432 8.11E-06 NBL-GWAS version 2 dbGaP|2895
NM_020632 ATP6V0A4 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs3800569 6.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_020632 ATP6V0A4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs366193 8.90E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_020647 JPH1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12679744 9.25E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_020648 TWSG1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1114591 3.23E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_020651 PELI1 21221998 http://www.ncbi.nlm.nih.gov/pubmed/21221998 Mucocutaneous Lymph Node Syndrome rs7604693 2.00E-06 A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease. NHGRI|-1
NM_020660 GJD2 20835239 http://www.ncbi.nlm.nih.gov/pubmed/20835239 Refractive Errors rs634990 2.00E-14 A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14. NHGRI|-1
NM_020673 RAB22A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs565990 1.50E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_020678 LRTM1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs358806 3.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_020682 AS3MT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11191425 3.96E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_020683 ADORA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10857899 3.06E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_020683 ADORA3 20548944 http://www.ncbi.nlm.nih.gov/pubmed/20548944 Bone Density rs494453 4.00E-08 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. NHGRI|-1
NM_020689 SLC24A3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs16980240 6.56E-07 NBL-GWAS version 1 dbGaP|2845
NM_020689 SLC24A3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1012646 7.47E-07 NBL-GWAS version 1 dbGaP|2845
NM_020689 SLC24A3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs3790171 3.64E-08 NBL-GWAS version 1 dbGaP|2845
NM_020689 SLC24A3 20031604 http://www.ncbi.nlm.nih.gov/pubmed/20031604 Matrix Metalloproteinases rs3790268 3.00E-07 Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels. NHGRI|-1
NM_020689 SLC24A3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs7272481 4.99E-08 NBL-GWAS version 1 dbGaP|2845
NM_020692 GALNTL1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 2.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_020692 GALNTL1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_020693 DSCAML1 19074352 http://www.ncbi.nlm.nih.gov/pubmed/19074352 Triglycerides rs10892151 3.00E-29 A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. NHGRI|-1
NM_020699 GATAD2B 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs4434872 8.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_020700 PPM1H 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs7302017 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_020716 GRAMD1B 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs735665 4.00E-12 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NM_020716 GRAMD1B 20639881 http://www.ncbi.nlm.nih.gov/pubmed/20639881 "Lymphoma, Follicular" rs735665 4.00E-09 Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. NHGRI|-1
NM_020716 GRAMD1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11219172 5.56E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_020716 GRAMD1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4936819 1.24E-06 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_020718 USP31 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs8049603 1.00E-06 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_020724 RNF150 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1550057 4.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_020731 AHRR 21602797 http://www.ncbi.nlm.nih.gov/pubmed/21602797 Cystic Fibrosis rs12188164 4.00E-06 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. NHGRI|-1
NM_020732 ARID1B 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs9478751 3.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_020732 ARID1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6917698 2.61E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_020732 ARID1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs288944 3.28E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_020732 ARID1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs288945 5.18E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_020732 ARID1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2817460 1.40E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_020732 ARID1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1246182 1.54E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_020737 LRFN2 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs10484761 7.00E-12 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_020738 KIDINS220 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs7587928 2.00E-07 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_020742 NLGN4X 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Fibrinogen rs7885458 3.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_020742 NLGN4X 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs5916687 3.00E-06 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_020744 MTA3 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs930421 6.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_020744 MTA3 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs6719977 2.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_020746 MAVS 20159242 http://www.ncbi.nlm.nih.gov/pubmed/20159242 Asthma rs4815617 8.00E-06 Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. NHGRI|-1
NM_020746 MAVS 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs4815617 8.00E-08 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_020747 ZNF608 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs11241713 3.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_020747 ZNF608 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2250107 3.01E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_020747 ZNF608 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1494672 2.82E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_020747 ZNF608 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1494673 1.76E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_020747 ZNF608 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1494671 4.84E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_020751 COG6 18369459 http://www.ncbi.nlm.nih.gov/pubmed/18369459 Psoriasis rs7993214 2.00E-06 A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. NHGRI|-1
NM_020751 COG6 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs9548988 3.00E-07 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_020751 COG6 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Alanine Transaminase rs10492681 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_020751 COG6 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs941823 4.00E-12 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_020751 COG6 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs2755237 1.00E-08 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_020751 COG6 20485516 http://www.ncbi.nlm.nih.gov/pubmed/20485516 Cornea rs2721051 5.00E-10 Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. NHGRI|-1
NM_020752 GPR158 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10508687 8.45E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_020754 ARHGAP31 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs11712165 8.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_020759 STARD9 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Thyroxine rs16957063 5.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_020760 HECW2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs13001220 2.99E-05 NBL-GWAS version 2 dbGaP|2895
NM_020760 HECW2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4850679 5.83E-05 NBL-GWAS version 2 dbGaP|2895
NM_020764 CASKIN1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs26868 9.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_020766 PCDH19 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs5921594 3.79E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4336470 7.91E-05 NBL-GWAS version 2 dbGaP|2895
NM_020771 HACE1 17903292 http://www.ncbi.nlm.nih.gov/pubmed/17903292 Thyrotropin rs9322817 7.00E-06 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_020771 HACE1 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7759938 5.00E-60 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_020771 HACE1 19448620 http://www.ncbi.nlm.nih.gov/pubmed/19448620 Menarche rs7759938 7.00E-09 Meta-analysis of genome-wide association data identifies two loci influencing age at menarche. NHGRI|-1
NM_020771 HACE1 19448622 http://www.ncbi.nlm.nih.gov/pubmed/19448622 Menarche rs314280 2.00E-14 Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche. NHGRI|-1
NM_020771 HACE1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs9377619 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs9377619 1.44E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs270666 6.19E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1341118 1.12E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs9391181 1.19E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs169282 7.76E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs447871 1.90E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs404900 2.77E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6571178 9.84E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs814372 1.37E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs549374 2.00E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7764670 2.19E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs9391184 2.39E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10499040 2.04E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs271878 2.75E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs271876 1.47E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020771 HACE1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4946463 7.31E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_020777 SORCS2 21216879 http://www.ncbi.nlm.nih.gov/pubmed/21216879 Insulin-Like Growth Factor Binding Protein 4 rs4234798 5.00E-10 A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. NHGRI|-1
NM_020777 SORCS2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs886374 2.38E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_020782 KLHDC5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7137085 3.38E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_020783 SYT4 21042317 http://www.ncbi.nlm.nih.gov/pubmed/21042317 "Depressive Disorder, Major" rs12457996 6.00E-06 "Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned." NHGRI|-1
NM_020783 SYT4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs610325 9.54E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_020783 SYT4 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs17664267 7.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_020785 CC2D2A 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1861050 8.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_020791 TAOK1 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs2138852 1.00E-22 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_020791 TAOK1 19110211 http://www.ncbi.nlm.nih.gov/pubmed/19110211 Platelet Count rs2138852 7.00E-28 A genome-wide association study identifies three loci associated with mean platelet volume. NHGRI|-1
NM_020794 LRRC7 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs4147141 6.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_020794 LRRC7 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs4147141 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_020794 LRRC7 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs4650135 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_020796 SEMA6A 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs7702057 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_020800 IFT80 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6441306 3.52E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020801 ARRDC3 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs933688 6.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_020801 ARRDC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6881283 5.58E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_020808 SIPA1L2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1547741 6.71E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_020808 SIPA1L2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4308924 7.97E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_020808 SIPA1L2 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, LDL" rs10746514 1.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_020808 SIPA1L2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs16856874 6.63E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_020808 SIPA1L2 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs669408 1.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_020812 DOCK6 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs4804155 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_020820 PREX1 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs6063312 2.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_020820 PREX1 21441931 http://www.ncbi.nlm.nih.gov/pubmed/21441931 Nephrotic Syndrome rs11086243 3.00E-06 Common variation in GPC5 is associated with acquired nephrotic syndrome. NHGRI|-1
NM_020821 VPS13C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4143844 4.93E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020821 VPS13C 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs17271305 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_020821 VPS13C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs3934516 5.53E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_020829 KIAA1432 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7026868 6.90E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_020829 KIAA1432 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs4740820 6.41E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020831 MKL1 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Body Height rs5757949 4.00E-06 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_020836 BEGAIN 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs6575793 1.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_020844 C8orf79 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Survival rs4831837 5.00E-07 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_020845 PITPNM2 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs1727307 3.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_020848 KIAA1462 21088011 http://www.ncbi.nlm.nih.gov/pubmed/21088011 Coronary Artery Disease rs3739998 1.00E-11 Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23. NHGRI|-1
NM_020848 KIAA1462 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs2505083 4.00E-08 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_020848 KIAA1462 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs2986971 3.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_020856 TSHZ3 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs1078373 6.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_020856 TSHZ3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2867743 1.84E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_020858 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs12594515 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_020858 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs12594515 7.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_020858 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4603502 3.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_020858 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1865648 1.57E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_020858 SEMA6D 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11857760 6.14E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_020859 SHROOM3 20383145 http://www.ncbi.nlm.nih.gov/pubmed/20383145 Kidney Diseases rs9992101 6.00E-09 Genetic loci influencing kidney function and chronic kidney disease. NHGRI|-1
NM_020859 SHROOM3 19430482 http://www.ncbi.nlm.nih.gov/pubmed/19430482 Creatinine rs17319721 1.00E-12 Multiple loci associated with indices of renal function and chronic kidney disease. NHGRI|-1
NM_020859 SHROOM3 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs17319721 1.00E-19 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_020859 SHROOM3 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs13146355 6.00E-13 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_020859 SHROOM3 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs13106227 4.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_020859 SHROOM3 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs1986734 1.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_020859 SHROOM3 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs344135 4.18E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_020859 SHROOM3 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs3733242 2.09E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_020860 STIM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12505133 3.78E-05 NBL-GWAS version 2 dbGaP|2895
NM_020860 STIM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs11727649 1.88E-05 NBL-GWAS version 2 dbGaP|2895
NM_020863 ZFAT 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1036819 1.00E-24 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_020863 ZFAT 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs12680655 2.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_020863 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1545240 1.52E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_020863 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs16905215 1.89E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_020863 ZFAT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs9785140 1.26E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_020864 KIAA1486 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7578326 5.00E-20 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_020864 KIAA1486 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs2943634 2.00E-07 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_020864 KIAA1486 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs2943641 9.00E-12 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_020864 KIAA1486 21706003 http://www.ncbi.nlm.nih.gov/pubmed/21706003 Adiposity rs2943650 4.00E-11 Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile. NHGRI|-1
NM_020864 KIAA1486 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs964818 4.37E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_020864 KIAA1486 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4510219 4.86E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_020864 KIAA1486 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3914465 1.85E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_020864 KIAA1486 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs13032261 4.49E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_020864 KIAA1486 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4129068 2.87E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_020864 KIAA1486 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4129068 5.82E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_020864 KIAA1486 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs11903929 4.37E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_020864 KIAA1486 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs1517484 5.00E-07 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_020866 KLHL1 17903298 http://www.ncbi.nlm.nih.gov/pubmed/17903298 Insulin Resistance rs2066219 9.00E-06 Genome-wide association with diabetes-related traits in the Framingham Heart Study. NHGRI|-1
NM_020866 KLHL1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs17605645 9.21E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_020868 DPP10 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4624391 9.77E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_020868 DPP10 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4277531 9.40E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_020873 LRRN1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4055307 1.85E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_020873 LRRN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9829721 6.83E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_020873 LRRN1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs1601875 7.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_020877 DNAH2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs16956936 5.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_020894 KIAA1530 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs13118159 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_020896 OSBPL5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4758533 4.82E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_020898 CALCOCO1 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs941184 3.00E-07 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_020898 CALCOCO1 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs7969151 2.00E-06 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_020898 CALCOCO1 20460270 http://www.ncbi.nlm.nih.gov/pubmed/20460270 Biliary Atresia rs2120991 9.00E-06 Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. NHGRI|-1
NM_020901 PHRF1 18204446 http://www.ncbi.nlm.nih.gov/pubmed/18204446 "Lupus Erythematosus, Systemic" rs4963128 3.00E-10 "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci." NHGRI|-1
NM_020901 PHRF1 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs4963128 4.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_020905 RDH14 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2345089 5.11E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_020905 RDH14 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs16984239 2.00E-06 Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_020905 RDH14 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs16984239 6.04E-06 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_020905 RDH14 18084291 http://www.ncbi.nlm.nih.gov/pubmed/18084291 Amyotrophic Lateral Sclerosis rs7580332 9.00E-06 Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis. NHGRI|-1
NM_020908 TLE3 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs6494849 7.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_020910 KIAA1549 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12670097 2.85E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_020910 KIAA1549 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12670097 9.68E-06 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_020911 PLXNA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3734991 1.62E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_020911 PLXNA4 17903300 http://www.ncbi.nlm.nih.gov/pubmed/17903300 Body Mass Index rs1106683 1.00E-07 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. NHGRI|-1
NM_020911 PLXNA4 17903300 http://www.ncbi.nlm.nih.gov/pubmed/17903300 Body Mass Index rs1106684 2.00E-06 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. NHGRI|-1
NM_020914 RNF213 21048783 http://www.ncbi.nlm.nih.gov/pubmed/21048783 Moyamoya Disease rs6565681 2.00E-08 A genome-wide association study identifies RNF213 as the first Moyamoya disease gene. NHGRI|-1
NM_020918 GPAM 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3107346 4.85E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_020918 GPAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6585111 3.85E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_020927 VAT1L 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs435746 3.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_020927 VAT1L 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11647294 5.34E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_020927 VAT1L 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs16946737 5.34E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_020929 LRRC4C 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs4611189 6.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_020929 LRRC4C 20548944 http://www.ncbi.nlm.nih.gov/pubmed/20548944 Osteoporosis rs12808199 9.00E-07 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. NHGRI|-1
NM_020929 LRRC4C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs6485172 1.39E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_020929 LRRC4C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10837325 1.73E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_020943 CWC22 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs1072038 3.86E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_020943 CWC22 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs16867321 2.00E-06 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_020943 CWC22 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs918959 2.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_020945 WDFY4 19165918 http://www.ncbi.nlm.nih.gov/pubmed/19165918 "Lupus Erythematosus, Systemic" rs11101442 3.00E-06 Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. NHGRI|-1
NM_020945 WDFY4 20169177 http://www.ncbi.nlm.nih.gov/pubmed/20169177 "Lupus Erythematosus, Systemic" rs7097397 8.00E-12 Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus. NHGRI|-1
NM_020945 WDFY4 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 "Aorta, Abdominal" rs3849150 2.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_020945 WDFY4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3849150 2.73E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_020945 WDFY4 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs1913517 7.00E-12 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_020946 DENND1A 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Personality rs7852296 9.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_020946 DENND1A 21151128 http://www.ncbi.nlm.nih.gov/pubmed/21151128 Polycystic Ovary Syndrome rs10818854 9.00E-18 "Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3." NHGRI|-1
NM_020946 DENND1A 21151128 http://www.ncbi.nlm.nih.gov/pubmed/21151128 Polycystic Ovary Syndrome rs2479106 8.00E-19 "Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3." NHGRI|-1
NM_020947 KIAA1609 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs371915 2.00E-08 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_020949 SLC7A14 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs6444931 6.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_020949 SLC7A14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6444931 1.96E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_020952 TRPM3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4745062 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_020952 TRPM3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12350232 8.34E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_020954 RNF213 21048783 http://www.ncbi.nlm.nih.gov/pubmed/21048783 Moyamoya Disease rs6565681 2.00E-08 A genome-wide association study identifies RNF213 as the first Moyamoya disease gene. NHGRI|-1
NM_020975 RET 19196962 http://www.ncbi.nlm.nih.gov/pubmed/19196962 Hirschsprung Disease rs2742234 4.00E-18 Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. NHGRI|-1
NM_020975 RET 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs2142991 3.00E-07 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_020975 RET 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11239809 9.49E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_020975 RET 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2256432 8.11E-06 NBL-GWAS version 2 dbGaP|2895
NM_020977 ANK2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4834308 6.98E-06 NBL-GWAS version 1 dbGaP|2845
NM_020987 ANK3 20185149 http://www.ncbi.nlm.nih.gov/pubmed/20185149 Schizophrenia rs10761482 8.00E-06 Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. NHGRI|-1
NM_020987 ANK3 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs10994336 9.00E-09 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_020987 ANK3 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs10994338 5.00E-07 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_020989 CRYGC 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2242073 8.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_020998 MST1 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs3197999 1.00E-16 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_020998 MST1 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs3197999 4.00E-09 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_020998 MST1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs3197999 1.00E-12 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_020998 MST1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs3197999 6.00E-17 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_021005 NR2F2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs2567426 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_021005 NR2F2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Hypertension rs2398162 6.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_021007 SCN2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2116658 1.48E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_021007 SCN2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs13025009 2.16E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_021007 SCN2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs764660 7.83E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_021018 HIST1H3E 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs10946808 4.00E-17 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_021018 HIST1H3E 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs10946808 6.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_021018 HIST1H3E 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs10946808 6.00E-12 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_021021 SNTB1 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs11989782 7.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_021023 CFHR3 20694013 http://www.ncbi.nlm.nih.gov/pubmed/20694013 Meningococcal Infections rs426736 5.00E-13 Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease. NHGRI|-1
NM_021026 RFPL1 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Carotid Artery Diseases rs13053817 2.00E-06 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_021027 UGT1A9 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs2602381 4.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_021027 UGT1A9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1604144 4.75E-05 NBL-GWAS version 2 dbGaP|2895
NM_021027 UGT1A9 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs887829 1.00E-69 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_021027 UGT1A9 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs6742078 5E-324 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_021027 UGT1A9 21646302 http://www.ncbi.nlm.nih.gov/pubmed/21646302 Bilirubin rs4148325 5.00E-62 Mayo genome consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. NHGRI|-1
NM_021032 FGF12 21139019 http://www.ncbi.nlm.nih.gov/pubmed/21139019 Carcinoid Tumor rs975121 7.00E-06 A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum. NHGRI|-1
NM_021032 FGF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs9859577 9.87E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_021032 FGF12 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Phosphatidylcholines rs4453795 4.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_021032 FGF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2886785 9.60E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_021032 FGF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9873551 5.37E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_021032 FGF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6444558 1.54E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_021032 FGF12 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7635839 3.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_021058 HIST1H2BJ 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs13194491 1.00E-08 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_021064 HIST1H2AH 19571811 http://www.ncbi.nlm.nih.gov/pubmed/19571811 Schizophrenia rs13194053 1.00E-08 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. NHGRI|-1
NM_021064 HIST1H2AH 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs13194053 1.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_021072 HCN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs4866929 7.17E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_021072 HCN1 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs981782 9.00E-06 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_021072 HCN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6874279 5.08E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_021072 HCN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs559096 9.08E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_021072 HCN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1674512 9.15E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_021072 HCN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4865676 9.06E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_021072 HCN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10064702 9.15E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_021072 HCN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7710841 9.06E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_021072 HCN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10042504 9.15E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_021072 HCN1 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs7716600 7.00E-07 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_021072 HCN1 20686651 http://www.ncbi.nlm.nih.gov/pubmed/20686651 Cornea rs10941694 9.00E-06 Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases. NHGRI|-1
NM_021076 NEFH 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Carotid Artery Diseases rs13053817 2.00E-06 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_021080 DAB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11206955 2.19E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_021080 DAB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11810899 2.01E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_021080 DAB1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs10159302 9.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_021090 MTMR3 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs36600 6.00E-13 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_021094 SLCO1A2 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs11568563 7.00E-08 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_021097 SLC8A1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs977867 4.31E-06 NBL-GWAS version 1 dbGaP|2845
NM_021097 SLC8A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7569590 3.30E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_021097 SLC8A1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs719593 5.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_021101 CLDN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs16865151 1.71E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_021101 CLDN1 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs16865258 2.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_021109 TMSB4X 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs5979785 6.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_021115 SEZ6L 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Coronary Disease rs688034 4.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_021115 SEZ6L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs667577 8.58E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_021115 SEZ6L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2049988 1.28E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_021117 CRY2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs11605924 1.00E-14 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_021127 PMAIP1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs11665646 2.20E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_021127 PMAIP1 21106707 http://www.ncbi.nlm.nih.gov/pubmed/21106707 Bleomycin rs8093763 3.00E-08 A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity. NHGRI|-1
NM_021136 RTN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17804446 1.83E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_021136 RTN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11158264 2.54E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_021145 DMTF1 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs11773103 1.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_021149 COTL1 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs371915 2.00E-08 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_021150 GRIP1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs1082714 5.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_021158 TRIB3 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs6051520 2.00E-07 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_021159 RAP1GDS1 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Triglycerides rs10516430 6.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_021160 BAT5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2295663 8.40E-24 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_021161 KCNK10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12434331 6.34E-05 NBL-GWAS version 2 dbGaP|2895
NM_021161 KCNK10 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs17124581 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_021165 FAM5B 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs633715 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_021165 FAM5B 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs543874 4.00E-23 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_021168 RAB40C 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs763014 5.00E-06 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_021176 G6PC2 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs1402837 5.00E-10 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_021176 G6PC2 19060907 http://www.ncbi.nlm.nih.gov/pubmed/19060907 Blood Glucose rs560887 1.00E-57 Variants in MTNR1B influence fasting glucose levels. NHGRI|-1
NM_021176 G6PC2 18451265 http://www.ncbi.nlm.nih.gov/pubmed/18451265 Blood Glucose rs560887 4.00E-23 A polymorphism within the G6PC2 gene is associated with fasting plasma glucose levels. NHGRI|-1
NM_021176 G6PC2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs560887 9.00E-218 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_021176 G6PC2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs560887 2.00E-66 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_021176 G6PC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs560887 5.69E-10 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_021176 G6PC2 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Glucose rs560887 6.00E-10 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_021176 G6PC2 18521185 http://www.ncbi.nlm.nih.gov/pubmed/18521185 Blood Glucose rs563694 4.00E-07 Variations in the G6PC2/ABCB11 genomic region are associated with fasting glucose levels. NHGRI|-1
NM_021176 G6PC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Glucose rs563694 1.17E-07 Genomewide association analysis of glucose (GLU) in a birth cohort from a founder population dbGaP|2899
NM_021180 GRHL3 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs4649203 7.00E-08 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_021182 HMHB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11167821 7.98E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_021182 HMHB1 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs17100498 5.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_021184 C6orf47 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3130617 6.29E-135 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_021186 ZP4 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs2499604 2.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_021189 CADM3 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Chemokine CCL2 rs1474747 3.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_021190 PTBP2 19571811 http://www.ncbi.nlm.nih.gov/pubmed/19571811 Schizophrenia rs7544736 6.00E-07 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. NHGRI|-1
NM_021199 SQRDL 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs12594515 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_021199 SQRDL 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs12594515 7.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_021199 SQRDL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4603502 3.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_021199 SQRDL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1865648 1.57E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_021199 SQRDL 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11857760 6.14E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_021200 PLEKHB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs593927 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_021203 SRPRB 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs1534166 2.00E-17 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_021203 SRPRB 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1830084 1.00E-09 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_021205 RHOU 20844546 http://www.ncbi.nlm.nih.gov/pubmed/20844546 Endometriosis rs801112 5.00E-06 Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population. NHGRI|-1
NM_021205 RHOU 18849993 http://www.ncbi.nlm.nih.gov/pubmed/18849993 "Carcinoma, Basal Cell" rs801114 6.00E-12 Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits. NHGRI|-1
NM_021205 RHOU 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs603404 7.84E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_021205 RHOU 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs603404 9.02E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_021205 RHOU 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10916407 9.09E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_021213 PCTP 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs1431318 9.00E-07 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_021213 PCTP 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs8065311 2.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_021214 FAM108C1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12593088 7.11E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_021215 RPRD1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6022716 7.11E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_021215 RPRD1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6023059 6.26E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_021219 JAM2 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs17001239 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_021224 ZNF462 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs4743034 2.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_021224 ZNF462 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Alanine Transaminase rs4742971 8.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_021224 ZNF462 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10816353 3.44E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_021224 ZNF462 19448621 http://www.ncbi.nlm.nih.gov/pubmed/19448621 Menarche rs7861820 3.00E-09 Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. NHGRI|-1
NM_021224 ZNF462 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs2090409 2.00E-33 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_021224 ZNF462 19448620 http://www.ncbi.nlm.nih.gov/pubmed/19448620 Menarche rs2090409 2.00E-09 Meta-analysis of genome-wide association data identifies two loci influencing age at menarche. NHGRI|-1
NM_021224 ZNF462 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10759199 9.45E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_021226 ARHGAP22 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs4838605 2.00E-09 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_021226 ARHGAP22 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs10776612 2.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_021255 PELI2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1188157 1.23E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_021255 PELI2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs922656 6.05E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_021255 PELI2 21460395 http://www.ncbi.nlm.nih.gov/pubmed/21460395 Telomere length rs398652 2.00E-06 A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer. NHGRI|-1
NM_021574 BCR 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs5751614 6.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_021599 ADAMTS2 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs10039254 8.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_021614 KCNN2 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs17135859 8.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_021614 KCNN2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs4621553 4.00E-08 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_021620 PRDM13 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs4840086 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_021620 PRDM13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4431442 5.59E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751890 1.61E-15 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751890 2.15E-16 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_021622 PLEKHA1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs6585827 2.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6585827 1.12E-21 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6585827 1.42E-23 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2280141 1.06E-21 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2280141 1.37E-23 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2292627 2.68E-17 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2292627 4.68E-18 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1882907 4.02E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1882907 6.27E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7091160 1.81E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6585818 1.92E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11598094 2.21E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11598094 5.64E-07 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7080960 4.24E-11 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7080960 5.76E-12 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11200583 5.76E-16 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11200583 8.67E-16 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751889 1.73E-14 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_021622 PLEKHA1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751889 2.26E-15 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_021642 FCGR2A 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 "Colitis, Ulcerative" rs1801274 2.00E-12 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_021642 FCGR2A 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs1801274 2.00E-20 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_021642 FCGR2A 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs10800309 3.00E-09 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_021643 TRIB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs17551939 8.49E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_021643 TRIB2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs10929808 4.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_021643 TRIB2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs1534422 2.00E-06 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_021647 MFAP3L 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4692758 9.61E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_021727 FADS3 19798445 http://www.ncbi.nlm.nih.gov/pubmed/19798445 Sphingomyelins rs1000778 7.00E-13 Genetic determinants of circulating sphingolipid concentrations in European populations. NHGRI|-1
NM_021734 SLC25A19 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs9892996 2.23E-07 NBL-GWAS version 1 dbGaP|2845
NM_021735 CLCN6 21273288 http://www.ncbi.nlm.nih.gov/pubmed/21273288 "Natriuretic Peptide, Brain" rs1023252 4.00E-16 Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. NHGRI|-1
NM_021736 CLCN6 21273288 http://www.ncbi.nlm.nih.gov/pubmed/21273288 "Natriuretic Peptide, Brain" rs1023252 4.00E-16 Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. NHGRI|-1
NM_021737 CLCN6 21273288 http://www.ncbi.nlm.nih.gov/pubmed/21273288 "Natriuretic Peptide, Brain" rs1023252 4.00E-16 Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. NHGRI|-1
NM_021738 SVIL 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1927457 8.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_021777 ADAM28 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs10109414 1.00E-08 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_021783 EDA2R 18849991 http://www.ncbi.nlm.nih.gov/pubmed/18849991 Alopecia rs6625163 5.00E-11 Male-pattern baldness susceptibility locus at 20p11. NHGRI|-1
NM_021797 CHIA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17654531 1.16E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_021798 IL21R 19874204 http://www.ncbi.nlm.nih.gov/pubmed/19874204 Bone Density rs8057551 2.00E-06 IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study. NHGRI|-1
NM_021803 IL21 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs6852535 1.00E-07 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_021803 IL21 17558408 http://www.ncbi.nlm.nih.gov/pubmed/17558408 Celiac Disease rs6822844 1.00E-14 A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21. NHGRI|-1
NM_021803 IL21 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs6822844 3.00E-13 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_021803 IL21 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs7682241 4.00E-08 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_021807 EXOC4 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs10488172 8.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_021813 BACH2 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs10806425 4.00E-10 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_021813 BACH2 18840781 http://www.ncbi.nlm.nih.gov/pubmed/18840781 "Diabetes Mellitus, Type 1" rs3757247 1.00E-06 Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes. NHGRI|-1
NM_021813 BACH2 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs11755527 5.00E-12 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_021813 BACH2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs11755527 5.00E-08 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_021813 BACH2 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs1847472 5.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_021813 BACH2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1145724 4.14E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_021813 BACH2 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs806276 3.00E-07 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_021814 ELOVL5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2281274 3.14E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_021814 ELOVL5 20363506 http://www.ncbi.nlm.nih.gov/pubmed/20363506 Cardiovascular Diseases rs735860 4.00E-06 Genome-wide association study of normal tension glaucoma: common variants in SRBD1 and ELOVL5 contribute to disease susceptibility. NHGRI|-1
NM_021823 PPCDC 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs12148488 6.00E-07 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_021870 FGG 18823527 http://www.ncbi.nlm.nih.gov/pubmed/18823527 Alzheimer Disease rs727153 3.00E-06 A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. NHGRI|-1
NM_021870 FGG 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs13109457 3.00E-18 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_021871 FGA 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs13109457 3.00E-18 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_021872 CDC25B 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Bipolar Disorder rs3761218 7.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_021873 CDC25B 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Bipolar Disorder rs3761218 7.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_021907 DTNB 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11684202 6.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_021912 GABRB3 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs8043440 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_021912 GABRB3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs3212335 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_021923 FGFRL1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6839931 2.09E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_021923 FGFRL1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7669622 4.53E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_021923 FGFRL1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6827357 5.15E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_021925 C2orf43 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs13385191 8.00E-08 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_021925 C2orf43 21059979 http://www.ncbi.nlm.nih.gov/pubmed/21059979 "Cholesterol, LDL" rs4971516 2.00E-52 Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish. NHGRI|-1
NM_021925 C2orf43 21059979 http://www.ncbi.nlm.nih.gov/pubmed/21059979 Cholesterol rs4971516 2.00E-40 Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish. NHGRI|-1
NM_021925 C2orf43 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7569328 1.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_021925 C2orf43 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs3923037 2.29E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_021925 C2orf43 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs3923037 2.34E-06 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_021925 C2orf43 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs11902417 4.00E-07 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_021925 C2orf43 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs6544366 2.00E-07 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_021925 C2orf43 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, HDL" rs6754295 4.00E-08 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_021925 C2orf43 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs6754295 3.78E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_021925 C2orf43 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs6754295 1.40E-08 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_021925 C2orf43 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Triglycerides rs6754295 3.00E-08 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_021925 C2orf43 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs6754295 9.47E-08 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_021925 C2orf43 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs7557067 9.00E-12 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_021937 EEFSEC 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs2687729 1.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_021937 EEFSEC 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs10934853 3.00E-10 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_021938 CELF5 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs11669592 4.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_021943 ZFAND3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6901928 9.73E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_021945 SLC22A23 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs4959235 2.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NM_021945 SLC22A23 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs17309827 7.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_021947 SRR 20174558 http://www.ncbi.nlm.nih.gov/pubmed/20174558 "Diabetes Mellitus, Type 2" rs391300 3.00E-09 A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. NHGRI|-1
NM_021948 BCAN 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs11360 3.57E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_021951 DMRT1 21551455 http://www.ncbi.nlm.nih.gov/pubmed/21551455 Germinoma rs7040024 1.00E-11 A second independent locus within DMRT1 is associated with testicular germ cell tumor susceptibility. NHGRI|-1
NM_021951 DMRT1 21551455 http://www.ncbi.nlm.nih.gov/pubmed/21551455 Germinoma rs755383 9.00E-10 A second independent locus within DMRT1 is associated with testicular germ cell tumor susceptibility. NHGRI|-1
NM_021951 DMRT1 20543847 http://www.ncbi.nlm.nih.gov/pubmed/20543847 Testicular Neoplasms rs755383 1.00E-23 "Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer." NHGRI|-1
NM_021956 GRIK2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1361168 7.90E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_021956 GRIK2 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Fibrinogen rs12207601 2.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_021956 GRIK2 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs4520040 3.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_021958 HLX 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs12733856 3.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_021958 HLX 20971583 http://www.ncbi.nlm.nih.gov/pubmed/20971583 Dupuytren Contracture rs12032381 6.00E-06 Genome-wide association scan of Dupuytren's disease. NHGRI|-1
NM_021958 HLX 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs12073837 2.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_021958 HLX 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs11118620 7.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_021959 PPP1R11 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs3807031 1.10E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_021966 TCL1A 21172079 http://www.ncbi.nlm.nih.gov/pubmed/21172079 Aromatase Inhibitors rs11849538 7.00E-07 Genome-wide case-control study of musculoskeletal adverse events and functional genomics in women receiving aromatase inhibitors: going beyond associations. NHGRI|-1
NM_021966 TCL1A 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs2369304 9.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_021966 TCL1A 20876420 http://www.ncbi.nlm.nih.gov/pubmed/20876420 Aromatase Inhibitors rs7158782 8.00E-07 Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors. NHGRI|-1
NM_021977 SLC22A3 21493818 http://www.ncbi.nlm.nih.gov/pubmed/21493818 Monocyte early outgrowth colony forming units rs402219 6.00E-07 Genetic and clinical correlates of early-outgrowth colony-forming units. NHGRI|-1
NM_021977 SLC22A3 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs9364554 6.00E-10 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_021977 SLC22A3 21242260 http://www.ncbi.nlm.nih.gov/pubmed/21242260 Colonic Neoplasms rs7758229 8.00E-09 Common variant in 6q26-q27 is associated with distal colon cancer in an Asian population. NHGRI|-1
NM_021977 SLC22A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs410569 2.45E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_021977 SLC22A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs446809 6.51E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_021977 SLC22A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs667538 3.09E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_021977 SLC22A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs415897 2.91E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_021977 SLC22A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs384156 9.10E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_021977 SLC22A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs316169 5.08E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_021977 SLC22A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs316170 2.21E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_021980 OPTN 20436471 http://www.ncbi.nlm.nih.gov/pubmed/20436471 Osteitis Deformans rs1561570 6.00E-13 "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone." NHGRI|-1
NM_021980 OPTN 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs1561570 4.00E-38 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_021980 OPTN 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs525455 7.00E-07 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_021982 SEC24A 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs246341 7.72E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_021996 GBGT1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs6597604 7.23E-06 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_021998 ZNF711 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2285602 2.37E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_021998 ZNF711 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2188734 4.65E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_022055 KCNK12 19890347 http://www.ncbi.nlm.nih.gov/pubmed/19890347 Vitiligo rs6544997 7.00E-06 "Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8." NHGRI|-1
NM_022062 PKNOX2 21703634 http://www.ncbi.nlm.nih.gov/pubmed/21703634 Alcoholism rs750338 1.00E-06 A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence. NHGRI|-1
NM_022062 PKNOX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs585977 6.15E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_022063 C10orf84 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11198446 7.49E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_022065 THADA 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs7590268 9.00E-08 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_022065 THADA 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs1465618 2.00E-08 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_022065 THADA 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs6732426 1.00E-07 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_022065 THADA 21151128 http://www.ncbi.nlm.nih.gov/pubmed/21151128 Polycystic Ovary Syndrome rs13429458 2.00E-23 "Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3." NHGRI|-1
NM_022065 THADA 21151128 http://www.ncbi.nlm.nih.gov/pubmed/21151128 Polycystic Ovary Syndrome rs12478601 3.00E-23 "Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3." NHGRI|-1
NM_022065 THADA 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7578597 1.00E-09 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_022065 THADA 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs10495903 2.00E-14 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_022068 FAM38B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1032061 1.55E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_022068 FAM38B 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2276371 8.84E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_022073 EGLN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1680730 1.71E-05 NBL-GWAS version 2 dbGaP|2895
NM_022075 LASS2 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs267734 1.00E-12 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_022088 ZFP64 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs6013382 5.00E-06 Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_022088 ZFP64 19478329 http://www.ncbi.nlm.nih.gov/pubmed/19478329 "Infertility, Male" rs6068020 5.00E-07 Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. NHGRI|-1
NM_022089 ATP13A2 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs3738814 2.00E-07 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_022093 TNN 21703634 http://www.ncbi.nlm.nih.gov/pubmed/21703634 Alcoholism rs6701037 2.00E-07 A meta-analysis of two genome-wide association studies identifies 3 new loci for alcohol dependence. NHGRI|-1
NM_022097 CHP2 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4968031 1.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_022104 PCIF1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs7679 4.00E-09 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_022104 PCIF1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs7679 7.00E-11 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_022107 GPSM3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs176095 2.18E-12 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_022107 GPSM3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs204991 1.05E-08 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_022107 GPSM3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs8192583 2.25E-20 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_022110 FKBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7383258 1.51E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_022110 FKBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9296009 1.19E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_022111 CLSPN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs577483 3.31E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_022111 CLSPN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs535638 3.92E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_022114 PRDM16 21666692 http://www.ncbi.nlm.nih.gov/pubmed/21666692 Migraine Disorders rs2651899 4.00E-09 Genome-wide association study reveals three susceptibility loci for common migraine in the general population. NHGRI|-1
NM_022114 PRDM16 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2651916 1.93E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_022114 PRDM16 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10737190 2.04E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_022114 PRDM16 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs6658356 2.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_022115 PRDM15 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs7279297 3.00E-06 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_022116 FIGNL1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs12718597 5.00E-13 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_022118 RBM26 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7988279 3.05E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_022123 NPAS3 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Mental Disorders rs4982029 4.00E-06 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_022123 NPAS3 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs8015959 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_022123 NPAS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs8014514 1.79E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_022123 NPAS3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17555909 6.53E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_022123 NPAS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17571355 2.92E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_022123 NPAS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs10142154 2.34E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_022127 SLC28A3 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, HDL" rs10123041 6.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_022129 PBLD 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1900004 2.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_022129 PBLD 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1900004 3.00E-35 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_022129 PBLD 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs3858145 2.00E-07 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_022129 PBLD 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Optic Disk rs3858145 3.00E-10 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_022129 PBLD 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Optic Disk rs12571093 2.00E-10 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_022131 CLSTN2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs6439924 2.89E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_022131 CLSTN2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs11708189 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_022136 SAMSN1 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs1006899 6.00E-06 New sequence variants associated with bone mineral density. NHGRI|-1
NM_022137 SMOC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs227446 9.90E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_022138 SMOC2 19890347 http://www.ncbi.nlm.nih.gov/pubmed/19890347 Vitiligo rs13208776 9.00E-08 "Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8." NHGRI|-1
NM_022138 SMOC2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7741751 2.25E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_022140 EPB41L4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10515444 4.80E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_022140 EPB41L4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3985058 4.80E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_022143 LRRC4 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4731416 6.23E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_022144 TNMD 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs5966709 8.02E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_022144 TNMD 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4828037 7.51E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_022144 TNMD 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs5921594 3.79E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_022150 NPVF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7791702 2.13E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_022150 NPVF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7791702 2.89E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_022150 NPVF 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Nonalcoholic Fatty Liver Disease rs17151904 1.00E-06 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_022154 SLC39A8 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs13107325 2.00E-13 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_022157 RRAGC 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs12131057 4.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_022160 DMRTA1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Waist Circumference rs613391 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_022160 DMRTA1 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Stomach Neoplasms rs10811771 8.00E-07 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_022160 DMRTA1 17478679 http://www.ncbi.nlm.nih.gov/pubmed/17478679 Myocardial Infarction rs10757278 1.00E-20 A common variant on chromosome 9p21 affects the risk of myocardial infarction. NHGRI|-1
NM_022160 DMRTA1 21606135 http://www.ncbi.nlm.nih.gov/pubmed/21606135 Coronary Artery Disease rs1333049 7.00E-58 A Genome-wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease. NHGRI|-1
NM_022160 DMRTA1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Coronary Disease rs1333049 1.00E-13 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_022160 DMRTA1 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs1333049 3.00E-19 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_022160 DMRTA1 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7020996 2.00E-07 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_022160 DMRTA1 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs2383208 2.00E-29 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_022160 DMRTA1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs10965250 1.00E-10 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_022160 DMRTA1 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs10811661 5.00E-06 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_022160 DMRTA1 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs10811661 5.00E-08 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_022160 DMRTA1 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs10811661 7.00E-07 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_022160 DMRTA1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs10811661 8.00E-15 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_022160 DMRTA1 21573907 http://www.ncbi.nlm.nih.gov/pubmed/21573907 "Diabetes Mellitus, Type 2" rs1333051 6.00E-10 "Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas." NHGRI|-1
NM_022160 DMRTA1 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Exploratory Behavior rs961831 7.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_022162 NOD2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs17221417 4.00E-11 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_022162 NOD2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11647841 5.50E-07 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_022162 NOD2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2066843 7.87E-13 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_022162 NOD2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs10521209 1.65E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_022162 NOD2 17447842 http://www.ncbi.nlm.nih.gov/pubmed/17447842 Crohn Disease rs5743289 1.00E-06 Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4. NHGRI|-1
NM_022162 NOD2 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn Disease rs5743289 6.00E-17 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_022162 NOD2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs5743289 4.65E-08 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_022162 NOD2 18758464 http://www.ncbi.nlm.nih.gov/pubmed/18758464 Inflammatory Bowel Diseases rs5743289 4.00E-10 Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. NHGRI|-1
NM_022162 NOD2 17684544 http://www.ncbi.nlm.nih.gov/pubmed/17684544 Crohn Disease rs2076756 1.00E-21 Systematic association mapping identifies NELL1 as a novel IBD disease gene. NHGRI|-1
NM_022162 NOD2 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs2076756 4.00E-69 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_022162 NOD2 17435756 http://www.ncbi.nlm.nih.gov/pubmed/17435756 Crohn Disease rs2076756 7.00E-14 Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. NHGRI|-1
NM_022162 NOD2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2076756 1.26E-14 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_022162 NOD2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2076756 5.00E-10 A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. NHGRI|-1
NM_022162 NOD2 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs2066847 2.00E-15 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_022162 NOD2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2066847 3.00E-24 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_022162 NOD2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9302752 1.45E-12 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_022162 NOD2 20018961 http://www.ncbi.nlm.nih.gov/pubmed/20018961 Leprosy rs9302752 4.00E-40 Genomewide association study of leprosy. NHGRI|-1
NM_022162 NOD2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs7194886 1.41E-07 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_022162 NOD2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs7194886 2.42E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_022163 MRPL46 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs894290 3.03E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_022166 XYLT1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8058794 9.05E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_022168 IFIH1 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs1990760 2.00E-11 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_022168 IFIH1 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs1990760 7.00E-09 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_022168 IFIH1 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs1990760 7.00E-10 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_022336 EDAR 20885792 http://www.ncbi.nlm.nih.gov/pubmed/20885792 Alzheimer Disease rs4676049 4.00E-08 Dementia revealed: novel chromosome 6 locus for late-onset Alzheimer disease provides genetic evidence for folate-pathway abnormalities. NHGRI|-1
NM_022337 RAB38 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17754282 4.30E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_022337 RAB38 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1386330 2.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_022349 MS4A6A 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs610932 2.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_022350 ERAP2 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs2549794 1.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_022355 DPEP2 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs255052 1.00E-07 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_022355 DPEP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs255052 2.36E-07 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_022357 DPEP3 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, HDL" rs255049 3.00E-08 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_022357 DPEP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs255049 3.06E-08 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_022361 POPDC3 21654844 http://www.ncbi.nlm.nih.gov/pubmed/21654844 Multiple Sclerosis rs11962089 8.00E-06 Genome-wide association study of severity in multiple sclerosis. NHGRI|-1
NM_022363 LHX5 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 C-Reactive Protein rs11066587 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_022365 DNAJC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2666781 6.29E-07 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_022365 DNAJC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2666781 9.68E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_022365 DNAJC1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2666781 2.89E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_022372 MLST8 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs26868 9.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_022373 HERPUD2 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs1362212 1.00E-13 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_022373 HERPUD2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs2392362 2.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_022373 HERPUD2 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Liver Cirrhosis rs343064 3.00E-08 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_022373 HERPUD2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs74992754 6.07E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_022377 ICAM4 18604267 http://www.ncbi.nlm.nih.gov/pubmed/18604267 Intercellular Adhesion Molecule-1 rs5498 5.00E-25 "Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women." NHGRI|-1
NM_022377 ICAM4 21533024 http://www.ncbi.nlm.nih.gov/pubmed/21533024 Intercellular Adhesion Molecule-1 rs5498 6.00E-89 "Genome-wide association analysis of soluble ICAM-1 concentration reveals novel associations at the NFKBIK, PNPLA3, RELA, and SH2B3 loci." NHGRI|-1
NM_022377 ICAM4 18604267 http://www.ncbi.nlm.nih.gov/pubmed/18604267 Intercellular Adhesion Molecule-1 rs281437 3.00E-10 "Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women." NHGRI|-1
NM_022377 ICAM4 20167578 http://www.ncbi.nlm.nih.gov/pubmed/20167578 Intercellular Adhesion Molecule-1 rs3093030 4.00E-23 Large-scale genomic studies reveal central role of ABO in sP-selectin and sICAM-1 levels. NHGRI|-1
NM_022405 SLC6A20 21572414 http://www.ncbi.nlm.nih.gov/pubmed/21572414 Metabolism rs17279437 3.00E-19 A genome-wide association study of metabolic traits in human urine. NHGRI|-1
NM_022436 ABCG5 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs6756629 3.00E-10 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_022436 ABCG5 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs6756629 2.00E-11 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_022436 ABCG5 17632509 http://www.ncbi.nlm.nih.gov/pubmed/17632509 Gallstones rs11887534 1.00E-14 A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. NHGRI|-1
NM_022437 ABCG8 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs6756629 3.00E-10 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_022437 ABCG8 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs6756629 2.00E-11 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_022437 ABCG8 17632509 http://www.ncbi.nlm.nih.gov/pubmed/17632509 Gallstones rs11887534 1.00E-14 A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. NHGRI|-1
NM_022437 ABCG8 20529992 http://www.ncbi.nlm.nih.gov/pubmed/20529992 Phytosterols rs41360247 6.00E-25 Genetic regulation of serum phytosterol levels and risk of coronary artery disease. NHGRI|-1
NM_022437 ABCG8 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs6544713 2.00E-20 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_022437 ABCG8 20529992 http://www.ncbi.nlm.nih.gov/pubmed/20529992 Phytosterols rs4245791 2.00E-50 Genetic regulation of serum phytosterol levels and risk of coronary artery disease. NHGRI|-1
NM_022443 MLF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1714524 1.36E-05 NBL-GWAS version 2 dbGaP|2895
NM_022443 MLF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1656377 4.94E-05 NBL-GWAS version 2 dbGaP|2895
NM_022444 SLC13A1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs2470984 8.97E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_022445 TPK1 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs10487524 9.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_022445 TPK1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1468375 1.41E-07 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_022454 SOX17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10089685 9.81E-05 NBL-GWAS version 2 dbGaP|2895
NM_022454 SOX17 20364137 http://www.ncbi.nlm.nih.gov/pubmed/20364137 Intracranial Aneurysm rs1504749 5.00E-07 Genome-wide association study of intracranial aneurysm identifies three new risk loci. NHGRI|-1
NM_022454 SOX17 18997786 http://www.ncbi.nlm.nih.gov/pubmed/18997786 Intracranial Aneurysm rs10958409 1.00E-10 Susceptibility loci for intracranial aneurysm in European and Japanese populations. NHGRI|-1
NM_022454 SOX17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs10958409 4.12E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_022459 XPO4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4770073 5.81E-07 NBL-GWAS version 2 dbGaP|2895
NM_022459 XPO4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9579975 6.22E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_022465 IKZF4 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs1701704 3.00E-08 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_022465 IKZF4 18198356 http://www.ncbi.nlm.nih.gov/pubmed/18198356 "Diabetes Mellitus, Type 1" rs1701704 9.00E-10 A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study. NHGRI|-1
NM_022467 CHST8 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs4805924 6.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_022475 HHIP 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1812175 1.00E-11 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_022475 HHIP 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs1812175 1.00E-09 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_022475 HHIP 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs1812175 4.00E-06 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_022475 HHIP 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs6854783 2.00E-09 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_022475 HHIP 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs1492820 1.00E-11 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_022475 HHIP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2353397 7.05E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_022479 WBSCR17 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11770998 4.73E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_022479 WBSCR17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11772787 1.56E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_022480 KLHL25 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Aging rs7176093 7.00E-06 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_022486 SUSD1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2782931 6.00E-06 Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_022552 DNMT3A 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs13428812 9.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_022556 GH2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2665838 5.00E-25 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_022557 GH2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2665838 5.00E-25 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_022558 GH2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2665838 5.00E-25 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_022566 MESDC1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2663944 1.34E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_022566 MESDC1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2683238 1.54E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_022566 MESDC1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1317060 3.89E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_022576 PDC 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs10911902 2.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_022640 CSH1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2665838 5.00E-25 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_022641 CSH1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2665838 5.00E-25 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_022648 TNS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs2571445 3.38E-04 Genome-wide association between genotype and incident heart failure in African-American participants dbGaP|2885
NM_022648 TNS1 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs2571445 1.00E-12 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_022650 RASA1 21173776 http://www.ncbi.nlm.nih.gov/pubmed/21173776 Personality rs2032794 2.00E-06 Meta-analysis of genome-wide association studies for personality. NHGRI|-1
NM_022659 EBF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4872354 5.99E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_022726 ELOVL4 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs346291 3.00E-07 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_022728 NEUROD6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1558477 2.58E-06 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_022728 NEUROD6 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs1558477 3.00E-07 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_022728 NEUROD6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7791986 8.41E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_022731 NUCKS1 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs823128 7.00E-08 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_022731 NUCKS1 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs12748961 4.00E-08 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_022740 HIPK2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs10954654 2.79E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_022743 SMYD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2275313 6.98E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_022743 SMYD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4654179 6.53E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_022743 SMYD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4654180 3.68E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_022743 SMYD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2105158 2.06E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_022746 MOSC1 21493818 http://www.ncbi.nlm.nih.gov/pubmed/21493818 Monocyte early outgrowth colony forming units rs6693017 3.00E-07 Genetic and clinical correlates of early-outgrowth colony-forming units. NHGRI|-1
NM_022746 MOSC1 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs12073837 2.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_022746 MOSC1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs11118620 7.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_022755 IPPK 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs9969804 8.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_022756 MEAF6 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Count rs9253 4.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_022758 C6orf106 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs2814993 4.00E-12 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_022767 AEN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2028389 2.41E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_022769 CRTC3 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs12915189 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_022771 TBC1D15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs328764 7.52E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_022772 EPS8L2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11246286 4.47E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_022779 DDX31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17149424 3.64E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_022782 MPHOSPH9 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs1790100 7.00E-07 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_022784 IQCH 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7359257 2.00E-06 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_022788 P2RY12 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs7637803 6.71E-06 NBL-GWAS version 1 dbGaP|2845
NM_022802 CTBP2 18264096 http://www.ncbi.nlm.nih.gov/pubmed/18264096 Prostatic Neoplasms rs4962416 2.00E-07 Multiple loci identified in a genome-wide association study of prostate cancer. NHGRI|-1
NM_022805 SNRPN 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Forced Expiratory Volume rs3867498 1.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_022806 SNRPN 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Forced Expiratory Volume rs3867498 1.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_022807 SNRPN 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Forced Expiratory Volume rs3867498 1.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_022808 SNRPN 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Forced Expiratory Volume rs3867498 1.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_022828 YTHDC2 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs17135859 8.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_022828 YTHDC2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs4621553 4.00E-08 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_022832 USP46 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Triglycerides rs346923 2.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_022840 METTL4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2644171 5.02E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_022840 METTL4 19727025 http://www.ncbi.nlm.nih.gov/pubmed/19727025 Exercise rs8097348 7.00E-06 Genome-wide association study of exercise behavior in Dutch and American adults. NHGRI|-1
NM_022840 METTL4 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs1879352 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_022840 METTL4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs770224 2.12E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_022843 PCDH20 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4886286 2.77E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_022843 PCDH20 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs3106598 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_022893 BCL11A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7593947 8.46E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_022893 BCL11A 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs1427407 6.00E-31 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_022893 BCL11A 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs766432 1.00E-10 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_022893 BCL11A 18245381 http://www.ncbi.nlm.nih.gov/pubmed/18245381 Fetal Hemoglobin rs11886868 7.00E-35 Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. NHGRI|-1
NM_022893 BCL11A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7592415 1.56E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_022893 BCL11A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17552189 8.46E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_022893 BCL11A 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs17552189 4.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_022893 BCL11A 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs991964 9.00E-06 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_022893 BCL11A 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs887912 2.00E-12 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_022893 BCL11A 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs10490113 5.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_022893 BCL11A 21493818 http://www.ncbi.nlm.nih.gov/pubmed/21493818 Monocyte early outgrowth colony forming units rs6712720 4.00E-06 Genetic and clinical correlates of early-outgrowth colony-forming units. NHGRI|-1
NM_022893 BCL11A 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs10202231 7.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_022893 BCL11A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs243023 1.13E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_022893 BCL11A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs243023 5.95E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_022893 BCL11A 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs243021 3.00E-15 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_022893 BCL11A 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs2540917 1.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_022894 PAPOLG 21037568 http://www.ncbi.nlm.nih.gov/pubmed/21037568 Hodgkin Disease rs1432295 2.00E-08 "A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)." NHGRI|-1
NM_022895 C12orf43 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs1169313 2.00E-10 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_022905 TTC23 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs7170952 1.25E-06 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_022906 STAG3L4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Body Mass Index rs10263639 3.04E-05 Genomewide association analysis of body mass index (BMI) in a birth cohort from a founder population dbGaP|2896
NM_022906 STAG3L4 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs10263639 3.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_022906 STAG3L4 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs6961611 7.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_022918 TMEM135 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1386330 2.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_022970 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11200014 9.14E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_022970 FGFR2 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs2981579 2.00E-10 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_022970 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2981579 4.36E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_022970 FGFR2 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs2981579 4.00E-31 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_022970 FGFR2 21060860 http://www.ncbi.nlm.nih.gov/pubmed/21060860 Breast Neoplasms rs2981575 1.00E-08 Common genetic variants and modification of penetrance of BRCA2-associated breast cancer. NHGRI|-1
NM_022970 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1219648 1.34E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_022970 FGFR2 17529973 http://www.ncbi.nlm.nih.gov/pubmed/17529973 Breast Neoplasms rs1219648 1.00E-10 A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. NHGRI|-1
NM_022970 FGFR2 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs1219648 1.00E-30 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_022970 FGFR2 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs1219648 2.00E-13 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_022970 FGFR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2420946 1.74E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_022970 FGFR2 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs2981582 2.00E-76 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_022970 FGFR2 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs2901286 4.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_022970 FGFR2 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs10788160 5.00E-15 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_023004 RTN4R 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs613930 8.67E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_023011 UPF3A 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7316983 1.05E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_023033 METTL1 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs703842 5.00E-11 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_023036 DNAI2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs7219585 1.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_023079 UBE2Z 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs46522 2.00E-08 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_023927 GRAMD3 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs1073203 9.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_023929 ZBTB10 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs272594 1.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_023929 ZBTB10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6992476 9.10E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_023935 DDRGK1 21659334 http://www.ncbi.nlm.nih.gov/pubmed/21659334 "Hepatitis C, Chronic" rs11697186 5.00E-17 Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C. NHGRI|-1
NM_023935 DDRGK1 21659334 http://www.ncbi.nlm.nih.gov/pubmed/21659334 "Hepatitis C, Chronic" rs11697186 9.00E-25 Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C. NHGRI|-1
NM_023935 DDRGK1 21659334 http://www.ncbi.nlm.nih.gov/pubmed/21659334 "Hepatitis C, Chronic" rs6139030 1.00E-15 Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C. NHGRI|-1
NM_023935 DDRGK1 21659334 http://www.ncbi.nlm.nih.gov/pubmed/21659334 "Hepatitis C, Chronic" rs6139030 2.00E-25 Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C. NHGRI|-1
NM_023942 LRRC61 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4721 5.03E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_023943 TMEM108 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs13072106 8.71E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_023943 TMEM108 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1197313 8.95E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_023943 TMEM108 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs6439371 1.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_023943 TMEM108 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs2369955 2.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_023948 MOSPD3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7786877 3.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_024006 VKORC1 19300499 http://www.ncbi.nlm.nih.gov/pubmed/19300499 Warfarin rs9923231 3.00E-181 "A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose." NHGRI|-1
NM_024006 VKORC1 20833655 http://www.ncbi.nlm.nih.gov/pubmed/20833655 Warfarin rs9923231 9.00E-31 Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. NHGRI|-1
NM_024007 EBF1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs7716011 6.15E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_024007 EBF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs202793 2.85E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_024007 EBF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs202793 7.42E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_024007 EBF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1145625 4.44E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_024007 EBF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2172745 4.65E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_024010 MTRR 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs2388004 6.00E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_024017 HOXB9 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs2326017 3.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_024021 MS4A4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1026250 1.20E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_024021 MS4A4A 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs1562990 4.00E-11 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_024021 MS4A4A 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs4938933 8.00E-12 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_024031 PRR14 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs7186852 3.00E-07 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_024031 PRR14 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs7197475 3.00E-08 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_024032 C17orf53 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs227584 9.00E-07 New sequence variants associated with bone mineral density. NHGRI|-1
NM_024034 GDAP1L1 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognition rs6017291 6.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_024043 DBNDD1 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs11648785 3.00E-09 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_024045 DDX50 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs2017305 9.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_024057 NUP37 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs2292303 8.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_024061 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Anthropometry rs7792939 5.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_024061 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weight rs7792939 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_024061 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weights and Measures rs7792939 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_024063 SPATA5L1 19430482 http://www.ncbi.nlm.nih.gov/pubmed/19430482 Creatinine rs2467853 6.00E-14 Multiple loci associated with indices of renal function and chronic kidney disease. NHGRI|-1
NM_024066 ERI3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17414912 5.93E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_024076 KCTD15 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs29941 3.00E-09 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_024076 KCTD15 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs29941 7.00E-12 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_024076 KCTD15 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs29941 5.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_024076 KCTD15 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs11084753 2.00E-08 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_024080 TRPM8 21666692 http://www.ncbi.nlm.nih.gov/pubmed/21666692 Migraine Disorders rs10166942 6.00E-12 Genome-wide association study reveals three susceptibility loci for common migraine in the general population. NHGRI|-1
NM_024081 PRRG4 19772629 http://www.ncbi.nlm.nih.gov/pubmed/19772629 Parkinson Disease rs10767971 5.00E-07 Genomewide association study for onset age in Parkinson disease. NHGRI|-1
NM_024086 METT10D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4268798 6.05E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_024086 METT10D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4268798 6.70E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_024086 METT10D 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, HDL" rs9891572 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_024086 METT10D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs9891572 2.33E-07 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_024090 ELOVL6 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs10011926 8.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_024101 MLPH 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs2292884 4.00E-08 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_024102 WDR77 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1264898 9.33E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_024102 WDR77 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1264897 1.01E-04 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_024108 TRAPPC6A 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 "Cholesterol, LDL" rs2159324 4.00E-07 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_024108 TRAPPC6A 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Cholesterol rs2159324 2.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_024113 C11orf49 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs7117404 9.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_024294 C6orf106 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs2814993 4.00E-12 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_024300 CHCHD7 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs9650315 4.00E-07 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_024300 CHCHD7 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs7815788 5.00E-06 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_024301 FKRP 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs11668878 4.00E-07 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_024306 FA2H 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs16948255 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_024310 PLEKHF1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs6509542 5.41E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_024322 CENPO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs41523444 1.63E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_024322 CENPO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs35213472 6.98E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_024323 C19orf57 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs7248982 6.56E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_024324 CRELD2 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs28372448 8.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_024330 SLC27A3 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs4434872 8.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_024335 IRX6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs17210989 1.49E-05 NBL-GWAS version 2 dbGaP|2895
NM_024335 IRX6 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs17291845 5.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_024336 IRX3 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs9921518 9.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_024337 IRX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs13359418 9.17E-05 NBL-GWAS version 2 dbGaP|2895
NM_024337 IRX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs16872251 9.48E-05 NBL-GWAS version 2 dbGaP|2895
NM_024337 IRX1 21107343 http://www.ncbi.nlm.nih.gov/pubmed/21107343 Myocardial Infarction rs11748327 5.00E-13 SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population. NHGRI|-1
NM_024337 IRX1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs7727102 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_024337 IRX1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10042985 8.53E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_024408 NOTCH2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs10923931 4.00E-08 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_024409 NPPC 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs749052 1.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_024409 NPPC 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2580816 6.00E-22 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_024411 PDYN 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs6136489 8.00E-11 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_024411 PDYN 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs6045676 3.00E-08 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_024415 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7730742 9.29E-05 NBL-GWAS version 2 dbGaP|2895
NM_024415 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10035707 5.09E-05 NBL-GWAS version 2 dbGaP|2895
NM_024415 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs957459 4.21E-05 NBL-GWAS version 2 dbGaP|2895
NM_024415 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2619046 1.76E-05 NBL-GWAS version 2 dbGaP|2895
NM_024415 DDX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs162096 3.33E-05 NBL-GWAS version 2 dbGaP|2895
NM_024420 PLA2G4A 18471798 http://www.ncbi.nlm.nih.gov/pubmed/18471798 "Osteoarthritis, Knee" rs4140564 3.00E-06 Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis. NHGRI|-1
NM_024423 DSC3 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Parathyroid Hormone rs2729409 3.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_024424 WT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs11031676 5.68E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_024424 WT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7944342 6.98E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_024426 WT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs11031676 5.68E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_024426 WT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7944342 6.98E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_024429 PRKAG2 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs7805747 4.00E-12 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_024429 PRKAG2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs10224002 3.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_024429 PRKAG2 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs10224002 6.00E-15 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_024429 PRKAG2 21305692 http://www.ncbi.nlm.nih.gov/pubmed/21305692 Bipolar Disorder rs7795096 2.00E-06 Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder. NHGRI|-1
NM_024430 PSTPIP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4890614 6.88E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_024490 ATP10A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12901627 2.22E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_024490 ATP10A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12717755 1.35E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_024490 ATP10A 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs17636733 2.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_024490 ATP10A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2930629 5.39E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_024496 C14orf4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs17105232 1.50E-05 NBL-GWAS version 2 dbGaP|2895
NM_024501 HOXD1 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs2072590 5.00E-14 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_024504 PRDM14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6472491 3.15E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_024513 FYCO1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2133660 8.02E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_024514 CYP2R1 20541252 http://www.ncbi.nlm.nih.gov/pubmed/20541252 Vitamin D rs10741657 3.00E-20 Common genetic determinants of vitamin D insufficiency: a genome-wide association study. NHGRI|-1
NM_024520 C2orf47 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs1569175 9.00E-07 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_024520 C2orf47 19727025 http://www.ncbi.nlm.nih.gov/pubmed/19727025 Exercise rs12612420 8.00E-06 Genome-wide association study of exercise behavior in Dutch and American adults. NHGRI|-1
NM_024526 EPS8L3 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs10494112 7.00E-35 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_024526 EPS8L3 20436471 http://www.ncbi.nlm.nih.gov/pubmed/20436471 Osteitis Deformans rs484959 5.00E-24 "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone." NHGRI|-1
NM_024526 EPS8L3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs525566 5.88E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_024552 LASS4 19798445 http://www.ncbi.nlm.nih.gov/pubmed/19798445 Sphingomyelins rs7258249 2.00E-27 Genetic determinants of circulating sphingolipid concentrations in European populations. NHGRI|-1
NM_024554 PGBD5 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs701157 4.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_024557 RIC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4758051 2.83E-08 NBL-GWAS version 2 dbGaP|2895
NM_024557 RIC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10840002 6.01E-06 NBL-GWAS version 2 dbGaP|2895
NM_024569 MPZL1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs12757250 9.23E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_024570 RNASEH2B 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2408213 5.24E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_024576 OGFRL1 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs11968814 9.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_024580 EFTUD1 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs12324805 7.00E-06 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_024582 FAT4 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1395241 8.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_024582 FAT4 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs12639834 6.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_024582 FAT4 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs950063 9.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_024582 FAT4 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Ankle Brachial Index rs1320267 7.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_024582 FAT4 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs1986655 2.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_024584 CCDC121 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs3749147 1.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_024590 ARSJ 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs13134836 2.84E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_024590 ARSJ 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12331375 1.11E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_024593 EFCAB1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs12155623 3.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_024593 EFCAB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900238 9.63E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_024596 MCPH1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Attention Deficit Disorder with Hyperactivity rs4875598 9.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_024596 MCPH1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7817815 4.96E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_024604 RPAP3 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs11610206 3.00E-07 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_024605 ARHGAP10 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs6845865 7.00E-07 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_024607 PPP1R3B 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs9987289 3.00E-13 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_024607 PPP1R3B 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs9987289 1.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_024607 PPP1R3B 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs9987289 4.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_024607 PPP1R3B 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs6601299 1.00E-08 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_024607 PPP1R3B 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs2126259 7.00E-12 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_024607 PPP1R3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9329191 6.16E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_024607 PPP1R3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12334460 2.92E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_024613 PLEKHF2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17668689 9.85E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_024613 PLEKHF2 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs4392868 8.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_024613 PLEKHF2 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs7000734 4.00E-07 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_024615 PARP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13157992 9.03E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_024615 PARP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7720960 7.28E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_024615 PARP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7378969 6.04E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_024615 PARP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1016620 9.80E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_024619 FN3KRP 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1046896 2.00E-26 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_024621 VEPH1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs9866141 9.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_024623 OGFOD2 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs7296418 2.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_024626 VTCN1 19116933 http://www.ncbi.nlm.nih.gov/pubmed/19116933 "Arthritis, Juvenile Rheumatoid" rs12046117 1.00E-06 Identification of a novel susceptibility locus for juvenile idiopathic arthritis by genome-wide association analysis. NHGRI|-1
NM_024630 ZDHHC14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9365242 6.70E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_024630 ZDHHC14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9365243 4.53E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_024630 ZDHHC14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6903041 1.19E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_024635 NAA35 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7048878 9.89E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_024639 ZNF322A 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9379897 1.45E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_024645 ZMAT4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2122950 2.02E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_024645 ZMAT4 17903298 http://www.ncbi.nlm.nih.gov/pubmed/17903298 Blood Glucose rs2722425 2.00E-08 Genome-wide association with diabetes-related traits in the Framingham Heart Study. NHGRI|-1
NM_024645 ZMAT4 17903298 http://www.ncbi.nlm.nih.gov/pubmed/17903298 Blood Glucose rs2722425 9.00E-06 Genome-wide association with diabetes-related traits in the Framingham Heart Study. NHGRI|-1
NM_024645 ZMAT4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4736788 4.88E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_024645 ZMAT4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10094981 4.82E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_024645 ZMAT4 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs11786458 9.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_024665 TBL1XR1 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs6772209 3.00E-07 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_024665 TBL1XR1 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs6799767 4.00E-07 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_024669 ANKRD55 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs415407 4.00E-09 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_024669 ANKRD55 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs6859219 1.00E-11 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_024675 PALB2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Bipolar Disorder rs420259 6.00E-08 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_024680 E2F8 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs12146588 8.75E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_024686 TTLL7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10437024 2.02E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_024686 TTLL7 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs11163585 9.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_024686 TTLL7 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Tumor Necrosis Factor-alpha rs7552393 5.00E-07 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_024686 TTLL7 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs7539409 1.00E-06 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_024697 ZNF385D 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs3821396 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_024697 ZNF385D 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs1490157 5.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_024697 ZNF385D 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs11719664 2.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_024697 ZNF385D 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs2593321 8.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_024704 KIF16B 21139019 http://www.ncbi.nlm.nih.gov/pubmed/21139019 Carcinoid Tumor rs2208059 4.00E-07 A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum. NHGRI|-1
NM_024709 C1orf115 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Amyotrophic Lateral Sclerosis rs337161 3.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_024717 MCTP1 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs17418283 1.00E-07 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_024722 ACBD4 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs12946454 1.00E-08 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_024722 ACBD4 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs4986172 2.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_024730 RERGL 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs9971637 2.00E-06 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_024731 KLHL36 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs11647936 4.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_024734 CLMN 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs1187614 2.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_024734 CLMN 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs8014194 2.00E-08 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_024741 ZNF408 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7932354 4.00E-09 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_024751 GSTCD 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs10516526 2.00E-23 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_024755 SLTM 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs7179456 7.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_024757 EHMT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10780192 4.80E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_024761 MOBKL2B 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 "Arthritis, Rheumatoid" rs7046653 5.00E-07 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_024766 C2orf34 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs17498753 6.93E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_024769 ASAM 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs735665 4.00E-12 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NM_024769 ASAM 20639881 http://www.ncbi.nlm.nih.gov/pubmed/20639881 "Lymphoma, Follicular" rs735665 4.00E-09 Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. NHGRI|-1
NM_024769 ASAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11219172 5.56E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_024769 ASAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4936819 1.24E-06 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_024782 NHEJ1 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs6724465 2.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_024782 NHEJ1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs16859517 5.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_024782 NHEJ1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1052483 1.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_024817 THSD4 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs12899618 7.00E-15 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_024817 THSD4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7181587 1.25E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_024820 DENND1A 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Personality rs7852296 9.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_024820 DENND1A 21151128 http://www.ncbi.nlm.nih.gov/pubmed/21151128 Polycystic Ovary Syndrome rs10818854 9.00E-18 "Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3." NHGRI|-1
NM_024820 DENND1A 21151128 http://www.ncbi.nlm.nih.gov/pubmed/21151128 Polycystic Ovary Syndrome rs2479106 8.00E-19 "Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3." NHGRI|-1
NM_024821 CCDC134 21123754 http://www.ncbi.nlm.nih.gov/pubmed/21123754 Alzheimer Disease rs7364180 1.00E-06 "Genome-wide association study of CSF biomarkers Abeta1-42, t-tau, and p-tau181p in the ADNI cohort." NHGRI|-1
NM_024828 C9orf82 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10453196 3.37E-06 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_024828 C9orf82 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10491819 5.58E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_024828 C9orf82 19483685 http://www.ncbi.nlm.nih.gov/pubmed/19483685 Drug-Induced Liver Injury rs10812428 1.00E-06 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. NHGRI|-1
NM_024828 C9orf82 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12236180 4.63E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_024828 C9orf82 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs1889899 6.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_024829 PLBD1 20543847 http://www.ncbi.nlm.nih.gov/pubmed/20543847 Testicular Neoplasms rs2900333 6.00E-10 "Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer." NHGRI|-1
NM_024830 LPCAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4608970 2.35E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_024830 LPCAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4608970 8.48E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_024830 LPCAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4551123 4.31E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_024832 RIN3 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs10498635 3.00E-11 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_024832 RIN3 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs4904947 8.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_024838 THNSL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10508687 8.45E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_024841 PRR5L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2292648 9.25E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_024867 SPEF2 21244703 http://www.ncbi.nlm.nih.gov/pubmed/21244703 Multiple Sclerosis rs931555 4.00E-07 Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data. NHGRI|-1
NM_024867 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286411 2.12E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_024867 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 5.38E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_024867 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 6.67E-07 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_024867 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs169587 1.61E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_024867 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1605683 1.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_024867 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286388 1.39E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_024867 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 1.29E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_024867 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 3.17E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_024870 PREX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7839608 5.83E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_024870 PREX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1369165 5.48E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_024870 PREX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs874805 8.67E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_024893 TMEM90B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1883924 4.31E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_024893 TMEM90B 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs6049375 8.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_024895 PDZD7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs701837 1.19E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_024896 ERMP1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs10815285 1.96E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_024896 ERMP1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs17571216 4.47E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_024911 WLS 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs187922 2.61E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_024911 WLS 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1430742 3.00E-13 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_024911 WLS 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2566755 2.00E-12 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_024921 POF1B 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs12557215 5.67E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_024923 NUP210 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs444944 1.30E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_024928 OBFC1 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 Brachial Artery rs3814219 9.00E-07 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_024928 OBFC1 20421499 http://www.ncbi.nlm.nih.gov/pubmed/20421499 Telomere rs4387287 2.00E-11 Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. NHGRI|-1
NM_024928 OBFC1 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs7913069 9.00E-14 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_024948 FAM188A 19151714 http://www.ncbi.nlm.nih.gov/pubmed/19151714 Obesity rs10508503 2.00E-07 Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. NHGRI|-1
NM_024949 WWC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs11132168 6.29E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_024953 NAA25 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs17696736 2.00E-14 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_024953 NAA25 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs17696736 2.00E-16 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_024953 NAA25 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs17696736 6.00E-18 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_024953 NAA25 21437268 http://www.ncbi.nlm.nih.gov/pubmed/21437268 Head and Neck Neoplasms rs4767364 2.00E-08 A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. NHGRI|-1
NM_024958 NRSN2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs6051520 2.00E-07 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_024966 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs12594515 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_024966 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs12594515 7.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_024966 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4603502 3.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_024966 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1865648 1.57E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_024966 SEMA6D 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11857760 6.14E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_024969 CSRNP3 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs6710518 5.00E-10 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_024971 TRPM3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4745062 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_024971 TRPM3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12350232 8.34E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_024993 LRRTM4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1921246 5.63E-06 NBL-GWAS version 1 dbGaP|2845
NM_024993 LRRTM4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs17012789 4.44E-06 NBL-GWAS version 1 dbGaP|2845
NM_024997 ATF7IP2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs13335336 7.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_025003 ADAMTS20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7310342 3.21E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_025047 ARL14 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs4679904 1.00E-06 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_025052 YSK4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6754977 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_025059 C6orf97 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs4870044 2.00E-11 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_025059 C6orf97 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs4870044 2.00E-07 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_025059 C6orf97 21540461 http://www.ncbi.nlm.nih.gov/pubmed/21540461 "Leukemia, Myeloid, Chronic-Phase" rs4869742 2.00E-06 A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia. NHGRI|-1
NM_025059 C6orf97 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs3757318 3.00E-06 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_025059 C6orf97 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs1038304 4.00E-10 New sequence variants associated with bone mineral density. NHGRI|-1
NM_025059 C6orf97 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs1038304 4.00E-11 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_025059 C6orf97 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs1038304 5.00E-09 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_025059 C6orf97 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs6929137 2.00E-10 New sequence variants associated with bone mineral density. NHGRI|-1
NM_025059 C6orf97 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs3734805 1.00E-07 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_025059 C6orf97 19219042 http://www.ncbi.nlm.nih.gov/pubmed/19219042 Breast Neoplasms rs2046210 2.00E-15 Genome-wide association study identifies a new breast cancer susceptibility locus at 6q25.1. NHGRI|-1
NM_025069 ZNF703 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs11785595 5.22E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_025074 FRAS1 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs1268789 7.00E-08 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_025090 USP36 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7218605 3.56E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_025107 MYCT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs633596 5.06E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_025124 TMEM134 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7124630 4.90E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_025130 HKDC1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2279927 6.05E-06 NBL-GWAS version 1 dbGaP|2845
NM_025134 CHD9 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12444248 3.90E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_025134 CHD9 17529967 http://www.ncbi.nlm.nih.gov/pubmed/17529967 Breast Neoplasms rs3803662 1.00E-36 Genome-wide association study identifies novel breast cancer susceptibility loci. NHGRI|-1
NM_025134 CHD9 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs3803662 1.00E-09 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_025134 CHD9 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs3803662 3.00E-15 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_025134 CHD9 20872241 http://www.ncbi.nlm.nih.gov/pubmed/20872241 Breast Neoplasms rs3803662 4.00E-07 A combined analysis of genome-wide association studies in breast cancer. NHGRI|-1
NM_025134 CHD9 17529974 http://www.ncbi.nlm.nih.gov/pubmed/17529974 Breast Neoplasms rs3803662 6.00E-19 Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancer. NHGRI|-1
NM_025134 CHD9 20585626 http://www.ncbi.nlm.nih.gov/pubmed/20585626 Breast Neoplasms rs4784227 1.00E-28 Identification of a functional genetic variant at 16q12.1 for breast cancer risk: results from the Asia Breast Cancer Consortium. NHGRI|-1
NM_025134 CHD9 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast Neoplasms rs3112612 4.00E-10 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_025134 CHD9 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3104807 1.01E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_025135 FHOD3 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs17651157 1.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_025142 TAOK1 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs2138852 1.00E-22 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_025142 TAOK1 19110211 http://www.ncbi.nlm.nih.gov/pubmed/19110211 Platelet Count rs2138852 7.00E-28 A genome-wide association study identifies three loci associated with mean platelet volume. NHGRI|-1
NM_025144 ALPK1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs7658978 3.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_025145 C10orf79 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs515910 4.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_025152 NUBPL 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs7142881 2.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_025152 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs8016004 3.64E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_025152 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2151784 3.65E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_025152 NUBPL 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2039485 6.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_025152 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6571481 1.55E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_025152 NUBPL 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs915071 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_025152 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs915071 4.18E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_025152 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs972396 7.82E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_025152 NUBPL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1952966 4.84E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_025153 ATP10B 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs2431697 2.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_025153 ATP10B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs883517 5.94E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_025153 ATP10B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12514981 7.68E-05 NBL-GWAS version 2 dbGaP|2895
NM_025158 RUFY1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4701136 1.95E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_025164 SIK3 21149283 http://www.ncbi.nlm.nih.gov/pubmed/21149283 "Receptors, Transferrin" rs10047462 4.00E-25 Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. NHGRI|-1
NM_025164 SIK3 18193046 http://www.ncbi.nlm.nih.gov/pubmed/18193046 Triglycerides rs2075292 5.00E-08 Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. NHGRI|-1
NM_025170 PREX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7839608 5.83E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_025170 PREX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1369165 5.48E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_025170 PREX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs874805 8.67E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_025179 PLXNA2 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs17259784 6.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_025179 PLXNA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12145940 4.93E-05 NBL-GWAS version 2 dbGaP|2895
NM_025179 PLXNA2 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs2745967 7.00E-08 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_025180 CEP63 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs10935120 7.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_025182 KIAA1539 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs10972341 9.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_025195 TRIB1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs2954021 1.00E-07 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_025195 TRIB1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs2954026 8.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_025195 TRIB1 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs17321515 4.00E-17 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_025195 TRIB1 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs17321515 7.00E-13 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_025195 TRIB1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs2954029 2.00E-11 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_025195 TRIB1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs2954029 3.00E-19 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_025195 TRIB1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2954033 9.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_025195 TRIB1 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs6987702 3.00E-06 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_025195 TRIB1 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs6987702 3.00E-09 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_025195 TRIB1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs2954038 7.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_025195 TRIB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7012891 8.45E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_025195 TRIB1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs1551398 5.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_025201 PLEKHO2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs12595292 9.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_025208 PDGFD 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs10895547 3.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_025208 PDGFD 21118971 http://www.ncbi.nlm.nih.gov/pubmed/21118971 Small Cell Lung Carcinoma rs716274 9.00E-08 Genome-wide interrogation identifies YAP1 variants associated with survival of small-cell lung cancer patients. NHGRI|-1
NM_025208 PDGFD 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs1917445 6.00E-07 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_025208 PDGFD 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs974819 2.00E-09 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_025216 WNT10A 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs7349332 1.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_025216 WNT10A 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair rs7349332 3.00E-14 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_025218 ULBP1 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs1853665 7.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_025221 KCNIP4 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4697177 6.80E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_025221 KCNIP4 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs6825103 2.13E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_025221 KCNIP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs876477 5.40E-06 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_025221 KCNIP4 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs358592 3.00E-06 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_025221 KCNIP4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4697227 1.84E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_025225 PNPLA3 21423719 http://www.ncbi.nlm.nih.gov/pubmed/21423719 Non-alcoholic Fatty Liver Disease [Supplementary Concept] rs738409 4.00E-34 Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. NHGRI|-1
NM_025225 PNPLA3 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs2281135 8.00E-16 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_025236 RNF39 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs9261290 1.73E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_025236 RNF39 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4711209 1.03E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_025236 RNF39 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs916570 1.10E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_025237 SOST 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs1513670 2.00E-08 New sequence variants associated with bone mineral density. NHGRI|-1
NM_025238 BTBD1 21326860 http://www.ncbi.nlm.nih.gov/pubmed/21326860 Mucocutaneous Lymph Node Syndrome rs1568657 7.00E-06 Identification of novel susceptibility Loci for kawasaki disease in a han chinese population by a genome-wide association study. NHGRI|-1
NM_025239 PDCD1LG2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs4740820 6.41E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_025240 CD276 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs1038094 9.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_025245 PBX4 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs16996148 3.00E-08 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_025245 PBX4 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs16996148 3.00E-09 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_025245 PBX4 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs16996148 4.00E-09 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_025245 PBX4 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs17216525 4.00E-11 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_025247 ACAD10 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs11066015 7.00E-21 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_025248 SRCIN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3892952 1.19E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_025256 EHMT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs652888 1.56E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_025256 EHMT2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs652888 6.12E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_025256 EHMT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs652888 4.73E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_025256 EHMT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7743807 8.09E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_025256 EHMT2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs486416 8.91E-14 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_025256 EHMT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs535586 1.21E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_025256 EHMT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs659445 1.45E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_025257 SLC44A4 20526339 http://www.ncbi.nlm.nih.gov/pubmed/20526339 Vitiligo rs11966200 1.00E-48 Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. NHGRI|-1
NM_025257 SLC44A4 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs494620 5.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_025257 SLC44A4 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2736428 1.00E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_025257 SLC44A4 20421499 http://www.ncbi.nlm.nih.gov/pubmed/20421499 Telomere rs2736428 3.00E-06 Genome-wide association identifies OBFC1 as a locus involved in human leukocyte telomere biology. NHGRI|-1
NM_025257 SLC44A4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs9267658 2.51E-84 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_025258 C6orf27 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs707928 8.89E-111 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_025258 C6orf27 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs707928 3.39E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_025259 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3749953 2.36E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_025259 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3131379 7.24E-85 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_025259 MSH5 18204446 http://www.ncbi.nlm.nih.gov/pubmed/18204446 "Lupus Erythematosus, Systemic" rs3131379 2.00E-52 "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci." NHGRI|-1
NM_025259 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3131379 4.89E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_025261 LY6G6C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs805294 5.69E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_025262 LY6G5C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2280800 4.75E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_025264 THUMPD2 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs2716734 2.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_025264 THUMPD2 18957941 http://www.ncbi.nlm.nih.gov/pubmed/18957941 Personality rs2540226 3.00E-06 Genome-wide association scan for five major dimensions of personality. NHGRI|-1
NM_025265 TSEN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs9833097 6.72E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_030569 ITIH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs4748940 3.09E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_030571 NDFIP1 20543847 http://www.ncbi.nlm.nih.gov/pubmed/20543847 Testicular Neoplasms rs4624820 1.00E-14 "Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer." NHGRI|-1
NM_030571 NDFIP1 19483681 http://www.ncbi.nlm.nih.gov/pubmed/19483681 Testicular Neoplasms rs4624820 3.00E-13 A genome-wide association study of testicular germ cell tumor. NHGRI|-1
NM_030571 NDFIP1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs11167764 2.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_030579 CYB5B 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1364063 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_030581 WDR59 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs16948255 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_030582 COL18A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs957795 1.25E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_030582 COL18A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs957794 1.01E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_030589 CYP2A7 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs4105144 2.00E-12 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_030594 CPEB1 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs783540 4.00E-06 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_030621 DICER1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11624318 7.62E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_030621 DICER1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11160219 3.45E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_030621 DICER1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8007115 4.06E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_030621 DICER1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs8019257 8.50E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_030623 SPHKAP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4438469 3.55E-05 NBL-GWAS version 2 dbGaP|2895
NM_030623 SPHKAP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6760875 2.73E-05 NBL-GWAS version 2 dbGaP|2895
NM_030623 SPHKAP 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs10200894 1.90E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_030627 CPEB4 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6861681 2.00E-09 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_030627 CPEB4 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs359457 3.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_030632 ASXL3 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs1013696 4.00E-06 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_030636 EEPD1 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4302748 5.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_030637 DDHD1 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs1380131 9.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_030643 APOL4 20532800 http://www.ncbi.nlm.nih.gov/pubmed/20532800 "Kidney Failure, Chronic" rs4821469 2.00E-19 Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA. NHGRI|-1
NM_030648 SETD7 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs17050782 8.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_030650 KIAA1715 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs847126 6.56E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_030651 PRRT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7383258 1.51E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_030651 PRRT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9296009 1.19E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_030652 PPT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3134603 3.36E-116 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_030652 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3096697 2.16E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_030652 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3096697 5.66E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_030652 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130347 1.22E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_030652 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130347 3.62E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_030664 PTER 19151714 http://www.ncbi.nlm.nih.gov/pubmed/19151714 Obesity rs10508503 2.00E-07 Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. NHGRI|-1
NM_030665 RAI1 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs11868035 6.00E-08 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_030665 RAI1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs12936587 4.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_030674 SLC38A1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs1373549 8.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_030751 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2839658 1.84E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_030751 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2839658 8.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_030751 ZEB1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12217563 3.40E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_030751 ZEB1 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_030753 WNT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs415430 4.50E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_030753 WNT3 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs2074404 1.00E-06 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_030753 WNT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs2074404 9.79E-04 Genome-wide association between genotype and incident myocardial infarction in African-American participants dbGaP|2883
NM_030754 SAA2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs12282742 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_030755 TMX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2884058 2.85E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_030755 TMX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11157816 7.91E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_030756 TCF7L2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7901695 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_030756 TCF7L2 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs7901695 1.00E-48 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_030756 TCF7L2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs4506565 5.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_030756 TCF7L2 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4506565 1.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_030756 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.25E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_030756 TCF7L2 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs7903146 1.00E-30 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_030756 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7903146 1.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_030756 TCF7L2 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs7903146 2.00E-10 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_030756 TCF7L2 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs7903146 2.00E-31 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_030756 TCF7L2 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs7903146 2.00E-34 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_030756 TCF7L2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7903146 2.00E-51 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_030756 TCF7L2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs7903146 3.00E-23 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_030756 TCF7L2 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs7903146 5.00E-08 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_030756 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 6.00E-16 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_030756 TCF7L2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Diabetes Mellitus, Type 2" rs7903146 7.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_030756 TCF7L2 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs7903146 8.00E-12 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_030756 TCF7L2 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs7903146 9.00E-30 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_030756 TCF7L2 20849430 http://www.ncbi.nlm.nih.gov/pubmed/20849430 "Hemoglobin A, Glycosylated" rs7903146 1.00E-07 The TCF7L2 diabetes risk variant is associated with HbAG??(C) levels: a genome-wide association meta-analysis. NHGRI|-1
NM_030756 TCF7L2 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs12243326 1.00E-07 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_030756 TCF7L2 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12255372 1.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_030758 OSBP2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs5753271 4.35E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_030761 WNT4 20601957 http://www.ncbi.nlm.nih.gov/pubmed/20601957 Endometriosis rs16826658 2.00E-06 A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese. NHGRI|-1
NM_030761 WNT4 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs7521902 5.00E-06 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_030761 WNT4 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs7524102 1.00E-16 New sequence variants associated with bone mineral density. NHGRI|-1
NM_030761 WNT4 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs7524102 1.00E-06 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_030761 WNT4 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7524102 3.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_030761 WNT4 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs7524102 5.00E-16 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_030761 WNT4 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs7524102 9.00E-07 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_030761 WNT4 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs7524102 9.00E-09 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_030761 WNT4 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs7524102 2.00E-13 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_030761 WNT4 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs7524102 3.00E-07 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_030761 WNT4 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs6696981 2.00E-08 New sequence variants associated with bone mineral density. NHGRI|-1
NM_030761 WNT4 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs6426749 9.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_030776 ZBP1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs2073145 2.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_030777 SLC2A10 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Body Fat Distribution rs6066084 2.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_030782 CLPTM1L 18978790 http://www.ncbi.nlm.nih.gov/pubmed/18978790 Lung Neoplasms rs402710 4.00E-06 Lung cancer susceptibility locus at 5p15.33. NHGRI|-1
NM_030782 CLPTM1L 18978787 http://www.ncbi.nlm.nih.gov/pubmed/18978787 Lung Neoplasms rs401681 8.00E-09 Common 5p15.33 and 6p21.33 variants influence lung cancer risk. NHGRI|-1
NM_030782 CLPTM1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs401681 3.66E-07 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_030782 CLPTM1L 20101243 http://www.ncbi.nlm.nih.gov/pubmed/20101243 Pancreatic Neoplasms rs401681 7.00E-07 "A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33." NHGRI|-1
NM_030782 CLPTM1L 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs401681 1.00E-10 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_030782 CLPTM1L 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs401681 5.00E-07 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_030782 CLPTM1L 19836008 http://www.ncbi.nlm.nih.gov/pubmed/19836008 Lung Neoplasms rs31489 2.00E-10 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. NHGRI|-1
NM_030782 CLPTM1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs31489 1.64E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_030782 CLPTM1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4635969 1.05E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_030782 CLPTM1L 20543847 http://www.ncbi.nlm.nih.gov/pubmed/20543847 Testicular Neoplasms rs4635969 1.00E-23 "Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer." NHGRI|-1
NM_030782 CLPTM1L 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs4975616 3.00E-09 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_030782 CLPTM1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4975616 8.29E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_030785 RSPH6A 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs8111071 4.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12731209 1.30E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12731209 3.35E-08 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1759016 2.07E-09 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1759016 4.71E-07 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922152 2.63E-17 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922152 5.21E-12 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922153 2.63E-17 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10922153 5.21E-12 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6663083 2.70E-17 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6663083 5.47E-12 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7555070 5.60E-22 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7555070 5.69E-24 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1332666 1.19E-50 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1332666 3.74E-45 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7531555 4.87E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6667243 1.13E-57 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_030787 CFHR5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6667243 3.34E-66 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_030788 TM7SF4 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs2458413 7.00E-17 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_030797 FAM49A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2042079 3.40E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_030803 ATG16L1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs10210302 5.00E-14 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_030803 ATG16L1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs3828309 2.00E-32 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_030803 ATG16L1 17435756 http://www.ncbi.nlm.nih.gov/pubmed/17435756 Crohn Disease rs2241880 1.00E-13 Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. NHGRI|-1
NM_030803 ATG16L1 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs2241880 3.00E-06 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_030803 ATG16L1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2241880 4.40E-08 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_030803 ATG16L1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs3792109 7.00E-41 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_030803 ATG16L1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs3792106 2.31E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_030803 ATG16L1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs10933436 7.00E-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_030805 LMAN2L 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs2314398 3.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_030812 ACTL8 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs16861326 2.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_030819 GFOD2 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs12449157 2.00E-07 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_030820 COL21A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12663282 4.56E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_030820 COL21A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9475671 1.07E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_030821 PLA2G12A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2285714 3.58E-07 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_030821 PLA2G12A 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs2285714 3.00E-07 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_030821 PLA2G12A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2285714 7.85E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_030821 PLA2G12A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7439493 1.26E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_030821 PLA2G12A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7439493 1.59E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_030821 PLA2G12A 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs10033900 4.00E-10 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_030821 PLA2G12A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10033900 6.35E-07 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_030821 PLA2G12A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10033900 6.70E-07 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_030821 PLA2G12A 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs10033900 9.00E-09 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_030877 CTNNBL1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Bone Density rs4811196 1.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_030882 APOL2 20532800 http://www.ncbi.nlm.nih.gov/pubmed/20532800 "Kidney Failure, Chronic" rs4821469 2.00E-19 Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA. NHGRI|-1
NM_030883 OR2H1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2746150 3.42E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_030893 CD1E 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1065457 6.43E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_030899 ZNF323 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs853679 2.52E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_030899 ZNF323 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs853676 5.22E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_030899 ZNF323 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs853676 6.14E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_030906 STK33 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs10769908 1.00E-06 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_030906 STK33 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs4929949 3.00E-09 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_030915 LBH 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs7579944 1.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_030923 TMEM163 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs6710823 7.00E-09 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_030925 CAB39L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7328100 8.21E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_030928 CDT1 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs837763 4.00E-13 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_030932 DIAPH3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs7336489 8.33E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_030932 DIAPH3 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs10492604 4.00E-06 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_030932 DIAPH3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7988007 6.28E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_030932 DIAPH3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs9538078 7.05E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_030932 DIAPH3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1330748 1.01E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_030932 DIAPH3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs1537473 7.53E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_030932 DIAPH3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs9569918 7.11E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_030932 DIAPH3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12428128 1.19E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_030932 DIAPH3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12428128 2.02E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_030939 C6orf62 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs17419851 9.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_030943 AMN 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs10133111 5.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_030945 C1QTNF3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10075914 7.33E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_030945 C1QTNF3 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs409045 8.00E-07 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NM_030948 PHACTR1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs1332844 6.00E-08 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_030948 PHACTR1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs9349379 9.00E-26 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_030948 PHACTR1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs12526453 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_030948 PHACTR1 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs12526453 1.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_030948 PHACTR1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs4715166 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_030955 ADAMTS12 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs6868223 2.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_030956 TLR10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6838905 6.46E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_030956 TLR10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6838905 7.66E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_030956 TLR10 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7658334 1.49E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_030957 ADAMTS10 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs7249094 1.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_030958 SLCO5A1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs16936455 7.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_030958 SLCO5A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6472491 3.15E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_030959 OR12D3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3749971 8.06E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_030960 SPACA1 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs2509458 7.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_030960 SPACA1 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 "Ventricular Function, Left" rs366676 2.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_030963 RNF146 18326623 http://www.ncbi.nlm.nih.gov/pubmed/18326623 Breast Neoplasms rs2180341 3.00E-08 Genome-wide association study provides evidence for a breast cancer risk locus at 6q22.33. NHGRI|-1
NM_030964 SPRY4 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs17577085 4.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_030964 SPRY4 20543847 http://www.ncbi.nlm.nih.gov/pubmed/20543847 Testicular Neoplasms rs4624820 1.00E-14 "Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer." NHGRI|-1
NM_030964 SPRY4 19483681 http://www.ncbi.nlm.nih.gov/pubmed/19483681 Testicular Neoplasms rs4624820 3.00E-13 A genome-wide association study of testicular germ cell tumor. NHGRI|-1
NM_030965 ST6GALNAC5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs664576 8.58E-05 NBL-GWAS version 2 dbGaP|2895
NM_031207 HYI 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12069733 8.59E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_031218 ZNF93 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs10411195 6.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_031226 CYP19A1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs2305707 7.00E-07 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_031277 RNF17 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1158061 2.59E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_031277 RNF17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9511451 6.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_031277 RNF17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9511479 8.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_031277 RNF17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7335910 2.69E-06 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_031279 AGXT2L1 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs4956211 1.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_031281 FCRL5 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs6427356 8.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_031296 RAB33B 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs17050782 8.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_031303 KATNAL2 21173776 http://www.ncbi.nlm.nih.gov/pubmed/21173776 Personality rs2576037 1.00E-07 Meta-analysis of genome-wide association studies for personality. NHGRI|-1
NM_031305 ARHGAP24 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs7692808 6.00E-20 Genome-wide association study of PR interval. NHGRI|-1
NM_031305 ARHGAP24 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs7660702 3.00E-17 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_031305 ARHGAP24 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs345328 2.91E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_031311 CPVL 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs2252521 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_031311 CPVL 17903298 http://www.ncbi.nlm.nih.gov/pubmed/17903298 "Hemoglobin A, Glycosylated" rs10486607 8.00E-06 Genome-wide association with diabetes-related traits in the Framingham Heart Study. NHGRI|-1
NM_031313 ALPPL2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs790025 3.70E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_031313 ALPPL2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs790025 7.44E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_031314 HNRNPC 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8016099 3.74E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_031314 HNRNPC 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs17197037 2.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_031409 CCR6 20453841 http://www.ncbi.nlm.nih.gov/pubmed/20453841 "Arthritis, Rheumatoid" rs3093024 8.00E-19 A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. NHGRI|-1
NM_031409 CCR6 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs3093023 2.00E-11 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_031415 GSDMC 21037568 http://www.ncbi.nlm.nih.gov/pubmed/21037568 Hodgkin Disease rs2019960 1.00E-13 "A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)." NHGRI|-1
NM_031415 GSDMC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10505508 6.40E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_031415 GSDMC 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs10492294 4.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_031415 GSDMC 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs9792269 3.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_031415 GSDMC 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs975730 2.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_031415 GSDMC 20852632 http://www.ncbi.nlm.nih.gov/pubmed/20852632 Ovarian Neoplasms rs10088218 3.00E-09 A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24. NHGRI|-1
NM_031415 GSDMC 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs6651252 4.00E-18 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_031415 GSDMC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs759944 1.65E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_031415 GSDMC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17818958 1.07E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_031415 GSDMC 19270707 http://www.ncbi.nlm.nih.gov/pubmed/19270707 Cleft Lip rs987525 3.00E-24 Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24. NHGRI|-1
NM_031415 GSDMC 20436469 http://www.ncbi.nlm.nih.gov/pubmed/20436469 Cleft Lip rs987525 4.00E-16 A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4. NHGRI|-1
NM_031415 GSDMC 19656524 http://www.ncbi.nlm.nih.gov/pubmed/19656524 Cleft Lip rs987525 9.00E-08 A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24. NHGRI|-1
NM_031415 GSDMC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs16904056 1.81E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_031415 GSDMC 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs891835 8.00E-11 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_031415 GSDMC 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs10956483 2.00E-10 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_031415 GSDMC 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs4295627 2.00E-18 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_031415 GSDMC 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs4295627 5.00E-21 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_031415 GSDMC 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs6470764 2.00E-28 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_031418 ANO3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs293983 7.79E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_031418 ANO3 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs12295638 4.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_031419 NFKBIZ 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs17842780 1.05E-06 NBL-GWAS version 1 dbGaP|2845
NM_031419 NFKBIZ 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs991258 5.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_031429 RTBDN 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7255045 2.00E-12 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_031438 NUDT12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12516214 1.79E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_031444 C22orf13 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs12170895 5.82E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_031448 C19orf12 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs8102137 2.00E-11 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_031460 KCNK17 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2395721 5.53E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_031460 KCNK17 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs9471058 5.65E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_031460 KCNK17 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10807204 6.70E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_031461 CRISPLD1 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs16939046 4.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_031469 SH3BGRL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1062793 2.80E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_031469 SH3BGRL2 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs346291 3.00E-07 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_031469 SH3BGRL2 21190210 http://www.ncbi.nlm.nih.gov/pubmed/21190210 Obsessive-Compulsive Disorder rs3747767 7.00E-07 Genome-wide association study of hoarding traits. NHGRI|-1
NM_031473 IFT81 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Alpha-Globulins rs11065611 1.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_031476 CRISPLD2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs2326458 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_031480 RIOK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9379104 6.63E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_031844 HNRNPU 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4658673 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_031845 MAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9288410 2.71E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_031845 MAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9288410 3.28E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_031845 MAP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9288410 5.64E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_031892 SH3KBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs16997315 4.66E-11 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_031894 FTHL17 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs5971535 8.37E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_031898 TEKT3 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Forced Expiratory Volume rs2906966 8.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_031900 AGXT2 21572414 http://www.ncbi.nlm.nih.gov/pubmed/21572414 Metabolism rs37369 2.00E-182 A genome-wide association study of metabolic traits in human urine. NHGRI|-1
NM_031907 USP26 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs17324272 2.00E-07 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_031910 C1QTNF6 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs229527 2.00E-16 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_031910 C1QTNF6 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs229541 2.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_031910 C1QTNF6 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs229541 2.00E-08 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_031910 C1QTNF6 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Arthritis, Rheumatoid" rs743777 1.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_031910 C1QTNF6 21653640 http://www.ncbi.nlm.nih.gov/pubmed/21653640 "Arthritis, Rheumatoid" rs743777 2.00E-06 Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways. NHGRI|-1
NM_031910 C1QTNF6 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs229492 7.75E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_031911 C1QTNF7 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs16891867 3.00E-09 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_031911 C1QTNF7 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1861046 6.00E-08 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_031916 ROPN1L 21424380 http://www.ncbi.nlm.nih.gov/pubmed/21424380 Breast Neoplasms rs1092913 2.00E-06 Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility. NHGRI|-1
NM_031917 ANGPTL6 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Thyrotropin rs8109578 4.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_031924 RSPH3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2016588 1.29E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_031924 RSPH3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2057061 3.47E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_031924 RSPH3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9365009 4.19E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_031935 HMCN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10489753 2.90E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_031938 BCO2 20150558 http://www.ncbi.nlm.nih.gov/pubmed/20150558 Interleukin-18 rs2115763 4.00E-09 Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels. NHGRI|-1
NM_031938 BCO2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Interleukin-18 rs2250417 7.00E-13 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_031942 CDCA7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2358259 1.39E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_031942 CDCA7 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Mass Index rs7590983 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_031942 CDCA7 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs7581219 8.57E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_031951 WDR87 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs16975963 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_031954 KCTD10 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs2338104 1.00E-10 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_031954 KCTD10 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, HDL" rs2338104 3.00E-08 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_031954 KCTD10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2058804 6.08E-05 NBL-GWAS version 2 dbGaP|2895
NM_031956 TTC29 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs1395821 7.00E-07 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_032012 C9orf5 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs523340 2.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_032016 STARD3NL 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs1524058 1.00E-09 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_032039 ITFG3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs7189020 2.00E-12 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_032039 ITFG3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1122794 3.00E-10 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_032048 EMILIN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11080995 5.96E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_032116 KATNAL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17505148 7.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_032116 KATNAL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17724817 3.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_032116 KATNAL1 20460270 http://www.ncbi.nlm.nih.gov/pubmed/20460270 Biliary Atresia rs9314986 2.00E-06 Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. NHGRI|-1
NM_032119 GPR98 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Benzodiazepines rs1967256 3.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_032119 GPR98 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10514345 2.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_032122 DTNBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs9296985 1.07E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_032135 FSCB 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs17115674 7.76E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_032137 C3orf20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7651825 2.20E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_032143 ZRANB3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1561277 1.06E-07 NBL-GWAS version 1 dbGaP|2845
NM_032160 DSEL 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs17077540 2.00E-07 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_032160 DSEL 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs2124349 4.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_032166 ATRIP 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs9876781 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_032173 ZNRF3 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs4823006 3.00E-11 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_032199 ARID5B 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs10821936 1.00E-15 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_032199 ARID5B 19684604 http://www.ncbi.nlm.nih.gov/pubmed/19684604 "Leukemia, Lymphoid" rs7089424 7.00E-19 "Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia." NHGRI|-1
NM_032206 NLRC5 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs16965039 6.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_032208 ANTXR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6710260 2.53E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_032226 ZCCHC7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12378217 5.00E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_032228 FAR1 19874204 http://www.ncbi.nlm.nih.gov/pubmed/19874204 Bone Density rs9630182 4.00E-07 IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study. NHGRI|-1
NM_032229 SLITRK6 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs9546711 2.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_032246 MEX3B 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs12324805 7.00E-06 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_032246 MEX3B 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4778944 9.28E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_032251 CCDC88B 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs694739 4.00E-07 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_032251 CCDC88B 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs694739 6.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_032264 NBPF3 19303062 http://www.ncbi.nlm.nih.gov/pubmed/19303062 Vitamin B 6 rs4654748 8.00E-18 "Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations." NHGRI|-1
NM_032264 NBPF3 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs1780324 7.00E-15 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_032264 NBPF3 20558539 http://www.ncbi.nlm.nih.gov/pubmed/20558539 Phosphorus rs1697421 1.00E-27 Common genetic variants associate with serum phosphorus concentration. NHGRI|-1
NM_032266 C2orf16 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs1919128 2.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_032266 C2orf16 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs1260333 2.00E-19 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_032270 LRRC8C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1215582 8.52E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_032276 RHBDD1 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Forced Expiratory Volume rs3820928 5.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_032279 ATP13A4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7630292 1.57E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_032293 GARNL3 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs4130590 3.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_032294 CAMKK1 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs758642 7.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_032295 SLC37A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7777468 6.51E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_032295 SLC37A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6955063 4.02E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_032295 SLC37A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6947516 6.25E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_032313 C4orf14 21106707 http://www.ncbi.nlm.nih.gov/pubmed/21106707 Bleomycin rs708547 9.00E-07 A genetic variant near the PMAIP1/Noxa gene is associated with increased bleomycin sensitivity. NHGRI|-1
NM_032323 TMEM79 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs6684514 3.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_032326 TMEM175 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs6599388 4.00E-12 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_032326 TMEM175 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs6599389 4.00E-08 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_032326 TMEM175 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2290405 1.78E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_032328 EFCAB2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4658673 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_032331 ECE2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs3914188 3.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_032350 C7orf50 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs10256972 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_032352 BRMS1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs8014810 1.54E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_032352 BRMS1L 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs1168987 5.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_032352 BRMS1L 19198613 http://www.ncbi.nlm.nih.gov/pubmed/19198613 Thyroid Neoplasms rs944289 2.00E-09 Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. NHGRI|-1
NM_032377 ELOF1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs7253363 9.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_032408 BAZ1B 21490707 http://www.ncbi.nlm.nih.gov/pubmed/21490707 Caffeine rs2240466 1.00E-06 Genome-wide meta-analysis identifies regions on 7p21 (AHR) and 15q24 (CYP1A2) as determinants of habitual caffeine consumption. NHGRI|-1
NM_032408 BAZ1B 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Triglycerides rs2240466 1.00E-12 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_032408 BAZ1B 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs1178979 2.00E-12 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_032408 BAZ1B 20657596 http://www.ncbi.nlm.nih.gov/pubmed/20657596 Hypertriglyceridemia rs714052 3.00E-06 Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. NHGRI|-1
NM_032408 BAZ1B 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs714052 3.00E-15 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_032408 BAZ1B 20802025 http://www.ncbi.nlm.nih.gov/pubmed/20802025 Protein C rs17145713 3.00E-08 Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. NHGRI|-1
NM_032412 C5orf32 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4913069 9.52E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_032424 KIAA1826 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10895889 7.40E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_032425 HHIPL1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs2895811 1.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_032427 MAML2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10765792 8.00E-13 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_032427 MAML2 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs7115578 8.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_032429 LZTS2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs701837 1.19E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_032430 BRSK1 19448621 http://www.ncbi.nlm.nih.gov/pubmed/19448621 Menarche rs1172822 2.00E-19 Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. NHGRI|-1
NM_032430 BRSK1 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs1172822 6.00E-11 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_032433 ZNF333 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs3885179 6.10E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_032434 ZNF512 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs13022873 5.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_032435 KIAA1804 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs10910200 6.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_032436 ZNF828 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3813131 1.05E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_032436 ZNF828 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3813133 1.67E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_032436 ZNF828 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7316983 1.05E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_032438 L3MBTL3 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs6569648 1.00E-21 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_032438 L3MBTL3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs6899976 6.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_032440 LCOR 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6584099 4.33E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_032447 FBN3 19798445 http://www.ncbi.nlm.nih.gov/pubmed/19798445 Sphingomyelins rs7258249 2.00E-27 Genetic determinants of circulating sphingolipid concentrations in European populations. NHGRI|-1
NM_032454 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs416002 9.33E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_032454 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs389884 8.47E-87 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_032454 STK19 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs389884 2.08E-18 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_032454 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs389884 9.42E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_032454 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs387608 1.91E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_032454 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs387608 6.95E-09 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_032454 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs389883 1.56E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_032454 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs389512 2.34E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_032454 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs389512 9.00E-09 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_032466 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900493 6.94E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_032466 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483170 5.79E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_032466 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483172 6.77E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_032467 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900493 6.94E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_032467 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483170 5.79E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_032467 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483172 6.77E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_032468 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900493 6.94E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_032468 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483170 5.79E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_032468 ASPH 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483172 6.77E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_032470 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2077580 7.45E-32 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_032470 TNXB 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs12198173 3.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_032470 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12198173 8.39E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_032470 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs204878 1.21E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_032470 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs17201560 1.56E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_032470 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs17201560 8.14E-09 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_032470 TNXB 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs185819 3.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_032470 TNXB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130287 2.26E-28 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_032470 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1150754 1.96E-106 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_032470 TNXB 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1150754 6.66E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_032470 TNXB 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs1150754 6.00E-29 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_032470 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1150752 3.64E-86 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_032470 TNXB 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs17421624 1.79E-08 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_032470 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1269854 1.08E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_032470 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1269854 7.53E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_032470 TNXB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3134954 1.40E-108 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_032470 TNXB 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Eosinophils rs2269426 3.00E-06 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_032482 DOT1L 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs12986413 3.00E-08 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_032482 DOT1L 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Mass Index rs3803915 5.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_032485 MCM8 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs236114 1.00E-10 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_032485 MCM8 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs454422 1.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_032485 MCM8 19448621 http://www.ncbi.nlm.nih.gov/pubmed/19448621 Menarche rs16991615 1.00E-21 Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. NHGRI|-1
NM_032491 RFX4 21084426 http://www.ncbi.nlm.nih.gov/pubmed/21084426 Parkinson Disease rs4964469 2.00E-07 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. NHGRI|-1
NM_032491 RFX4 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs3891355 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_032493 AP1M1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12185505 3.68E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_032503 MCHR2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2841307 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_032503 MCHR2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs4840086 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_032503 MCHR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4431442 5.59E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_032505 KBTBD8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4417811 1.52E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_032505 KBTBD8 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Blood Urea Nitrogen rs11709625 2.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_032507 PGBD1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs13211507 6.73E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_032507 PGBD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs13211507 8.18E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_032511 C6orf168 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs2132683 1.00E-06 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_032515 BOK 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs12479254 6.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_032517 LYZL1 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs11007350 3.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_032517 LYZL1 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs1612122 7.00E-06 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_032517 LYZL1 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs533844 2.02E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_032518 COL25A1 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs4956211 1.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_032526 NT5C1A 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs873917 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_032527 ZGPAT 18758464 http://www.ncbi.nlm.nih.gov/pubmed/18758464 Inflammatory Bowel Diseases rs2315008 9.00E-15 Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. NHGRI|-1
NM_032527 ZGPAT 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs4809330 3.00E-15 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_032531 KIRREL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4935969 1.89E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_032531 KIRREL3 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs4935969 4.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_032531 KIRREL3 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs1557488 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_032531 KIRREL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs1557488 7.69E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_032531 KIRREL3 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Insulin-Like Growth Factor I rs1939992 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_032531 KIRREL3 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs620875 3.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_032532 FNDC1 21606135 http://www.ncbi.nlm.nih.gov/pubmed/21606135 Coronary Artery Disease rs365302 8.00E-07 A Genome-wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease. NHGRI|-1
NM_032532 FNDC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs10806706 6.83E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_032532 FNDC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs4708818 6.79E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_032532 FNDC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs12197995 1.53E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_032532 FNDC1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs212388 2.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_032532 FNDC1 21298027 http://www.ncbi.nlm.nih.gov/pubmed/21298027 Intestinal Diseases rs212388 2.00E-10 "A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease." NHGRI|-1
NM_032536 NTNG2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs11243676 3.00E-06 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_032549 IMMP2L 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs10279573 3.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_032549 IMMP2L 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs12531640 6.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_032549 IMMP2L 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs6968385 2.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_032552 DAB2IP 20622881 http://www.ncbi.nlm.nih.gov/pubmed/20622881 "Aortic Aneurysm, Abdominal" rs7025486 5.00E-10 Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm. NHGRI|-1
NM_032556 IL1F10 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Interleukin 1 Receptor Antagonist Protein rs6761276 7.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_032556 IL1F10 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs6734238 2.00E-17 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_032558 HIATL1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs16910061 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_032563 LCE3D 19169255 http://www.ncbi.nlm.nih.gov/pubmed/19169255 Psoriasis rs4085613 7.00E-30 Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21. NHGRI|-1
NM_032563 LCE3D 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs4112788 3.00E-10 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_032573 CCDC62 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs12817488 3.00E-13 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_032578 MYPN 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Optic Nerve rs6480314 2.00E-07 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_032581 FAM126A 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2270101 3.88E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_032600 CCDC54 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7610766 7.23E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_032600 CCDC54 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1850344 4.72E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_032600 CCDC54 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10511260 3.41E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_032600 CCDC54 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs9863794 3.29E-05 NBL-GWAS version 2 dbGaP|2895
NM_032608 MYO18B 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs8139900 4.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_032608 MYO18B 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Mental Disorders rs1001021 2.00E-06 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_032608 MYO18B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2049988 1.28E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_032611 PTP4A3 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs7839244 6.76E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_032622 LNX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1391759 1.78E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_032622 LNX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1391759 6.11E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_032622 LNX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1391758 1.84E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_032622 LNX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1391758 6.29E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_032626 RBBP6 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs11643520 6.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_032632 PAPOLA 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs17094273 9.00E-08 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_032636 PSRC1 20442857 http://www.ncbi.nlm.nih.gov/pubmed/20442857 1-Alkyl-2-acetylglycerophosphocholine Esterase rs599839 3.00E-15 Genome-wide association study of Lp-PLA(2) activity and mass in the Framingham Heart Study. NHGRI|-1
NM_032636 PSRC1 18262040 http://www.ncbi.nlm.nih.gov/pubmed/18262040 "Cholesterol, LDL" rs599839 1.00E-33 LDL-cholesterol concentrations: a genome-wide association study. NHGRI|-1
NM_032636 PSRC1 18179892 http://www.ncbi.nlm.nih.gov/pubmed/18179892 "Cholesterol, LDL" rs599839 1.00E-07 Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. NHGRI|-1
NM_032636 PSRC1 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs599839 6.00E-33 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_032636 PSRC1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs599839 3.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_032636 PSRC1 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs599839 4.00E-09 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_032643 IRF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs7808907 6.08E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_032643 IRF5 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs10488631 4.00E-11 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_032643 IRF5 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs10488631 2.00E-07 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_032643 IRF5 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs10488631 3.00E-10 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_032643 IRF5 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 1.65E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_032643 IRF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10488631 2.48E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_032643 IRF5 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 2.00E-11 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_032643 IRF5 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs10488631 7.00E-18 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_032643 IRF5 20383147 http://www.ncbi.nlm.nih.gov/pubmed/20383147 "Scleroderma, Systemic" rs10488631 2.00E-13 Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. NHGRI|-1
NM_032643 IRF5 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs10488631 4.00E-07 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_032643 IRF5 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs4728142 2.00E-08 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_032643 IRF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs4728142 7.30E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_032643 IRF5 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs4728142 8.00E-19 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_032646 TTYH2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs7219585 1.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_032647 CBX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs3751954 9.51E-06 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_032649 CNDP1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7245160 4.22E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_032679 ZNF577 21424380 http://www.ncbi.nlm.nih.gov/pubmed/21424380 Breast Neoplasms rs10411161 7.00E-06 Potential novel candidate polymorphisms identified in genome-wide association study for breast cancer susceptibility. NHGRI|-1
NM_032680 EFCAB4B 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs887304 8.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_032680 EFCAB4B 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs242033 3.73E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_032680 EFCAB4B 19478329 http://www.ncbi.nlm.nih.gov/pubmed/19478329 "Infertility, Male" rs10848911 4.00E-06 Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. NHGRI|-1
NM_032682 FOXP1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs17651978 6.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_032682 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9819066 4.55E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_032682 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9828629 8.89E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_032682 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6549392 2.33E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_032682 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11720523 2.09E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_032682 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6779258 1.11E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_032682 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11720121 1.28E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_032682 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6549400 8.46E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_032682 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10460943 7.33E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_032682 FOXP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs1090502 8.12E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_032682 FOXP1 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Mass Index rs1024889 6.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_032693 NAA11 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1455311 1.00E-18 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_032718 MFSD9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs955916 1.30E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_032725 BUD13 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs28927680 2.00E-17 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_032725 BUD13 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs11825181 3.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_032725 BUD13 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs11820589 6.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_032725 BUD13 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs10790162 3.00E-15 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_032725 BUD13 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs10790162 5.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_032725 BUD13 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs10790162 7.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_032725 BUD13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1009746 1.83E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_032725 BUD13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1009746 4.03E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_032725 BUD13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17473320 8.79E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_032725 BUD13 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs490592 1.00E-06 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_032725 BUD13 21160409 http://www.ncbi.nlm.nih.gov/pubmed/21160409 HIV-1 rs1240773 8.00E-06 Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population. NHGRI|-1
NM_032725 BUD13 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs4938303 4.00E-21 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_032725 BUD13 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Triglycerides rs7350481 1.00E-49 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_032725 BUD13 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs180358 6.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_032725 BUD13 19185284 http://www.ncbi.nlm.nih.gov/pubmed/19185284 alpha-Tocopherol rs12272004 8.00E-10 "Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study." NHGRI|-1
NM_032725 BUD13 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs12272004 7.00E-07 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_032725 BUD13 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Triglycerides rs12272004 5.00E-13 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_032725 BUD13 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs1558861 2.00E-06 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_032725 BUD13 18193046 http://www.ncbi.nlm.nih.gov/pubmed/18193046 Triglycerides rs1558861 2.00E-26 Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. NHGRI|-1
NM_032725 BUD13 20838585 http://www.ncbi.nlm.nih.gov/pubmed/20838585 Triglycerides rs12280753 8.00E-06 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. NHGRI|-1
NM_032738 FCRLA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1538972 7.81E-05 NBL-GWAS version 2 dbGaP|2895
NM_032741 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11553430 2.45E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_032741 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130284 1.39E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_032741 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130284 4.39E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_032741 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3134945 1.24E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_032741 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3134945 4.06E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_032741 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3132965 8.39E-16 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_032741 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130349 5.68E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_032741 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130349 9.28E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_032741 AGPAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3134943 2.82E-105 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_032744 C6orf105 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs6457906 5.45E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_032752 ZNF496 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10399826 2.06E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_032752 ZNF496 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11802371 1.11E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_032776 JMJD1C 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs12355784 5.00E-10 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_032776 JMJD1C 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs2393967 3.00E-21 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_032776 JMJD1C 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs2893923 5.00E-08 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_032776 JMJD1C 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs10761779 7.00E-10 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_032777 GPR124 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs6468442 3.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_032784 RSPO3 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs9491696 1.00E-11 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_032784 RSPO3 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs9491696 2.00E-32 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_032784 RSPO3 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs13204965 3.00E-08 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_032784 RSPO3 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs972275 2.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_032785 AGBL4 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs17105335 5.42E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_032795 RPUSD4 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs563519 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_032806 C3orf39 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs17075286 8.00E-07 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_032808 LINGO1 19182806 http://www.ncbi.nlm.nih.gov/pubmed/19182806 Essential Tremor rs9652490 1.00E-09 Variant in the sequence of the LINGO1 gene confers risk of essential tremor. NHGRI|-1
NM_032812 PLXDC2 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs1571942 3.00E-07 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_032812 PLXDC2 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs12219125 9.00E-09 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_032812 PLXDC2 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs12772794 7.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_032812 PLXDC2 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs16920624 7.00E-07 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_032812 PLXDC2 20610895 http://www.ncbi.nlm.nih.gov/pubmed/20610895 Vascular Diseases rs2359536 2.00E-06 Identification of evidence suggestive of an association with peripheral arterial disease at the OSBPL10 locus by genome-wide investigation in the Japanese population. NHGRI|-1
NM_032816 CCDC123 20383145 http://www.ncbi.nlm.nih.gov/pubmed/20383145 Kidney Diseases rs4805834 5.00E-11 Genetic loci influencing kidney function and chronic kidney disease. NHGRI|-1
NM_032816 CCDC123 21572414 http://www.ncbi.nlm.nih.gov/pubmed/21572414 Metabolism rs8101881 6.00E-27 A genome-wide association study of metabolic traits in human urine. NHGRI|-1
NM_032817 ITIH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs4748940 3.09E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_032819 ZNF341 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs7274811 1.00E-20 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_032819 ZNF341 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs7274811 6.00E-22 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_032823 C9orf3 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs3802458 4.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_032834 ALG10 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs9300212 8.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_032852 ATG4C 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs17124318 6.00E-07 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_032852 ATG4C 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs17124318 4.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_032852 ATG4C 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs10493340 2.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_032852 ATG4C 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs12130333 2.00E-08 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_032866 CGNL1 21305692 http://www.ncbi.nlm.nih.gov/pubmed/21305692 Bipolar Disorder rs2934442 1.00E-06 Genome-wide association analysis of age at onset and psychotic symptoms in bipolar disorder. NHGRI|-1
NM_032867 MICALCL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10831798 2.78E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_032867 MICALCL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4757381 8.95E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_032875 FBXL20 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs7208487 8.00E-07 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_032880 IGSF21 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs3007729 5.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_032880 IGSF21 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs16861326 2.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_032883 TOX2 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs6031252 6.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_032883 TOX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6073330 3.85E-05 NBL-GWAS version 2 dbGaP|2895
NM_032883 TOX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11696193 6.20E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_032884 C1orf94 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2994598 3.11E-06 NBL-GWAS version 1 dbGaP|2845
NM_032884 C1orf94 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs10914952 1.64E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_032884 C1orf94 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2359631 6.37E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_032884 C1orf94 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs612353 9.05E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_032888 COL27A1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs946053 2.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_032905 RBM17 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs12251307 1.00E-13 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_032905 RBM17 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs12251307 2.00E-06 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_032927 TMEM128 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2920228 2.92E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_032927 TMEM128 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2920228 3.32E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_032932 RAB11FIP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs315437 1.71E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_032936 TMEM60 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Creatinine rs6465825 2.00E-09 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_032945 RTEL1 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs6010620 2.00E-09 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_032945 RTEL1 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs6010620 3.00E-12 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_032945 RTEL1 19578366 http://www.ncbi.nlm.nih.gov/pubmed/19578366 Glioma rs6010620 3.00E-09 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. NHGRI|-1
NM_032945 RTEL1 19578366 http://www.ncbi.nlm.nih.gov/pubmed/19578366 Glioma rs4809324 2.00E-09 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. NHGRI|-1
NM_032945 RTEL1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2297441 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_032951 MLXIPL 18193046 http://www.ncbi.nlm.nih.gov/pubmed/18193046 Triglycerides rs3812316 1.00E-10 Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. NHGRI|-1
NM_032952 MLXIPL 18193046 http://www.ncbi.nlm.nih.gov/pubmed/18193046 Triglycerides rs3812316 1.00E-10 Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. NHGRI|-1
NM_032953 MLXIPL 18193046 http://www.ncbi.nlm.nih.gov/pubmed/18193046 Triglycerides rs3812316 1.00E-10 Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. NHGRI|-1
NM_032954 MLXIPL 18193046 http://www.ncbi.nlm.nih.gov/pubmed/18193046 Triglycerides rs3812316 1.00E-10 Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. NHGRI|-1
NM_032955 AIF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2269475 4.48E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_032955 AIF1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2736177 3.15E-23 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_032957 RTEL1 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs6010620 2.00E-09 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_032957 RTEL1 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs6010620 3.00E-12 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_032957 RTEL1 19578366 http://www.ncbi.nlm.nih.gov/pubmed/19578366 Glioma rs6010620 3.00E-09 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. NHGRI|-1
NM_032957 RTEL1 19578366 http://www.ncbi.nlm.nih.gov/pubmed/19578366 Glioma rs4809324 2.00E-09 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. NHGRI|-1
NM_032957 RTEL1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2297441 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_032966 CXCR5 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs6421571 3.00E-12 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_032967 PCDH11X 19136949 http://www.ncbi.nlm.nih.gov/pubmed/19136949 Alzheimer Disease rs2573905 2.00E-07 Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease. NHGRI|-1
NM_032968 PCDH11X 19136949 http://www.ncbi.nlm.nih.gov/pubmed/19136949 Alzheimer Disease rs2573905 2.00E-07 Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease. NHGRI|-1
NM_032969 PCDH11X 19136949 http://www.ncbi.nlm.nih.gov/pubmed/19136949 Alzheimer Disease rs2573905 2.00E-07 Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's disease. NHGRI|-1
NM_032997 ZWINT 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs4462262 9.00E-08 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_032997 ZWINT 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs35866326 4.02E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_032997 ZWINT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11005196 3.65E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_032997 ZWINT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs11005240 4.15E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_033012 TNFSF11 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1325803 1.57E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_033012 TNFSF11 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs9533090 5.00E-25 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_033012 TNFSF11 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs9594738 2.00E-08 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_033012 TNFSF11 21533022 http://www.ncbi.nlm.nih.gov/pubmed/21533022 Bone Density rs9594738 4.00E-06 Genome-wide association study using extreme truncate selection identifies novel genes affecting bone mineral density and fracture risk. NHGRI|-1
NM_033012 TNFSF11 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs9594759 2.00E-17 New sequence variants associated with bone mineral density. NHGRI|-1
NM_033012 TNFSF11 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs9594759 2.00E-21 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_033012 TNFSF11 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs2062305 5.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_033012 TNFSF11 21124946 http://www.ncbi.nlm.nih.gov/pubmed/21124946 Bone Density rs1021188 2.00E-14 Genome-wide association meta-analysis of cortical bone mineral density unravels allelic heterogeneity at the RANKL locus and potential pleiotropic effects on bone. NHGRI|-1
NM_033016 PDGFB 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs2413583 1.00E-26 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_033016 PDGFB 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs968451 1.00E-09 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_033016 PDGFB 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs54211 8.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_033017 TRIM4 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs17277546 2.00E-11 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_033022 RPS24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1916400 1.80E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_033022 RPS24 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs2395528 6.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_033022 RPS24 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs35648 3.27E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_033026 PCLO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2715148 1.46E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_033026 PCLO 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs2715148 1.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_033026 PCLO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2522833 1.54E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_033026 PCLO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2522840 2.85E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_033026 PCLO 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2107828 5.11E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_033026 PCLO 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Mortality rs2371208 3.00E-06 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_033030 BOLL 18997786 http://www.ncbi.nlm.nih.gov/pubmed/18997786 Intracranial Aneurysm rs700651 4.00E-08 Susceptibility loci for intracranial aneurysm in European and Japanese populations. NHGRI|-1
NM_033035 TSLP 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs3806932 3.00E-09 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_033050 SUCNR1 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs6798928 3.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_033055 HIAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs560659 1.01E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_033056 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs11004359 5.25E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_033056 PCDH15 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs10740609 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_033056 PCDH15 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs1916521 5.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_033056 PCDH15 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12412945 5.50E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_033056 PCDH15 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 C-Reactive Protein rs583012 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_033056 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1932011 8.49E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_033056 PCDH15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9416295 9.93E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_033071 SYNE1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs2673776 8.05E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_033071 SYNE1 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs17082664 1.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_033071 SYNE1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs17082664 4.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_033071 SYNE1 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs7747960 9.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_033071 SYNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2623963 7.61E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_033071 SYNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7745725 1.87E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_033071 SYNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1358317 1.61E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_033071 SYNE1 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs1322512 8.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_033089 ZCCHC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6082956 6.19E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_033091 TRIM4 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs17277546 2.00E-11 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_033102 SLC45A3 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs12748961 4.00E-08 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_033103 RHPN2 19011631 http://www.ncbi.nlm.nih.gov/pubmed/19011631 Colorectal Neoplasms rs10411210 5.00E-09 Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. NHGRI|-1
NM_033109 PNPT1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs7577894 1.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_033119 NKD1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs8054797 1.11E-08 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_033119 NKD1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs8044151 6.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_033125 SLC22A16 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9481083 9.76E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_033127 SEC16B 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs10913469 6.00E-08 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_033127 SEC16B 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs10913469 1.00E-08 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_033127 SEC16B 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs633715 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_033127 SEC16B 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs543874 4.00E-23 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_033132 ZIC5 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs7992643 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_033135 PDGFD 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs10895547 3.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_033135 PDGFD 21118971 http://www.ncbi.nlm.nih.gov/pubmed/21118971 Small Cell Lung Carcinoma rs716274 9.00E-08 Genome-wide interrogation identifies YAP1 variants associated with survival of small-cell lung cancer patients. NHGRI|-1
NM_033135 PDGFD 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs1917445 6.00E-07 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_033135 PDGFD 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs974819 2.00E-09 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_033136 FGF1 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs152528 8.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_033137 FGF1 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs152528 8.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_033138 CALD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12539126 8.96E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_033138 CALD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10488456 6.08E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_033139 CALD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12539126 8.96E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_033139 CALD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10488456 6.08E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_033140 CALD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12539126 8.96E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_033140 CALD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10488456 6.08E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_033141 MAP3K9 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs17108533 1.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_033141 MAP3K9 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs36563 5.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_033143 FGF5 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs16998073 1.00E-21 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_033147 DTNB 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11684202 6.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_033148 DTNB 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11684202 6.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_033150 COL2A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1793949 3.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_033157 CALD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12539126 8.96E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_033157 CALD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10488456 6.08E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_033158 HYAL2 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs11130248 5.00E-07 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_033159 HYAL1 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs11130248 5.00E-07 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_033177 BAT4 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3130618 9.99E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_033181 CNR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs964647 2.09E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_033204 ZNF101 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs2304130 2.00E-15 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_033204 ZNF101 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Triglycerides rs2304130 3.00E-06 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_033204 ZNF101 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs2304130 4.00E-08 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_033204 ZNF101 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs2304130 9.71E-06 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_033211 C5orf30 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs26232 4.00E-08 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_033211 C5orf30 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12516214 1.79E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_033223 GABRG3 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7180500 6.79E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_033223 GABRG3 19772629 http://www.ncbi.nlm.nih.gov/pubmed/19772629 Parkinson Disease rs17565841 3.00E-06 Genomewide association study for onset age in Parkinson disease. NHGRI|-1
NM_033225 CSMD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7013027 1.85E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_033225 CSMD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs6992732 3.32E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_033225 CSMD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7844468 2.74E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_033225 CSMD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7813351 7.28E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_033225 CSMD1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1529316 1.20E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_033225 CSMD1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1529316 2.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_033225 CSMD1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2049306 1.60E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_033225 CSMD1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs4875320 6.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_033225 CSMD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6986423 1.27E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_033225 CSMD1 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs641525 5.00E-07 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_033229 TRIM15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2107195 1.68E-17 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_033229 TRIM15 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs929156 1.30E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_033229 TRIM15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs112960140 6.18E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_033229 TRIM15 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs2844786 1.70E-07 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_033238 PML 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs5742915 5.00E-07 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_033238 PML 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs5742915 2.00E-14 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_033239 PML 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs5742915 5.00E-07 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_033239 PML 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs5742915 2.00E-14 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_033240 PML 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs5742915 5.00E-07 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_033240 PML 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs5742915 2.00E-14 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_033244 PML 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs5742915 5.00E-07 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_033244 PML 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs5742915 2.00E-14 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_033246 PML 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs5742915 5.00E-07 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_033246 PML 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs5742915 2.00E-14 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_033247 PML 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs5742915 5.00E-07 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_033247 PML 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs5742915 2.00E-14 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_033250 PML 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs5742915 5.00E-07 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_033250 PML 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs5742915 2.00E-14 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_033253 NT5C1B 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognition rs1876040 6.00E-08 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_033256 PPP1R14A 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs8102476 2.00E-11 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_033260 FOXQ1 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs9502893 3.00E-07 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_033260 FOXQ1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1883628 5.86E-05 NBL-GWAS version 2 dbGaP|2895
NM_033262 SLC8A3 21602797 http://www.ncbi.nlm.nih.gov/pubmed/21602797 Cystic Fibrosis rs12883884 8.00E-06 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. NHGRI|-1
NM_033267 IRX2 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs12653946 4.00E-18 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_033267 IRX2 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs6879627 8.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_033267 IRX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs370672 6.66E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_033272 KCNH7 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs17716942 1.00E-13 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_033272 KCNH7 19680635 http://www.ncbi.nlm.nih.gov/pubmed/19680635 "Parkinson Disease, Secondary" rs12476047 3.00E-06 Genome-wide association study of antipsychotic-induced parkinsonism severity among schizophrenia patients. NHGRI|-1
NM_033274 ADAM19 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs2277027 1.00E-10 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_033274 ADAM19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11740562 1.61E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_033274 ADAM19 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11740562 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_033280 SEC11C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9961404 1.02E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_033280 SEC11C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1517037 6.81E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_033280 SEC11C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9319943 3.34E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_033285 TP53INP1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs896854 1.00E-09 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_033289 MID1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs5934953 1.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_033289 MID1 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs12388359 4.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_033290 MID1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs5934953 1.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_033290 MID1 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs12388359 4.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_033300 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs5177 5.00E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_033300 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11206127 3.16E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_033300 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs869987 4.54E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_033300 LRP8 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs114216682 7.00E-08 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_033300 LRP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17785382 1.74E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_033305 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11145323 7.08E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_033305 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2150901 5.11E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_033305 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2183863 4.74E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_033305 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7030802 7.12E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_033305 VPS13A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1574144 3.30E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_033326 SOX6 19714249 http://www.ncbi.nlm.nih.gov/pubmed/19714249 Obesity rs297325 4.00E-07 Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males. NHGRI|-1
NM_033326 SOX6 19714249 http://www.ncbi.nlm.nih.gov/pubmed/19714249 Obesity rs4756846 5.00E-07 Powerful bivariate genome-wide association analyses suggest the SOX6 gene influencing both obesity and osteoporosis phenotypes in males. NHGRI|-1
NM_033326 SOX6 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs7117858 6.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_033326 SOX6 21104366 http://www.ncbi.nlm.nih.gov/pubmed/21104366 Bone Density rs11023787 5.00E-16 A genome-wide association analysis implicates SOX6 as a candidate gene for wrist bone mass. NHGRI|-1
NM_033342 TRIM7 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs1279750 2.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_033360 KRAS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10505975 1.43E-05 NBL-GWAS version 2 dbGaP|2895
NM_033379 CDK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4132554 7.66E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_033390 ZC3H12C 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 Exercise Test rs746463 5.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_033393 FHDC1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs11099864 9.00E-06 Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_033394 TANC1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs13022357 1.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_033400 ZFHX2 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs223116 3.00E-08 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_033401 CNTNAP4 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs13330107 9.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_033406 FBXO3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4756052 3.29E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_033407 DOCK7 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Triglycerides rs1167998 2.00E-12 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_033407 DOCK7 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs1168013 6.00E-08 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_033407 DOCK7 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs1748195 2.00E-10 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_033407 DOCK7 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs10889353 8.00E-06 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_033407 DOCK7 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs10889353 4.00E-12 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_033407 DOCK7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs10889353 4.07E-05 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_033407 DOCK7 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs10889353 3.00E-07 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_033414 ZNF622 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs26017 3.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033414 ZNF622 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs163065 1.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033414 ZNF622 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs171817 3.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033426 KIAA1737 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs17105232 1.50E-05 NBL-GWAS version 2 dbGaP|2895
NM_033427 CTTNBP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12706164 5.23E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_033427 CTTNBP2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7456706 8.33E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_033428 C9orf123 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Braces rs1535480 4.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_033428 C9orf123 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7044355 1.00E-07 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_033428 C9orf123 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10815798 6.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_033428 C9orf123 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12349302 5.86E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_033428 C9orf123 21160409 http://www.ncbi.nlm.nih.gov/pubmed/21160409 HIV-1 rs842304 4.00E-06 Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population. NHGRI|-1
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12510138 7.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1383532 6.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6534139 4.40E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6835635 3.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs13128602 3.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1552095 3.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1010740 3.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs3736115 2.10E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17050695 5.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs1845344 7.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11098524 7.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9993199 9.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2389803 1.12E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1480931 1.11E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10518329 1.12E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10006706 6.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6849561 7.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033430 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12508504 9.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12510138 7.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1383532 6.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6534139 4.40E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6835635 3.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs13128602 3.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1552095 3.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1010740 3.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs3736115 2.10E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17050695 5.00E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs1845344 7.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11098524 7.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9993199 9.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2389803 1.12E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1480931 1.11E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10518329 1.12E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10006706 6.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6849561 7.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033437 PDE5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12508504 9.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_033439 IL33 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs1342326 9.00E-10 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_033440 CELA2A 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs2901964 5.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_033446 FAM125B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs888219 2.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_033452 TRIM47 21681796 http://www.ncbi.nlm.nih.gov/pubmed/21681796 Cerebrum rs1055129 3.00E-11 Genome-wide association studies of cerebral white matter lesion burden: The CHARGE consortium. NHGRI|-1
NM_033453 ITPA 20637204 http://www.ncbi.nlm.nih.gov/pubmed/20637204 Anemia rs1127354 4.00E-44 ITPA polymorphism affects ribavirin-induced anemia and outcomes of therapy--a genome-wide study of Japanese HCV virus patients. NHGRI|-1
NM_033453 ITPA 21659334 http://www.ncbi.nlm.nih.gov/pubmed/21659334 "Hepatitis C, Chronic" rs6139030 1.00E-15 Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C. NHGRI|-1
NM_033453 ITPA 21659334 http://www.ncbi.nlm.nih.gov/pubmed/21659334 "Hepatitis C, Chronic" rs6139030 2.00E-25 Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C. NHGRI|-1
NM_033467 MMEL1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs3748816 3.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_033467 MMEL1 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 "Arthritis, Rheumatoid" rs3890745 1.00E-07 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_033467 MMEL1 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs3890745 4.00E-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_033495 KLHL13 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs2430212 2.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_033496 HK1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs16926246 2.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_033496 HK1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs16926246 1.00E-13 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_033496 HK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs16926246 3.00E-54 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_033496 HK1 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs7072268 2.00E-25 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_033497 HK1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs16926246 2.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_033497 HK1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs16926246 1.00E-13 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_033497 HK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs16926246 3.00E-54 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_033497 HK1 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs7072268 2.00E-25 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_033498 HK1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs16926246 2.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_033498 HK1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs16926246 1.00E-13 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_033498 HK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs16926246 3.00E-54 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_033498 HK1 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs7072268 2.00E-25 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_033500 HK1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs16926246 2.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_033500 HK1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs16926246 1.00E-13 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_033500 HK1 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs16926246 3.00E-54 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_033500 HK1 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs7072268 2.00E-25 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_033503 BMF 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs7181230 5.00E-11 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_033507 GCK 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs730497 6.00E-12 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_033507 GCK 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1799884 1.00E-20 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_033507 GCK 19060907 http://www.ncbi.nlm.nih.gov/pubmed/19060907 Blood Glucose rs4607517 1.00E-25 Variants in MTNR1B influence fasting glucose levels. NHGRI|-1
NM_033507 GCK 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4607517 7.00E-92 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_033507 GCK 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs4607517 2.00E-16 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_033508 GCK 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs730497 6.00E-12 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_033508 GCK 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1799884 1.00E-20 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_033508 GCK 19060907 http://www.ncbi.nlm.nih.gov/pubmed/19060907 Blood Glucose rs4607517 1.00E-25 Variants in MTNR1B influence fasting glucose levels. NHGRI|-1
NM_033508 GCK 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs4607517 7.00E-92 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_033508 GCK 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs4607517 2.00E-16 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_033512 TSPYL5 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs6468544 8.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NM_033512 TSPYL5 20802479 http://www.ncbi.nlm.nih.gov/pubmed/20802479 Migraine Disorders rs1835740 2.00E-11 Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. NHGRI|-1
NM_033515 ARHGAP18 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4310078 1.47E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_033515 ARHGAP18 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Mass Index rs2275215 4.00E-07 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_033542 SYS1 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs1008953 1.00E-07 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_033543 CEACAM21 21682944 http://www.ncbi.nlm.nih.gov/pubmed/21682944 Schizophrenia rs4803480 1.00E-07 DOCK4 and CEACAM21 as novel schizophrenia candidate genes in the Jewish population. NHGRI|-1
NM_033547 INTS4 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4944178 3.27E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_033632 FBXW7 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs360929 9.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_033646 CDH7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17074003 4.56E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_033646 CDH7 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs8083346 6.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_033646 CDH7 21041692 http://www.ncbi.nlm.nih.gov/pubmed/21041692 Heart Function Tests rs470490 5.00E-06 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. NHGRI|-1
NM_033668 ITGB1 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs11009175 5.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_044472 CDC42 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2473323 3.13E-09 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_048368 CTDP1 20801717 http://www.ncbi.nlm.nih.gov/pubmed/20801717 Amyotrophic Lateral Sclerosis rs4799088 9.00E-06 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. NHGRI|-1
NM_048368 CTDP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs537962 1.39E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_048368 CTDP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4799092 2.00E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_052813 CARD9 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs10781499 3.00E-19 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_052813 CARD9 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs4077515 5.00E-08 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_052813 CARD9 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs4077515 1.00E-36 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_052813 CARD9 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs10781500 7.00E-06 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_052813 CARD9 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs10781500 1.00E-06 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_052814 CARD9 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs10781499 3.00E-19 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_052814 CARD9 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs4077515 5.00E-08 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_052814 CARD9 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs4077515 1.00E-36 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_052814 CARD9 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs10781500 7.00E-06 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_052814 CARD9 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs10781500 1.00E-06 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_052828 TRIM10 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs9468692 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_052828 TRIM10 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs9261535 1.70E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_052834 WDR7 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1557351 4.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_052837 SCAMP3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs1142287 2.00E-13 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_052843 OBSCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs435776 5.30E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_052845 MMAB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7134594 6.48E-05 NBL-GWAS version 2 dbGaP|2895
NM_052845 MMAB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs3759387 9.45E-05 NBL-GWAS version 2 dbGaP|2895
NM_052845 MMAB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7486178 3.90E-06 NBL-GWAS version 2 dbGaP|2895
NM_052851 STARD13 20364137 http://www.ncbi.nlm.nih.gov/pubmed/20364137 Intracranial Aneurysm rs9315204 3.00E-09 Genome-wide association study of intracranial aneurysm identifies three new risk loci. NHGRI|-1
NM_052854 CREB3L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11038830 1.81E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_052859 RFT1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2336725 1.00E-12 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_052860 ZNF300 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs1000113 3.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_052860 ZNF300 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs11747270 3.00E-16 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_052860 ZNF300 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs7714584 8.00E-19 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_052866 ADAMTSL1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10963676 1.76E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_052866 ADAMTSL1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10963676 4.79E-07 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_052866 ADAMTSL1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs10810865 4.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_052866 ADAMTSL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs1755289 9.84E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_052866 ADAMTSL1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1755289 3.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_052866 ADAMTSL1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1755289 9.10E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_052866 ADAMTSL1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs2210327 7.00E-07 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_052867 NALCN 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2044117 5.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_052867 NALCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2044117 1.34E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_052867 NALCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9518366 9.14E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_052867 NALCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs3751403 2.10E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_052867 NALCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs12430088 5.11E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_052869 TTYH2 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs7219585 1.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_052870 SNX18 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4865879 6.81E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_052870 SNX18 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10940434 3.27E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_052873 C14orf179 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs935334 3.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_052885 SLC2A13 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson Disease rs1994090 3.00E-08 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_052885 SLC2A13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10784359 2.01E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_052885 SLC2A13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2896905 5.03E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_052892 PKD1L2 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs4889240 7.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_052892 PKD1L2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs9931907 1.18E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_052892 PKD1L2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs8060294 9.40E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_052892 PKD1L2 19185284 http://www.ncbi.nlm.nih.gov/pubmed/19185284 beta Carotene rs6564851 2.00E-24 "Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study." NHGRI|-1
NM_052893 BTBD9 17637780 http://www.ncbi.nlm.nih.gov/pubmed/17637780 Restless Legs Syndrome rs9296249 4.00E-18 Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. NHGRI|-1
NM_052893 BTBD9 17634447 http://www.ncbi.nlm.nih.gov/pubmed/17634447 Restless Legs Syndrome rs3923809 1.00E-17 A genetic risk factor for periodic limb movements in sleep. NHGRI|-1
NM_052896 CSMD2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs416391 3.99E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_052896 CSMD2 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs476463 1.00E-06 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_052896 CSMD2 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2281597 5.00E-07 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_052896 CSMD2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2358756 2.73E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_052896 CSMD2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2164581 6.82E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_052896 CSMD2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs10914850 6.97E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_052898 XKR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2939678 7.11E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_052898 XKR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1532899 1.24E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_052898 XKR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4738287 1.12E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_052898 XKR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6988277 3.20E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_052898 XKR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10107657 3.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_052898 XKR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4738382 2.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_052907 TMEM132B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7134868 1.12E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_052907 TMEM132B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2108521 9.96E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_052907 TMEM132B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10847023 8.38E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_052910 SLITRK1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9545903 7.18E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_052917 GALNT13 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Menopause rs958672 2.00E-06 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_052917 GALNT13 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs707040 6.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_052918 SORCS1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2245437 6.05E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_052918 SORCS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1931605 1.68E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_052918 SORCS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11592212 5.16E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_052920 KLHL29 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs4665630 1.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_052920 KLHL29 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs515135 2.00E-20 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_052920 KLHL29 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs515135 5.00E-29 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_052920 KLHL29 18262040 http://www.ncbi.nlm.nih.gov/pubmed/18262040 "Cholesterol, LDL" rs562338 1.00E-09 LDL-cholesterol concentrations: a genome-wide association study. NHGRI|-1
NM_052920 KLHL29 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs562338 6.00E-22 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_052920 KLHL29 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, LDL" rs541041 8.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_052920 KLHL29 20657596 http://www.ncbi.nlm.nih.gov/pubmed/20657596 Hypertriglyceridemia rs4635554 2.00E-07 Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. NHGRI|-1
NM_052920 KLHL29 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs219553 7.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_052920 KLHL29 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs1117324 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_052920 KLHL29 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10495717 1.31E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_052920 KLHL29 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1562900 9.25E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_052920 KLHL29 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs949978 4.94E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_052920 KLHL29 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs6733000 2.01E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_052920 KLHL29 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1605834 5.11E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_052920 KLHL29 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs13015955 4.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_052920 KLHL29 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs2681019 8.00E-08 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_052920 KLHL29 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs1449984 7.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_052920 KLHL29 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs2577720 8.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_052931 SLAMF6 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs16832015 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_052934 SLC26A9 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Antipsychotic Agents rs11240594 1.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_052937 PCMTD1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10104090 4.42E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_052947 ALPK2 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs8099014 6.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_052954 CYYR1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2830495 7.65E-06 NBL-GWAS version 1 dbGaP|2845
NM_052954 CYYR1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs229040 5.15E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_052956 ACSM1 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs151222 6.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_052956 ACSM1 20185149 http://www.ncbi.nlm.nih.gov/pubmed/20185149 Schizophrenia rs433598 3.00E-06 Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort. NHGRI|-1
NM_052962 IL22RA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4896243 2.67E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_052964 CLNK 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10516213 7.26E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_052965 TSEN15 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs2274432 8.00E-09 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_052968 APOA5 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs2266788 5.00E-13 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_052968 APOA5 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2266788 2.00E-16 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_052968 APOA5 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2266788 2.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_052968 APOA5 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2266788 4.00E-08 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_052968 APOA5 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs1263173 2.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_052968 APOA5 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Triglycerides rs7396835 1.00E-09 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_052987 CDK10 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs258322 2.00E-23 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_052987 CDK10 19578364 http://www.ncbi.nlm.nih.gov/pubmed/19578364 Melanoma rs258322 3.00E-27 Genome-wide association study identifies three loci associated with melanoma risk. NHGRI|-1
NM_052988 CDK10 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs258322 2.00E-23 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_052988 CDK10 19578364 http://www.ncbi.nlm.nih.gov/pubmed/19578364 Melanoma rs258322 3.00E-27 Genome-wide association study identifies three loci associated with melanoma risk. NHGRI|-1
NM_052997 ANKRD30A 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Sphingomyelins rs1148259 3.00E-09 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_052997 ANKRD30A 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Indices rs1200821 6.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_053002 MED12L 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs7637803 6.71E-06 NBL-GWAS version 1 dbGaP|2845
NM_053004 GNB1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs9306226 9.50E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_053034 ANTXR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6710260 2.53E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_053035 MRPS33 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs528957 7.80E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_053035 MRPS33 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs557962 5.86E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_053042 ZNF518B 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Bone Density rs9291683 2.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_053046 EGLN2 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs3733829 1.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_053055 THEM4 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs10788819 2.00E-08 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_053056 CCND1 21131975 http://www.ncbi.nlm.nih.gov/pubmed/21131975 "Carcinoma, Renal Cell" rs7105934 8.00E-14 Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3. NHGRI|-1
NM_053056 CCND1 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs614367 3.00E-15 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_053064 GNG2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs10133203 1.06E-05 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_053276 VIT 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11691187 4.77E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_053279 FAM167A 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs7812879 2.00E-24 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_053279 FAM167A 19503088 http://www.ncbi.nlm.nih.gov/pubmed/19503088 "Arthritis, Rheumatoid" rs2736340 6.00E-09 "REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis." NHGRI|-1
NM_053279 FAM167A 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs2736340 3.00E-07 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_053279 FAM167A 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs13277113 1.00E-10 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_053281 DACH2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs242849 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_053283 DCD 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs1153188 2.00E-07 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_054022 GOSR2 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs17608766 5.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_054028 AMAC1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1032061 1.55E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_054034 FN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1250255 3.21E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_054111 IP6K3 20558539 http://www.ncbi.nlm.nih.gov/pubmed/20558539 Phosphorus rs9469578 1.00E-11 Common genetic variants associate with serum phosphorus concentration. NHGRI|-1
NM_054114 TAGAP 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1738074 3.00E-15 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_054114 TAGAP 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs1738074 7.00E-08 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_054114 TAGAP 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs212388 2.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_054114 TAGAP 21298027 http://www.ncbi.nlm.nih.gov/pubmed/21298027 Intestinal Diseases rs212388 2.00E-10 "A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease." NHGRI|-1
NM_054114 TAGAP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2016588 1.29E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_054114 TAGAP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2057061 3.47E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_057158 DUSP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs601962 5.33E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_057158 DUSP4 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, HDL" rs10091038 3.00E-08 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_057159 LPAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1536435 1.10E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_057159 LPAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1536435 9.93E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_057159 LPAR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs509276 2.53E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_057162 KLHL4 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs2710057 1.00E-06 New sequence variants associated with bone mineral density. NHGRI|-1
NM_057169 GIT2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs2292354 7.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_057169 GIT2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11068997 7.24E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_057170 GIT2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs2292354 7.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_057170 GIT2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11068997 7.24E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_057176 BSND 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs11206510 1.00E-10 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_057176 BSND 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs11206510 4.00E-11 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_057176 BSND 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs11206510 4.00E-08 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_057176 BSND 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs11206510 9.00E-08 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_057176 BSND 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs11206510 1.00E-08 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_057177 PARD3B 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs2335704 2.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_057177 PARD3B 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2276677 8.56E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_057177 PARD3B 18471798 http://www.ncbi.nlm.nih.gov/pubmed/18471798 "Osteoarthritis, Knee" rs1207421 6.00E-06 Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis. NHGRI|-1
NM_057177 PARD3B 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs11884476 3.00E-09 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_057177 PARD3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7421114 9.89E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_057179 TWIST2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2878083 4.21E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_057179 TWIST2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12692245 4.48E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_057179 TWIST2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9798281 3.87E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_057182 CCNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs184583 2.90E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_057182 CCNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs184583 3.72E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_057182 CCNE1 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs8102137 2.00E-11 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_058164 OLFM2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1862471 2.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_058172 ANTXR2 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs4389526 9.00E-08 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_058172 ANTXR2 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs4333130 9.00E-08 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_058174 COL6A2 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs4293630 7.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_058175 COL6A2 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs4293630 7.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_058176 HDAC9 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs615545 5.89E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_058240 SLC8A3 21602797 http://www.ncbi.nlm.nih.gov/pubmed/21602797 Cystic Fibrosis rs12883884 8.00E-06 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. NHGRI|-1
NM_058246 DNAJB6 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs10227331 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_058246 DNAJB6 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Blood Pressure rs2527866 3.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_078467 CDKN1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs236449 9.40E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_078467 CDKN1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs236448 9.39E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_078467 CDKN1A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs1321311 3.00E-10 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_078467 CDKN1A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9470361 3.00E-27 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_078476 BTN2A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs13195509 1.17E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_078476 BTN2A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs13195509 7.66E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_078476 BTN2A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs9358946 1.12E-08 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_078476 BTN2A1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs16891725 6.05E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_078481 CD97 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs4528684 1.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_078487 CDKN2B 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1063192 4.00E-15 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_078626 CDKN2C 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs17391905 3.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_079837 BANP 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs4843747 2.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_079837 BANP 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs12447690 6.00E-22 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_079837 BANP 20485516 http://www.ncbi.nlm.nih.gov/pubmed/20485516 Cornea rs12447690 9.00E-11 Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. NHGRI|-1
NM_080385 CPA5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4731688 1.52E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_080390 TCEAL2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs5944858 1.12E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_080422 PTPN2 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs1893217 5.00E-12 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_080422 PTPN2 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1893217 3.00E-10 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_080422 PTPN2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs1893217 4.00E-15 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_080422 PTPN2 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs2847281 2.00E-08 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_080422 PTPN2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs2542151 2.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_080422 PTPN2 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs2542151 3.00E-08 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_080422 PTPN2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2542151 5.00E-17 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_080422 PTPN2 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs2542151 1.00E-14 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_080422 PTPN2 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs2542151 9.00E-08 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_080423 PTPN2 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs1893217 5.00E-12 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_080423 PTPN2 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1893217 3.00E-10 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_080423 PTPN2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs1893217 4.00E-15 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_080423 PTPN2 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs2847281 2.00E-08 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_080423 PTPN2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs2542151 2.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_080423 PTPN2 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs2542151 3.00E-08 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_080423 PTPN2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2542151 5.00E-17 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_080423 PTPN2 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs2542151 1.00E-14 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_080423 PTPN2 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs2542151 9.00E-08 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_080425 GNAS 21046636 http://www.ncbi.nlm.nih.gov/pubmed/21046636 Brain Waves rs13831 6.00E-06 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. NHGRI|-1
NM_080426 GNAS 21046636 http://www.ncbi.nlm.nih.gov/pubmed/21046636 Brain Waves rs13831 6.00E-06 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. NHGRI|-1
NM_080476 PIGU 18488026 http://www.ncbi.nlm.nih.gov/pubmed/18488026 Melanoma rs910873 1.00E-15 Common sequence variants on 20q11.22 confer melanoma susceptibility. NHGRI|-1
NM_080491 GAB2 17553421 http://www.ncbi.nlm.nih.gov/pubmed/17553421 Alzheimer Disease rs2373115 1.00E-10 GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers. NHGRI|-1
NM_080491 GAB2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs10899489 8.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_080538 COLQ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12495710 4.38E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_080539 COLQ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12495710 4.38E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_080594 RNPS1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9796949 5.84E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_080596 HIST1H2AH 19571811 http://www.ncbi.nlm.nih.gov/pubmed/19571811 Schizophrenia rs13194053 1.00E-08 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. NHGRI|-1
NM_080596 HIST1H2AH 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs13194053 1.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_080597 OSBPL1A 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Sex Hormone-Binding Globulin rs9635963 2.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_080597 OSBPL1A 20548944 http://www.ncbi.nlm.nih.gov/pubmed/20548944 Osteoporosis rs7227401 4.00E-07 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. NHGRI|-1
NM_080598 BAT1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3115537 2.46E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_080598 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3093978 8.82E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_080598 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3093948 8.72E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_080598 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3093976 1.03E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_080598 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3130057 1.07E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_080598 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2734583 5.29E-68 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_080598 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3130058 6.23E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_080598 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2516393 8.82E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_080598 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2239709 4.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_080598 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2251824 5.97E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_080610 CST9L 17903292 http://www.ncbi.nlm.nih.gov/pubmed/17903292 Cystatin C rs1158167 9.00E-09 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_080612 GAB3 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2664170 8.00E-09 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_080617 CBLN4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6014573 4.04E-05 NBL-GWAS version 2 dbGaP|2895
NM_080617 CBLN4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6069551 9.25E-05 NBL-GWAS version 2 dbGaP|2895
NM_080617 CBLN4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6024619 4.54E-05 NBL-GWAS version 2 dbGaP|2895
NM_080617 CBLN4 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs6092078 3.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_080629 COL11A1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1415363 5.62E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_080629 COL11A1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Fibrinogen rs10874639 3.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_080630 COL11A1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1415363 5.62E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_080630 COL11A1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Fibrinogen rs10874639 3.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_080631 VPS41 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs11984145 6.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_080631 VPS41 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs859522 3.41E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_080650 ATPBD4 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1510385 1.43E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_080650 ATPBD4 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs4923705 2.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_080650 ATPBD4 20673876 http://www.ncbi.nlm.nih.gov/pubmed/20673876 "Depressive Disorder, Major" rs10520045 7.00E-06 "Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression." NHGRI|-1
NM_080650 ATPBD4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs16962759 6.38E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_080650 ATPBD4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs16962759 8.28E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_080650 ATPBD4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4130461 4.52E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_080650 ATPBD4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs8028529 1.51E-06 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_080650 ATPBD4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4459505 1.12E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_080653 ATP6V1E2 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs12623288 3.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_080653 ATP6V1E2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs2346177 2.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_080671 KCNE4 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs12621643 3.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_080671 KCNE4 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs1440072 4.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_080671 KCNE4 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs1440072 8.00E-07 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_080676 MACROD2 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs6079395 7.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_080676 MACROD2 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs6110278 4.00E-07 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_080676 MACROD2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6079482 4.19E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_080676 MACROD2 20663923 http://www.ncbi.nlm.nih.gov/pubmed/20663923 Autistic Disorder rs4141463 4.00E-08 A genome-wide scan for common alleles affecting risk for autism. NHGRI|-1
NM_080676 MACROD2 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs6110577 5.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_080676 MACROD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6043422 8.97E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_080676 MACROD2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6043600 6.18E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_080679 COL11A2 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs2254287 5.00E-08 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_080680 COL11A2 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs2254287 5.00E-08 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_080681 COL11A2 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs2254287 5.00E-08 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_080686 BAT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2242660 3.94E-109 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_080686 BAT2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2242660 8.73E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_080686 BAT2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3115663 6.66E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_080686 BAT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs1046089 1.28E-124 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_080686 BAT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1046089 2.40E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_080686 BAT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1046089 1.30E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_080686 BAT2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1046089 3.79E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_080686 BAT2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs11229 5.55E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_080686 BAT2 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2736177 3.15E-23 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_080687 UPF3A 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7316983 1.05E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_080702 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1077393 3.83E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_080702 BAT3 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs760293 9.72E-20 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_080702 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs805303 2.79E-119 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_080702 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs805303 1.25E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_080702 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3130050 1.52E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_080702 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3117583 3.33E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_080702 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3117582 2.62E-83 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_080702 BAT3 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs3117582 4.00E-10 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_080702 BAT3 18978787 http://www.ncbi.nlm.nih.gov/pubmed/18978787 Lung Neoplasms rs3117582 5.00E-10 Common 5p15.33 and 6p21.33 variants influence lung cancer risk. NHGRI|-1
NM_080702 BAT3 19836008 http://www.ncbi.nlm.nih.gov/pubmed/19836008 Lung Neoplasms rs3117582 5.00E-12 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. NHGRI|-1
NM_080702 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3117582 4.53E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_080703 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs1077393 3.83E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_080703 BAT3 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs760293 9.72E-20 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_080703 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs805303 2.79E-119 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_080703 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs805303 1.25E-09 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_080703 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3130050 1.52E-71 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_080703 BAT3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3117583 3.33E-16 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_080703 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3117582 2.62E-83 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_080703 BAT3 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs3117582 4.00E-10 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_080703 BAT3 18978787 http://www.ncbi.nlm.nih.gov/pubmed/18978787 Lung Neoplasms rs3117582 5.00E-10 Common 5p15.33 and 6p21.33 variants influence lung cancer risk. NHGRI|-1
NM_080703 BAT3 19836008 http://www.ncbi.nlm.nih.gov/pubmed/19836008 Lung Neoplasms rs3117582 5.00E-12 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. NHGRI|-1
NM_080703 BAT3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3117582 4.53E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_080717 TBX5 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs883079 1.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_080717 TBX5 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3825214 1.00E-07 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_080717 TBX5 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3825214 3.00E-12 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_080717 TBX5 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3825214 3.00E-13 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_080717 TBX5 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1946295 7.87E-06 NBL-GWAS version 1 dbGaP|2845
NM_080718 TBX5 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs883079 1.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_080718 TBX5 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3825214 1.00E-07 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_080718 TBX5 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3825214 3.00E-12 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_080718 TBX5 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3825214 3.00E-13 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_080718 TBX5 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1946295 7.87E-06 NBL-GWAS version 1 dbGaP|2845
NM_080722 ADAMTS14 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs7092269 5.29E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_080722 ADAMTS14 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs1816002 8.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_080723 NRSN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12210008 4.70E-05 NBL-GWAS version 2 dbGaP|2895
NM_080723 NRSN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2176933 2.09E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_080723 NRSN1 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs6922632 4.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_080732 EGLN2 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs3733829 1.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_080742 B3GAT2 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs11968814 9.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_080743 SRSF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs10223547 1.93E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_080751 TMC2 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs6049839 8.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_080759 DACH1 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Cystatin C rs626277 3.00E-11 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_080759 DACH1 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs9572423 9.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_080759 DACH1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7317253 2.51E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_080759 DACH1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs9592783 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_080760 DACH1 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Cystatin C rs626277 3.00E-11 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_080760 DACH1 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs9572423 9.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_080760 DACH1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7317253 2.51E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_080760 DACH1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs9592783 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_080792 SIRPA 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs6136489 8.00E-11 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_080792 SIRPA 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs6045676 3.00E-08 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_080794 MRPL39 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs17001239 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_080798 COL13A1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs7077164 7.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_080798 COL13A1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1227756 2.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_080800 COL13A1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs7077164 7.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_080800 COL13A1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1227756 2.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_080801 COL13A1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs7077164 7.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_080801 COL13A1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1227756 2.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_080802 COL13A1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs7077164 7.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_080802 COL13A1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1227756 2.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_080805 COL13A1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs7077164 7.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_080805 COL13A1 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1227756 2.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_080816 SIRPG 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs2281808 1.00E-11 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_080819 GPR78 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs1949733 8.00E-07 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_080826 ISM1 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs1223271 5.00E-06 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_080868 ASB17 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Personality rs12753569 8.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_080870 DPCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3132580 1.66E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_080870 DPCR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs3132580 2.59E-13 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_080870 DPCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2240804 2.09E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_080870 DPCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2240803 8.19E-13 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_080870 DPCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844697 6.16E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_080870 DPCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3095089 1.03E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_080870 DPCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3095089 2.09E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_080870 DPCR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844680 6.06E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_080916 DGUOK 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs6546886 3.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_080918 DGUOK 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs6546886 3.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_080921 PTPRC 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs12127588 7.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_080923 PTPRC 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs12127588 7.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_080927 DCBLD2 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs2670321 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_080927 DCBLD2 20686651 http://www.ncbi.nlm.nih.gov/pubmed/20686651 Cornea rs13070584 2.00E-06 Association of variants at UMOD with chronic kidney disease and kidney stones-role of age and comorbid diseases. NHGRI|-1
NM_101395 DYRK1A 21364930 http://www.ncbi.nlm.nih.gov/pubmed/21364930 HIV-1 rs12483205 5.00E-06 Genome-wide association study identifies single nucleotide polymorphism in DYRK1A associated with replication of HIV-1 in monocyte-derived macrophages. NHGRI|-1
NM_101395 DYRK1A 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs2835810 6.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_130384 ATRIP 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs9876781 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_130385 MRVI1 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7940646 1.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_130385 MRVI1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2018368 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_130385 MRVI1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11042937 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_130386 COLEC12 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs7226677 4.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_130386 COLEC12 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs7226677 7.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_130391 PTPRD 18660810 http://www.ncbi.nlm.nih.gov/pubmed/18660810 Restless Legs Syndrome rs1975197 6.00E-09 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. NHGRI|-1
NM_130391 PTPRD 20174558 http://www.ncbi.nlm.nih.gov/pubmed/20174558 "Diabetes Mellitus, Type 2" rs17584499 9.00E-10 A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. NHGRI|-1
NM_130391 PTPRD 18660810 http://www.ncbi.nlm.nih.gov/pubmed/18660810 Restless Legs Syndrome rs4626664 6.00E-10 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. NHGRI|-1
NM_130391 PTPRD 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs2475335 9.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_130391 PTPRD 21647700 http://www.ncbi.nlm.nih.gov/pubmed/21647700 "Diabetes Mellitus, Type 2" rs649891 6.00E-06 "Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals." NHGRI|-1
NM_130391 PTPRD 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Braces rs1535480 4.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_130391 PTPRD 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7044355 1.00E-07 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_130391 PTPRD 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10815798 6.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_130392 PTPRD 18660810 http://www.ncbi.nlm.nih.gov/pubmed/18660810 Restless Legs Syndrome rs1975197 6.00E-09 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. NHGRI|-1
NM_130392 PTPRD 20174558 http://www.ncbi.nlm.nih.gov/pubmed/20174558 "Diabetes Mellitus, Type 2" rs17584499 9.00E-10 A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. NHGRI|-1
NM_130392 PTPRD 18660810 http://www.ncbi.nlm.nih.gov/pubmed/18660810 Restless Legs Syndrome rs4626664 6.00E-10 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. NHGRI|-1
NM_130392 PTPRD 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs2475335 9.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_130392 PTPRD 21647700 http://www.ncbi.nlm.nih.gov/pubmed/21647700 "Diabetes Mellitus, Type 2" rs649891 6.00E-06 "Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals." NHGRI|-1
NM_130392 PTPRD 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Braces rs1535480 4.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_130392 PTPRD 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7044355 1.00E-07 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_130392 PTPRD 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10815798 6.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_130393 PTPRD 18660810 http://www.ncbi.nlm.nih.gov/pubmed/18660810 Restless Legs Syndrome rs1975197 6.00E-09 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. NHGRI|-1
NM_130393 PTPRD 20174558 http://www.ncbi.nlm.nih.gov/pubmed/20174558 "Diabetes Mellitus, Type 2" rs17584499 9.00E-10 A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. NHGRI|-1
NM_130393 PTPRD 18660810 http://www.ncbi.nlm.nih.gov/pubmed/18660810 Restless Legs Syndrome rs4626664 6.00E-10 PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. NHGRI|-1
NM_130393 PTPRD 20522523 http://www.ncbi.nlm.nih.gov/pubmed/20522523 "Epilepsies, Partial" rs2475335 9.00E-06 Common genetic variation and susceptibility to partial epilepsies: a genome-wide association study. NHGRI|-1
NM_130393 PTPRD 21647700 http://www.ncbi.nlm.nih.gov/pubmed/21647700 "Diabetes Mellitus, Type 2" rs649891 6.00E-06 "Genome-wide association and meta-analysis in populations from Starr County, Texas, and Mexico City identify type 2 diabetes susceptibility loci and enrichment for expression quantitative trait loci in top signals." NHGRI|-1
NM_130393 PTPRD 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Braces rs1535480 4.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_130393 PTPRD 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs7044355 1.00E-07 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_130393 PTPRD 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10815798 6.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_130436 DYRK1A 21364930 http://www.ncbi.nlm.nih.gov/pubmed/21364930 HIV-1 rs12483205 5.00E-06 Genome-wide association study identifies single nucleotide polymorphism in DYRK1A associated with replication of HIV-1 in monocyte-derived macrophages. NHGRI|-1
NM_130436 DYRK1A 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs2835810 6.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_130438 DYRK1A 21364930 http://www.ncbi.nlm.nih.gov/pubmed/21364930 HIV-1 rs12483205 5.00E-06 Genome-wide association study identifies single nucleotide polymorphism in DYRK1A associated with replication of HIV-1 in monocyte-derived macrophages. NHGRI|-1
NM_130438 DYRK1A 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs2835810 6.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_130439 MXI1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs716595 8.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_130439 MXI1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7917994 8.56E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_130439 MXI1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7921757 8.56E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_130440 PTPRF 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12069733 8.59E-08 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_130442 ELMO1 17653210 http://www.ncbi.nlm.nih.gov/pubmed/17653210 Diabetic Nephropathies rs741301 8.00E-06 Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population. NHGRI|-1
NM_130442 ELMO1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs10488031 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_130442 ELMO1 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs4723619 3.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_130442 ELMO1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs6974491 2.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_130442 ELMO1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs6974491 4.00E-08 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_130442 ELMO1 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs11984075 5.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_130445 COL18A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs957795 1.25E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_130445 COL18A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs957794 1.01E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_130463 ATP6V1G2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2251824 5.97E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_130463 ATP6V1G2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071593 4.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_130463 ATP6V1G2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2523503 5.59E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_130466 UBE3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7298565 6.93E-05 NBL-GWAS version 2 dbGaP|2895
NM_130466 UBE3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7486178 3.90E-06 NBL-GWAS version 2 dbGaP|2895
NM_130469 JDP2 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs7155603 1.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_130470 MADD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs4752977 9.72E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_130470 MADD 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs7944584 2.00E-18 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_130471 MADD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs4752977 9.72E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_130471 MADD 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs7944584 2.00E-18 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_130472 MADD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs4752977 9.72E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_130472 MADD 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs7944584 2.00E-18 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_130473 MADD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs4752977 9.72E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_130473 MADD 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs7944584 2.00E-18 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_130474 MADD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs4752977 9.72E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_130474 MADD 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs7944584 2.00E-18 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_130475 MADD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs4752977 9.72E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_130475 MADD 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs7944584 2.00E-18 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_130476 MADD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs4752977 9.72E-06 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_130476 MADD 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs7944584 2.00E-18 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_130768 ASZ1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs7808424 1.00E-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_130773 CNTNAP5 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs1367248 3.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_130773 CNTNAP5 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs17727261 5.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_130773 CNTNAP5 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs2901331 6.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_130773 CNTNAP5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6710520 2.18E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_130773 CNTNAP5 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs10207651 7.81E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_130773 CNTNAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4241112 9.25E-06 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_130773 CNTNAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17779391 3.76E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_130773 CNTNAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs11685781 1.31E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_130773 CNTNAP5 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs1527243 1.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_130773 CNTNAP5 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs17367118 9.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_130782 RGS18 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1327872 3.15E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_130782 RGS18 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs17379742 7.67E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_130782 RGS18 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs2053302 4.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_130782 RGS18 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs10801047 3.00E-08 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_130791 WWOX 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs2059238 3.00E-06 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_130791 WWOX 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs17706989 1.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_130791 WWOX 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs2859631 1.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_130791 WWOX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs8047442 2.97E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_130791 WWOX 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs9923451 8.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_130791 WWOX 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1109934 3.45E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_130791 WWOX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7200634 7.11E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_130797 DPP6 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs6464375 4.00E-07 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_130797 DPP6 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10260404 3.00E-06 A genome-wide association study of sporadic ALS in a homogenous Irish population. NHGRI|-1
NM_130797 DPP6 18987618 http://www.ncbi.nlm.nih.gov/pubmed/18987618 Amyotrophic Lateral Sclerosis rs10260404 3.00E-06 Screening for replication of genome-wide SNP associations in sporadic ALS. NHGRI|-1
NM_130797 DPP6 18084291 http://www.ncbi.nlm.nih.gov/pubmed/18084291 Amyotrophic Lateral Sclerosis rs10260404 5.00E-08 Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis. NHGRI|-1
NM_130797 DPP6 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6952728 5.15E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_130808 CPNE4 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs6775745 2.00E-07 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_130809 PRRC1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs374499 8.86E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_130838 UBE3A 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs17636733 2.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_130838 UBE3A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2930629 5.39E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_130839 UBE3A 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs17636733 2.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_130839 UBE3A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2930629 5.39E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_130840 ATP6V0A4 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs3800569 6.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_130840 ATP6V0A4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs366193 8.90E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_130841 ATP6V0A4 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs3800569 6.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_130841 ATP6V0A4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs366193 8.90E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_130842 PTPRN2 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs6459804 8.00E-06 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_130842 PTPRN2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs10227331 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_130843 PTPRN2 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs6459804 8.00E-06 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_130843 PTPRN2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs10227331 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_130844 WWOX 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs2059238 3.00E-06 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_130844 WWOX 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs17706989 1.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_130844 WWOX 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs2859631 1.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_130844 WWOX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs8047442 2.97E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_130844 WWOX 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs9923451 8.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_130844 WWOX 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1109934 3.45E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_130844 WWOX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7200634 7.11E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_130846 PTPRR 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2470378 6.28E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_130850 BMP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12431733 1.52E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_130850 BMP4 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs12431733 3.00E-06 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_130850 BMP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8005200 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_130850 BMP4 19011631 http://www.ncbi.nlm.nih.gov/pubmed/19011631 Colorectal Neoplasms rs4444235 8.00E-10 Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. NHGRI|-1
NM_130851 BMP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12431733 1.52E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_130851 BMP4 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs12431733 3.00E-06 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_130851 BMP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8005200 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_130851 BMP4 19011631 http://www.ncbi.nlm.nih.gov/pubmed/19011631 Colorectal Neoplasms rs4444235 8.00E-10 Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer. NHGRI|-1
NM_130853 PTPRS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4807016 8.29E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_130854 PTPRS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4807016 8.29E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_130855 PTPRS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4807016 8.29E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_130897 DYNLRB2 19151714 http://www.ncbi.nlm.nih.gov/pubmed/19151714 Obesity rs1424233 4.00E-13 Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations. NHGRI|-1
NM_130897 DYNLRB2 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs17767419 9.00E-15 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_130897 DYNLRB2 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs3813579 4.00E-10 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_130901 OTUD7A 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs2125623 1.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_133170 PTPRT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs2206426 9.22E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_133170 PTPRT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs941796 1.79E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_133170 PTPRT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs6016596 6.01E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_133170 PTPRT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs12480143 2.99E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_133170 PTPRT 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2866823 1.63E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_133177 PTPRU 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1932397 7.14E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_133177 PTPRU 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9286938 9.14E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_133177 PTPRU 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs4949526 4.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_133177 PTPRU 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11580589 2.48E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_133177 PTPRU 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs910696 3.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_133177 PTPRU 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs2180233 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_133178 PTPRU 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1932397 7.14E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_133178 PTPRU 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9286938 9.14E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_133178 PTPRU 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs4949526 4.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_133178 PTPRU 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11580589 2.48E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_133178 PTPRU 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs910696 3.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_133178 PTPRU 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs2180233 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_133181 EPS8L3 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs10494112 7.00E-35 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_133181 EPS8L3 20436471 http://www.ncbi.nlm.nih.gov/pubmed/20436471 Osteitis Deformans rs484959 5.00E-24 "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone." NHGRI|-1
NM_133181 EPS8L3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs525566 5.88E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_133262 ATP6V1G3 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs12127588 7.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_133263 PPARGC1B 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs32579 4.00E-06 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_133265 AMOT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs547425 1.12E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_133265 AMOT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs648170 7.30E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_133326 ATP6V1G3 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs12127588 7.00E-10 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_133373 PLCD3 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs12946454 1.00E-08 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_133375 DIS3L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6494562 9.58E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_133376 ITGB1 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs11009175 5.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_133378 TTN 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs12476289 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_133379 TTN 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs12476289 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_133432 TTN 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs12476289 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_133437 TTN 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs12476289 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_133448 TMEM132D 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs12371373 7.18E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_133448 TMEM132D 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4759966 3.10E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_133458 ZFP90 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs1728785 3.00E-08 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_133458 ZFP90 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs17689437 1.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_133458 ZFP90 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6499188 4.00E-08 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_133459 CCBE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1944980 5.75E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_133463 AMZ1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs798544 7.00E-15 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_133464 ZNF483 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs10980926 4.00E-11 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_133468 BMPER 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1362927 2.87E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_133482 RAD50 20159242 http://www.ncbi.nlm.nih.gov/pubmed/20159242 Asthma rs2244012 3.00E-07 Genome-wide association study of asthma identifies RAD50-IL13 and HLA-DR/DQ regions. NHGRI|-1
NM_133482 RAD50 18846228 http://www.ncbi.nlm.nih.gov/pubmed/18846228 Immunoglobulin E rs2040704 4.00E-08 Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus. NHGRI|-1
NM_133484 TANK 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs10192369 9.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_133484 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6432628 9.13E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133484 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13034284 1.85E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133484 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9967749 8.13E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133484 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11681327 4.77E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133484 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7603576 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133484 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2551691 9.03E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_133484 TANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs197275 4.42E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_133503 DCN 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10777317 5.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_133503 DCN 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Cholesterol rs10777332 5.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_133503 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11106325 1.82E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_133503 DCN 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs17019682 2.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_133503 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4356270 4.44E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133503 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4499040 6.57E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133503 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11106345 6.02E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133504 DCN 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10777317 5.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_133504 DCN 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Cholesterol rs10777332 5.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_133504 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11106325 1.82E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_133504 DCN 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs17019682 2.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_133504 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4356270 4.44E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133504 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4499040 6.57E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133504 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11106345 6.02E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133505 DCN 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10777317 5.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_133505 DCN 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Cholesterol rs10777332 5.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_133505 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11106325 1.82E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_133505 DCN 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs17019682 2.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_133505 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4356270 4.44E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133505 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4499040 6.57E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133505 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11106345 6.02E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133506 DCN 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10777317 5.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_133506 DCN 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Cholesterol rs10777332 5.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_133506 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11106325 1.82E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_133506 DCN 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs17019682 2.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_133506 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4356270 4.44E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133506 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4499040 6.57E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133506 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11106345 6.02E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133507 DCN 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10777317 5.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_133507 DCN 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Cholesterol rs10777332 5.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_133507 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11106325 1.82E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_133507 DCN 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs17019682 2.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_133507 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4356270 4.44E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133507 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4499040 6.57E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133507 DCN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11106345 6.02E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_133509 RAD51L1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs911263 2.00E-11 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_133509 RAD51L1 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs1956529 3.00E-08 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_133509 RAD51L1 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs999737 2.00E-07 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_133510 RAD51L1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs911263 2.00E-11 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_133510 RAD51L1 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs1956529 3.00E-08 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_133510 RAD51L1 19330030 http://www.ncbi.nlm.nih.gov/pubmed/19330030 Breast Neoplasms rs999737 2.00E-07 A multistage genome-wide association study in breast cancer identifies two new risk alleles at 1p11.2 and 14q24.1 (RAD51L1). NHGRI|-1
NM_133625 SYN2 21314694 http://www.ncbi.nlm.nih.gov/pubmed/21314694 Alcoholism rs6777876 4.00E-07 Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample. NHGRI|-1
NM_133633 SYN3 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Macular Degeneration rs9621532 1.00E-11 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_133633 SYN3 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs9621532 2.00E-15 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_133633 SYN3 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Macular Degeneration rs9621532 4.00E-09 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_133636 HELQ 21437268 http://www.ncbi.nlm.nih.gov/pubmed/21437268 Head and Neck Neoplasms rs1494961 1.00E-08 A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. NHGRI|-1
NM_133642 LARGE 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs130575 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_133646 ZAK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs10187560 8.98E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_133650 SYNE1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs2673776 8.05E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_133650 SYNE1 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs17082664 1.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_133650 SYNE1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs17082664 4.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_133650 SYNE1 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs7747960 9.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_133650 SYNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2623963 7.61E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_133650 SYNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7745725 1.87E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_133650 SYNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1358317 1.61E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_133650 SYNE1 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs1322512 8.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_134260 RORA 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs3743266 8.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_134260 RORA 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs340029 4.00E-09 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_134260 RORA 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs3784609 3.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_134260 RORA 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs11071559 1.00E-07 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_134260 RORA 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs12912233 6.00E-07 Genome-wide association scan of trait depression. NHGRI|-1
NM_134260 RORA 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs809736 8.00E-06 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_134261 RORA 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs3743266 8.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_134261 RORA 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs340029 4.00E-09 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_134261 RORA 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs3784609 3.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_134261 RORA 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs11071559 1.00E-07 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_134261 RORA 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs12912233 6.00E-07 Genome-wide association scan of trait depression. NHGRI|-1
NM_134261 RORA 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs809736 8.00E-06 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_134262 RORA 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs3743266 8.00E-07 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_134262 RORA 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs340029 4.00E-09 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_134262 RORA 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs3784609 3.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_134262 RORA 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs11071559 1.00E-07 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_134262 RORA 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs12912233 6.00E-07 Genome-wide association scan of trait depression. NHGRI|-1
NM_134262 RORA 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs809736 8.00E-06 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NM_134269 SMTN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs5753454 6.91E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_134270 SMTN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs5753454 6.91E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_134325 SLC26A9 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Antipsychotic Agents rs11240594 1.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_134424 RAD52 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6413436 8.95E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_134431 SLCO1A2 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs11568563 7.00E-08 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_134433 RFX2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11880706 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_134440 RFXANK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10896 1.65E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_134447 C19orf2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs184583 2.90E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_134447 C19orf2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs184583 3.72E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_134470 IL1RAP 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs9290936 4.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_134470 IL1RAP 18385676 http://www.ncbi.nlm.nih.gov/pubmed/18385676 Lung Neoplasms rs7626795 8.00E-06 Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1. NHGRI|-1
NM_138282 ATP6V1G2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2251824 5.97E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_138282 ATP6V1G2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071593 4.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_138282 ATP6V1G2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2523503 5.59E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_138283 CSTL1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs3746736 2.25E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_138288 C14orf147 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1680730 1.71E-05 NBL-GWAS version 2 dbGaP|2895
NM_138295 PKD1L1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs12670472 2.77E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_138316 PANK1 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Insulin rs11185790 3.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_138316 PANK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Insulin rs11185790 9.73E-05 Genomewide association analysis of insulin (INS) in a birth cohort from a founder population dbGaP|2901
NM_138317 KCNK10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12434331 6.34E-05 NBL-GWAS version 2 dbGaP|2895
NM_138317 KCNK10 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs17124581 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_138318 KCNK10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12434331 6.34E-05 NBL-GWAS version 2 dbGaP|2895
NM_138318 KCNK10 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs17124581 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_138319 PCSK6 21051773 http://www.ncbi.nlm.nih.gov/pubmed/21051773 Functional Laterality rs11855415 2.00E-08 PCSK6 is associated with handedness in individuals with dyslexia. NHGRI|-1
NM_138320 PCSK6 21051773 http://www.ncbi.nlm.nih.gov/pubmed/21051773 Functional Laterality rs11855415 2.00E-08 PCSK6 is associated with handedness in individuals with dyslexia. NHGRI|-1
NM_138321 PCSK6 21051773 http://www.ncbi.nlm.nih.gov/pubmed/21051773 Functional Laterality rs11855415 2.00E-08 PCSK6 is associated with handedness in individuals with dyslexia. NHGRI|-1
NM_138322 PCSK6 21051773 http://www.ncbi.nlm.nih.gov/pubmed/21051773 Functional Laterality rs11855415 2.00E-08 PCSK6 is associated with handedness in individuals with dyslexia. NHGRI|-1
NM_138323 PCSK6 21051773 http://www.ncbi.nlm.nih.gov/pubmed/21051773 Functional Laterality rs11855415 2.00E-08 PCSK6 is associated with handedness in individuals with dyslexia. NHGRI|-1
NM_138324 PCSK6 21051773 http://www.ncbi.nlm.nih.gov/pubmed/21051773 Functional Laterality rs11855415 2.00E-08 PCSK6 is associated with handedness in individuals with dyslexia. NHGRI|-1
NM_138325 PCSK6 21051773 http://www.ncbi.nlm.nih.gov/pubmed/21051773 Functional Laterality rs11855415 2.00E-08 PCSK6 is associated with handedness in individuals with dyslexia. NHGRI|-1
NM_138326 ACMSD 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs6710823 7.00E-09 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_138335 GNPDA2 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs10938397 3.00E-16 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_138335 GNPDA2 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10938397 4.00E-31 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_138335 GNPDA2 21700879 http://www.ncbi.nlm.nih.gov/pubmed/21700879 Adiponectin rs10517133 5.00E-06 Novel Locus FER Is Associated With Serum HMW Adiponectin Levels. NHGRI|-1
NM_138346 KIAA2013 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6682554 7.16E-05 NBL-GWAS version 2 dbGaP|2895
NM_138356 SHF 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2162246 3.44E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_138356 SHF 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2292468 1.76E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_138356 SHF 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1648307 1.69E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_138369 BOD1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs359457 3.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_138369 BOD1 19165155 http://www.ncbi.nlm.nih.gov/pubmed/19165155 Adiponectin rs7722022 9.00E-06 Genome-wide linkage and association analyses to identify genes influencing adiponectin levels: the GEMS Study. NHGRI|-1
NM_138369 BOD1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs889014 9.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_138370 PKDCC 19961619 http://www.ncbi.nlm.nih.gov/pubmed/19961619 Nonalcoholic Fatty Liver Disease rs4952590 2.00E-06 A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS). NHGRI|-1
NM_138370 PKDCC 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs11887431 1.24E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_138371 FAM113B 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs11610206 3.00E-07 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NM_138375 CABLES1 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs11082304 6.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_138375 CABLES1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs4800148 4.00E-09 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_138375 CABLES1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs4369779 3.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_138375 CABLES1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs4369779 6.86E-04 Genome-wide association between genotype and incident stroke in participants of primarily self-described European ancestry dbGaP|2886
NM_138379 TIMD4 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs1501908 1.00E-11 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_138386 NAF1 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs6840361 4.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_138389 FAM114A1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs13150445 4.34E-07 NBL-GWAS version 1 dbGaP|2845
NM_138399 TMEM44 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs789852 7.00E-07 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_138410 CMTM7 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs12638540 3.00E-07 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_138426 GLCCI1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs9648623 4.15E-05 NBL-GWAS version 2 dbGaP|2895
NM_138426 GLCCI1 21216879 http://www.ncbi.nlm.nih.gov/pubmed/21216879 Insulin-Like Growth Factor I rs7780564 4.00E-07 A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. NHGRI|-1
NM_138436 C8orf40 20418888 http://www.ncbi.nlm.nih.gov/pubmed/20418888 Smoking rs6474412 1.00E-08 Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. NHGRI|-1
NM_138447 ZNF689 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs7186852 3.00E-07 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_138447 ZNF689 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs7197475 3.00E-08 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_138448 ACYP2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs1559040 4.00E-08 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_138457 FOXP4 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs1983891 8.00E-08 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_138473 SP1 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs10876432 1.00E-07 New sequence variants associated with bone mineral density. NHGRI|-1
NM_138484 SGOL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6776153 9.43E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_138484 SGOL1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs11720452 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_138484 SGOL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1395993 3.49E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_138493 C6orf129 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs904251 7.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_138494 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Anthropometry rs7792939 5.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_138494 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weight rs7792939 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_138494 ZNF655 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weights and Measures rs7792939 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_138554 TLR4 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Stomach Neoplasms rs876347 2.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_138554 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1335258 1.77E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_138554 TLR4 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs1572299 4.00E-06 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_138554 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10984107 4.62E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_138554 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11789399 4.30E-06 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_138554 TLR4 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11789399 6.00E-09 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_138554 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11789399 1.60E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_138554 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11789407 1.69E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_138554 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11789407 2.17E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_138554 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10759986 2.89E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_138554 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10733631 2.07E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_138554 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10759987 3.57E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_138554 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7866602 5.24E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_138554 TLR4 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12237612 9.36E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_138559 BCL11A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7593947 8.46E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_138559 BCL11A 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 Fetal Hemoglobin rs1427407 6.00E-31 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_138559 BCL11A 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Nonalcoholic Fatty Liver Disease rs766432 1.00E-10 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_138559 BCL11A 18245381 http://www.ncbi.nlm.nih.gov/pubmed/18245381 Fetal Hemoglobin rs11886868 7.00E-35 Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. NHGRI|-1
NM_138559 BCL11A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7592415 1.56E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_138559 BCL11A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17552189 8.46E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_138559 BCL11A 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs17552189 4.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_138559 BCL11A 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs991964 9.00E-06 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_138559 BCL11A 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs887912 2.00E-12 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_138559 BCL11A 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs10490113 5.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_138559 BCL11A 21493818 http://www.ncbi.nlm.nih.gov/pubmed/21493818 Monocyte early outgrowth colony forming units rs6712720 4.00E-06 Genetic and clinical correlates of early-outgrowth colony-forming units. NHGRI|-1
NM_138559 BCL11A 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs10202231 7.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_138559 BCL11A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs243023 1.13E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_138559 BCL11A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs243023 5.95E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_138559 BCL11A 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs243021 3.00E-15 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_138559 BCL11A 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs2540917 1.00E-14 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_138563 KLK15 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs266849 6.00E-10 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_138564 KLK15 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs266849 6.00E-10 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_138568 EXOC3L2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 "Cholesterol, LDL" rs2159324 4.00E-07 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_138568 EXOC3L2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Cholesterol rs2159324 2.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_138570 SLC38A10 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs10445407 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_138574 HDGFL1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 "Cholesterol, HDL" rs10498712 9.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_138574 HDGFL1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2480006 2.43E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_138574 HDGFL1 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs1341239 4.00E-06 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_138609 H2AFY 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs31198 8.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_138609 H2AFY 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs254560 1.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_138609 H2AFY 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs477687 6.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_138610 H2AFY 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs31198 8.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_138610 H2AFY 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs254560 1.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_138610 H2AFY 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs477687 6.00E-06 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_138612 HAS3 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs8047014 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_138620 DDX31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17149424 3.64E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_138621 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_138621 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_138622 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_138622 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_138623 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_138623 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_138624 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_138624 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_138625 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_138625 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_138626 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_138626 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_138627 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_138627 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_138632 TRIOBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs16985637 3.13E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_138634 MSMB 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Prostate-Specific Antigen rs10993994 7.00E-13 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_138634 MSMB 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs10993994 3.00E-08 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_138634 MSMB 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs10993994 5.00E-06 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_138634 MSMB 18264096 http://www.ncbi.nlm.nih.gov/pubmed/18264096 Prostatic Neoplasms rs10993994 7.00E-13 Multiple loci identified in a genome-wide association study of prostate cancer. NHGRI|-1
NM_138634 MSMB 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs10993994 9.00E-29 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_138636 TLR8 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs5979785 6.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_138693 KLF14 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs972283 2.00E-10 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_138694 PKHD1 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Prostatic Neoplasms rs10498792 3.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_138694 PKHD1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs6935568 7.44E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_138697 TAS1R1 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Basophils rs11587438 4.00E-06 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_138700 TRIM40 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2021723 8.69E-15 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_138700 TRIM40 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs757262 7.80E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_138700 TRIM40 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs757259 5.10E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_138700 TRIM40 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs1015465 3.69E-15 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_138700 TRIM40 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9261434 1.75E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_138700 TRIM40 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs10947055 2.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_138704 NDNL2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1471225 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_138709 DAB2IP 20622881 http://www.ncbi.nlm.nih.gov/pubmed/20622881 "Aortic Aneurysm, Abdominal" rs7025486 5.00E-10 Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm. NHGRI|-1
NM_138711 PPARG 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1801282 2.00E-06 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_138711 PPARG 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs1801282 2.00E-06 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_138711 PPARG 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs1801282 2.00E-06 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_138711 PPARG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs9833097 6.72E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_138712 PPARG 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1801282 2.00E-06 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_138712 PPARG 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs1801282 2.00E-06 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_138712 PPARG 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs1801282 2.00E-06 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_138712 PPARG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs9833097 6.72E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_138713 NFAT5 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1364063 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_138714 NFAT5 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1364063 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_138715 MSR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs8181023 8.82E-05 NBL-GWAS version 2 dbGaP|2895
NM_138716 MSR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs8181023 8.82E-05 NBL-GWAS version 2 dbGaP|2895
NM_138717 PPT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3134603 3.36E-116 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_138717 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3096697 2.16E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_138717 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3096697 5.66E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_138717 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130347 1.22E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_138717 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130347 3.62E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_138735 NRXN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10196324 6.42E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_138735 NRXN1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs1356888 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_138735 NRXN1 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Exploratory Behavior rs10176705 9.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_138735 NRXN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs991902 3.48E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_138735 NRXN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2839839 7.09E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_138735 NRXN1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1156742 8.14E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_138737 HEPH 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs5965182 6.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_138766 PAM 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs1502844 1.00E-06 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_138768 MYEOV 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs11228565 7.00E-12 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_138768 MYEOV 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs7931342 2.00E-12 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_138768 MYEOV 18264096 http://www.ncbi.nlm.nih.gov/pubmed/18264096 Prostatic Neoplasms rs10896449 2.00E-09 Multiple loci identified in a genome-wide association study of prostate cancer. NHGRI|-1
NM_138768 MYEOV 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs7130881 8.00E-13 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_138768 MYEOV 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs7130881 9.00E-09 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_138780 SYTL5 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs872690 9.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_138780 SYTL5 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs761913 5.02E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_138794 LYPLAL1 19557161 http://www.ncbi.nlm.nih.gov/pubmed/19557161 Adiposity rs2605100 3.00E-08 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. NHGRI|-1
NM_138794 LYPLAL1 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs4846567 5.00E-33 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_138794 LYPLAL1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1018040 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_138794 LYPLAL1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1018040 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_138801 GALM 21339755 http://www.ncbi.nlm.nih.gov/pubmed/21339755 Serotonin Plasma Membrane Transport Proteins rs6741892 5.00E-06 A non-synonymous polymorphism in galactose mutarotase (GALM) is associated with serotonin transporter binding potential in the human thalamus: results of a genome-wide association study. NHGRI|-1
NM_138810 TAGAP 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1738074 3.00E-15 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_138810 TAGAP 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs1738074 7.00E-08 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_138810 TAGAP 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs212388 2.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_138810 TAGAP 21298027 http://www.ncbi.nlm.nih.gov/pubmed/21298027 Intestinal Diseases rs212388 2.00E-10 "A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease." NHGRI|-1
NM_138810 TAGAP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2016588 1.29E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_138810 TAGAP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2057061 3.47E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_138813 ATP8B3 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs7250872 2.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_138821 PAM 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs1502844 1.00E-06 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_138822 PAM 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs1502844 1.00E-06 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_138937 REG3A 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs13409348 3.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_138937 REG3A 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs399885 5.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_138937 REG3A 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs7570469 6.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_138938 REG3A 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs13409348 3.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_138938 REG3A 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs399885 5.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_138938 REG3A 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs7570469 6.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_138962 MSI2 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs792376 2.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_138969 SDR16C5 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs9650315 4.00E-07 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_138969 SDR16C5 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs7815788 5.00E-06 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_138970 NRXN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs17107542 7.51E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_138970 NRXN3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs918270 5.55E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_138970 NRXN3 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10150332 3.00E-11 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_138970 NRXN3 19557197 http://www.ncbi.nlm.nih.gov/pubmed/19557197 Waist Circumference rs10146997 5.00E-08 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. NHGRI|-1
NM_138970 NRXN3 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs11624704 3.00E-09 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_138994 CNTNAP4 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs13330107 9.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_139003 HFE 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs1799945 3.00E-09 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_139003 HFE 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs1800562 2.00E-32 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_139003 HFE 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs1800562 1.00E-23 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_139003 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 1.00E-46 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139003 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Erythrocyte Indices rs1800562 2.00E-08 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139003 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 3.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139003 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 6.00E-19 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139003 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 6.00E-07 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139003 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs1800562 2.00E-09 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139003 HFE 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1800562 3.00E-20 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_139003 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Hemoglobins rs1800562 5.00E-07 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139003 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Iron rs1800562 4.00E-11 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139003 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 1.00E-10 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139003 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 4.00E-15 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139004 HFE 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs1799945 3.00E-09 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_139004 HFE 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs1800562 2.00E-32 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_139004 HFE 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs1800562 1.00E-23 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_139004 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 1.00E-46 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139004 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Erythrocyte Indices rs1800562 2.00E-08 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139004 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 3.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139004 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 6.00E-19 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139004 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 6.00E-07 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139004 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs1800562 2.00E-09 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139004 HFE 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1800562 3.00E-20 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_139004 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Hemoglobins rs1800562 5.00E-07 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139004 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Iron rs1800562 4.00E-11 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139004 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 1.00E-10 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139004 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 4.00E-15 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139006 HFE 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs1799945 3.00E-09 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_139006 HFE 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs1800562 2.00E-32 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_139006 HFE 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs1800562 1.00E-23 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_139006 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 1.00E-46 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139006 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Erythrocyte Indices rs1800562 2.00E-08 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139006 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 3.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139006 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 6.00E-19 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139006 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 6.00E-07 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139006 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs1800562 2.00E-09 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139006 HFE 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1800562 3.00E-20 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_139006 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Hemoglobins rs1800562 5.00E-07 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139006 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Iron rs1800562 4.00E-11 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139006 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 1.00E-10 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139006 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 4.00E-15 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139007 HFE 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs1799945 3.00E-09 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_139007 HFE 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs1800562 2.00E-32 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_139007 HFE 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs1800562 1.00E-23 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_139007 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 1.00E-46 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139007 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Erythrocyte Indices rs1800562 2.00E-08 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139007 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 3.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139007 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 6.00E-19 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139007 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 6.00E-07 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139007 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs1800562 2.00E-09 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139007 HFE 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1800562 3.00E-20 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_139007 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Hemoglobins rs1800562 5.00E-07 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139007 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Iron rs1800562 4.00E-11 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139007 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 1.00E-10 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139007 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 4.00E-15 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139008 HFE 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs1799945 3.00E-09 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_139008 HFE 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs1800562 2.00E-32 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_139008 HFE 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs1800562 1.00E-23 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_139008 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 1.00E-46 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139008 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Erythrocyte Indices rs1800562 2.00E-08 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139008 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 3.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139008 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 6.00E-19 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139008 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 6.00E-07 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139008 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs1800562 2.00E-09 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139008 HFE 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1800562 3.00E-20 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_139008 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Hemoglobins rs1800562 5.00E-07 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139008 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Iron rs1800562 4.00E-11 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139008 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 1.00E-10 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139008 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 4.00E-15 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139009 HFE 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs1799945 3.00E-09 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_139009 HFE 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs1800562 2.00E-32 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_139009 HFE 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs1800562 1.00E-23 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_139009 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 1.00E-46 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139009 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Erythrocyte Indices rs1800562 2.00E-08 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139009 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 3.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139009 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 6.00E-19 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139009 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 6.00E-07 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139009 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs1800562 2.00E-09 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139009 HFE 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1800562 3.00E-20 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_139009 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Hemoglobins rs1800562 5.00E-07 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139009 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Iron rs1800562 4.00E-11 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139009 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 1.00E-10 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139009 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 4.00E-15 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139010 HFE 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs1799945 3.00E-09 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_139010 HFE 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs1800562 2.00E-32 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_139010 HFE 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs1800562 1.00E-23 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_139010 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 1.00E-46 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139010 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Erythrocyte Indices rs1800562 2.00E-08 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139010 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 3.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139010 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 6.00E-19 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139010 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 6.00E-07 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139010 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs1800562 2.00E-09 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139010 HFE 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1800562 3.00E-20 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_139010 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Hemoglobins rs1800562 5.00E-07 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139010 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Iron rs1800562 4.00E-11 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139010 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 1.00E-10 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139010 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 4.00E-15 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139011 HFE 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs1799945 3.00E-09 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_139011 HFE 21665994 http://www.ncbi.nlm.nih.gov/pubmed/21665994 carbohydrate-deficient transferrin [Supplementary Concept] rs1800562 2.00E-32 Genome-wide association study identifies two loci strongly affecting transferrin glycosylation. NHGRI|-1
NM_139011 HFE 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs1800562 1.00E-23 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_139011 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 1.00E-46 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139011 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Erythrocyte Indices rs1800562 2.00E-08 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139011 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 3.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139011 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs1800562 6.00E-19 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139011 HFE 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs1800562 6.00E-07 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_139011 HFE 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs1800562 2.00E-09 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_139011 HFE 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs1800562 3.00E-20 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_139011 HFE 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Hemoglobins rs1800562 5.00E-07 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_139011 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Iron rs1800562 4.00E-11 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139011 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 1.00E-10 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139011 HFE 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs1800562 4.00E-15 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139015 SPPL3 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 C-Reactive Protein rs1039302 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_139017 IL31RA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs162096 3.33E-05 NBL-GWAS version 2 dbGaP|2895
NM_139018 CD300LF 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs10512597 8.00E-11 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_139025 ADAMTS13 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs4962153 8.00E-21 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_139025 ADAMTS13 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs4962153 8.05E-14 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_139026 ADAMTS13 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs4962153 8.00E-21 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_139026 ADAMTS13 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs4962153 8.05E-14 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_139027 ADAMTS13 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs4962153 8.00E-21 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_139027 ADAMTS13 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs4962153 8.05E-14 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_139053 EPS8L3 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs10494112 7.00E-35 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_139053 EPS8L3 20436471 http://www.ncbi.nlm.nih.gov/pubmed/20436471 Osteitis Deformans rs484959 5.00E-24 "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone." NHGRI|-1
NM_139053 EPS8L3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs525566 5.88E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_139056 ADAMTS16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4323203 1.63E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_139056 ADAMTS16 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs13187879 1.23E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_139056 ADAMTS16 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7723605 5.65E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_139056 ADAMTS16 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2964459 5.40E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_139056 ADAMTS16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs13359418 9.17E-05 NBL-GWAS version 2 dbGaP|2895
NM_139056 ADAMTS16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs16872251 9.48E-05 NBL-GWAS version 2 dbGaP|2895
NM_139056 ADAMTS16 21107343 http://www.ncbi.nlm.nih.gov/pubmed/21107343 Myocardial Infarction rs11748327 5.00E-13 SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population. NHGRI|-1
NM_139056 ADAMTS16 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs7727102 1.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_139057 ADAMTS17 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12148118 1.63E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_139057 ADAMTS17 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs4533267 3.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_139058 ARX 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs5944185 7.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_139075 TPCN2 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs3750965 3.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_139075 TPCN2 18488028 http://www.ncbi.nlm.nih.gov/pubmed/18488028 Hair Color rs35264875 4.00E-30 Two newly identified genetic determinants of pigmentation in Europeans. NHGRI|-1
NM_139075 TPCN2 19767754 http://www.ncbi.nlm.nih.gov/pubmed/19767754 Prostatic Neoplasms rs11228565 7.00E-12 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility. NHGRI|-1
NM_139075 TPCN2 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs7931342 2.00E-12 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_139075 TPCN2 18264096 http://www.ncbi.nlm.nih.gov/pubmed/18264096 Prostatic Neoplasms rs10896449 2.00E-09 Multiple loci identified in a genome-wide association study of prostate cancer. NHGRI|-1
NM_139075 TPCN2 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs7130881 8.00E-13 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_139075 TPCN2 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs7130881 9.00E-09 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_139118 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs651905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_139118 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs602905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_139119 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs651905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_139119 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs602905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_139121 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs651905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_139121 YY1AP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs602905 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_139155 ADAMTS14 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs7092269 5.29E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_139155 ADAMTS14 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs1816002 8.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_139158 CDK15 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17385675 3.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_139166 ABRA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4734938 8.67E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_139167 SGCZ 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7824519 6.00E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_139167 SGCZ 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs1903595 5.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_139167 SGCZ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs10503501 8.36E-04 Genome-wide association between genotype and incident myocardial infarction in African-American participants dbGaP|2883
NM_139167 SGCZ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6985300 4.38E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_139167 SGCZ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1390052 8.02E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_139167 SGCZ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1390053 7.02E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_139167 SGCZ 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11785331 2.85E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_139177 SLC39A11 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs8066857 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_139201 GIT2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs2292354 7.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_139201 GIT2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11068997 7.24E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_139243 ADAD1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs17388568 9.00E-07 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_139243 ADAD1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs17388568 3.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_139244 STXBP5 20231535 http://www.ncbi.nlm.nih.gov/pubmed/20231535 Blood Coagulation Factors rs9390459 1.00E-22 "Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium." NHGRI|-1
NM_139244 STXBP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs9390459 2.10E-04 Genome-wide association between genotype and incident heart failure in African-American participants dbGaP|2885
NM_139244 STXBP5 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs9373523 1.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_139273 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs729662 8.52E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_139273 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7481584 9.54E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_139273 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_139273 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 4.55E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_139273 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 7.54E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_139273 CARS 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs739401 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_139273 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs438384 1.07E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_139273 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 2.60E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_139273 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 3.06E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_139273 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 9.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_139273 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs369461 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_139273 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs369461 7.87E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_139276 STAT3 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs744166 7.00E-12 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_139276 STAT3 20159113 http://www.ncbi.nlm.nih.gov/pubmed/20159113 Multiple Sclerosis rs744166 3.00E-10 Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. NHGRI|-1
NM_139279 MCFD2 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs76351433 2.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_139280 ORMDL3 21150878 http://www.ncbi.nlm.nih.gov/pubmed/21150878 Asthma rs6503525 5.00E-07 "Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia." NHGRI|-1
NM_139280 ORMDL3 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Leukocyte Count rs17609240 9.00E-09 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_139281 WDR36 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Eosinophils rs2416257 1.00E-06 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_139316 AMPH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6967370 5.10E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_139318 KCNH5 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs973968 3.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_139318 KCNH5 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1514928 3.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_139343 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs12989701 3.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139343 BIN1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs7561528 4.00E-14 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_139343 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs744373 1.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139343 BIN1 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs744373 2.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_139343 BIN1 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs744373 3.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_139343 BIN1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs13418717 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_139344 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs12989701 3.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139344 BIN1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs7561528 4.00E-14 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_139344 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs744373 1.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139344 BIN1 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs744373 2.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_139344 BIN1 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs744373 3.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_139344 BIN1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs13418717 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_139345 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs12989701 3.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139345 BIN1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs7561528 4.00E-14 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_139345 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs744373 1.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139345 BIN1 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs744373 2.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_139345 BIN1 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs744373 3.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_139345 BIN1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs13418717 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_139346 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs12989701 3.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139346 BIN1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs7561528 4.00E-14 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_139346 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs744373 1.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139346 BIN1 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs744373 2.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_139346 BIN1 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs744373 3.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_139346 BIN1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs13418717 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_139347 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs12989701 3.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139347 BIN1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs7561528 4.00E-14 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_139347 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs744373 1.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139347 BIN1 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs744373 2.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_139347 BIN1 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs744373 3.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_139347 BIN1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs13418717 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_139348 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs12989701 3.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139348 BIN1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs7561528 4.00E-14 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_139348 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs744373 1.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139348 BIN1 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs744373 2.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_139348 BIN1 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs744373 3.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_139348 BIN1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs13418717 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_139349 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs12989701 3.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139349 BIN1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs7561528 4.00E-14 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_139349 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs744373 1.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139349 BIN1 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs744373 2.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_139349 BIN1 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs744373 3.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_139349 BIN1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs13418717 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_139350 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs12989701 3.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139350 BIN1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs7561528 4.00E-14 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_139350 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs744373 1.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139350 BIN1 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs744373 2.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_139350 BIN1 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs744373 3.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_139350 BIN1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs13418717 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_139351 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs12989701 3.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139351 BIN1 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs7561528 4.00E-14 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_139351 BIN1 21390209 http://www.ncbi.nlm.nih.gov/pubmed/21390209 Alzheimer Disease rs744373 1.00E-10 Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. NHGRI|-1
NM_139351 BIN1 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs744373 2.00E-09 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_139351 BIN1 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs744373 3.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_139351 BIN1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs13418717 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_144492 CLDN14 19561606 http://www.ncbi.nlm.nih.gov/pubmed/19561606 Kidney Calculi rs219780 4.00E-12 Sequence variants in the CLDN14 gene associate with kidney stones and bone mineral density. NHGRI|-1
NM_144585 SLC22A12 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs505802 2.00E-09 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7893461 1.65E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7893461 1.92E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1028631 5.23E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs911774 8.90E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7907952 1.51E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3817285 4.13E-09 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3817285 5.21E-10 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11200559 8.33E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7091160 1.81E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6585818 1.92E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11598094 2.21E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11598094 5.64E-07 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7080960 4.24E-11 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7080960 5.76E-12 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11200583 5.76E-16 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11200583 8.67E-16 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751889 1.73E-14 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_144587 BTBD16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4751889 2.26E-15 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_144591 C10orf32 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs3824754 3.92E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_144591 C10orf32 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11191425 3.96E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_144620 LRRC39 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6677080 1.44E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_144620 LRRC39 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11166407 2.01E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_144625 WDR64 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs12569163 2.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_144632 TMEM182 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs6735786 2.00E-06 New sequence variants associated with bone mineral density. NHGRI|-1
NM_144633 KCNH8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs997384 9.29E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_144633 KCNH8 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs2053506 4.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_144633 KCNH8 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs6792314 8.60E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144633 KCNH8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11914608 1.42E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_144633 KCNH8 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs13073817 7.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_144633 KCNH8 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs6809854 1.00E-07 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_144634 LYZL4 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs2286720 1.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_144647 CAPSL 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs1445898 8.00E-06 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_144647 CAPSL 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs860413 1.00E-11 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_144647 CAPSL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2194225 6.57E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_144651 PXDNL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6473406 3.88E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_144651 PXDNL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6473431 9.09E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_144651 PXDNL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7013653 3.21E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_144651 PXDNL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7016107 6.32E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_144651 PXDNL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10102886 8.33E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_144651 PXDNL 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs7821565 8.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_144664 FAM76B 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs1939875 3.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_144665 SESN3 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs1939875 3.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_144668 WDR66 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs7961894 3.00E-44 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_144668 WDR66 19110211 http://www.ncbi.nlm.nih.gov/pubmed/19110211 Platelet Count rs7961894 7.00E-48 A genome-wide association study identifies three loci associated with mean platelet volume. NHGRI|-1
NM_144668 WDR66 21572414 http://www.ncbi.nlm.nih.gov/pubmed/21572414 Metabolism rs830124 1.00E-46 A genome-wide association study of metabolic traits in human urine. NHGRI|-1
NM_144672 OTOA 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs8050407 2.20E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_144674 TEKT5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2719726 5.25E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_144674 TEKT5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2251984 7.45E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_144674 TEKT5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2251985 5.09E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_144674 TEKT5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4780986 9.42E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_144674 TEKT5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4780959 8.18E-05 NBL-GWAS version 2 dbGaP|2895
NM_144675 GSG1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs8051871 1.14E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_144677 MGAT5B 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9916886 4.52E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_144681 CCDC42 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1971773 5.48E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_144681 CCDC42 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6503137 8.24E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_144696 C1orf125 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs12047808 6.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2064689 4.96E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs10489630 7.60E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1004819 1.50E-09 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144701 IL23R 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs11805303 6.00E-12 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_144701 IL23R 17435756 http://www.ncbi.nlm.nih.gov/pubmed/17435756 Crohn Disease rs7517847 3.00E-12 Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. NHGRI|-1
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs7517847 2.99E-13 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs7517847 4.00E-13 A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. NHGRI|-1
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs10489629 6.79E-11 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144701 IL23R 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs2201841 1.00E-13 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2201841 3.57E-10 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144701 IL23R 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs2201841 3.00E-08 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NM_144701 IL23R 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs11465804 1.00E-06 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_144701 IL23R 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs11465804 7.00E-63 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11465804 3.74E-10 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144701 IL23R 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs11209026 1.00E-08 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_144701 IL23R 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs11209026 3.00E-10 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_144701 IL23R 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs11209026 5.00E-28 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_144701 IL23R 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs11209026 1.00E-64 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_144701 IL23R 17447842 http://www.ncbi.nlm.nih.gov/pubmed/17447842 Crohn Disease rs11209026 2.00E-18 Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4. NHGRI|-1
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11209026 4.59E-11 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11209026 4.00E-11 A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. NHGRI|-1
NM_144701 IL23R 18758464 http://www.ncbi.nlm.nih.gov/pubmed/18758464 Inflammatory Bowel Diseases rs11209026 7.00E-11 Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. NHGRI|-1
NM_144701 IL23R 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs11209026 7.00E-07 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_144701 IL23R 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs11209026 2.00E-17 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_144701 IL23R 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs11209026 9.00E-14 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1343151 1.63E-11 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144701 IL23R 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 "Colitis, Ulcerative" rs10889677 1.00E-08 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs10889677 9.04E-11 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs7539328 1.10E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11209032 8.65E-10 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144701 IL23R 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1495966 6.09E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_144701 IL23R 20622879 http://www.ncbi.nlm.nih.gov/pubmed/20622879 Behcet Syndrome rs1495965 2.00E-11 Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behtet's disease susceptibility loci. NHGRI|-1
NM_144701 IL23R 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1495965 6.99E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1495965 1.51E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144701 IL23R 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs924080 5.35E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_144701 IL23R 20622878 http://www.ncbi.nlm.nih.gov/pubmed/20622878 Behcet Syndrome rs924080 7.00E-09 "Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behtet's disease." NHGRI|-1
NM_144701 IL23R 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs924080 2.57E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_144709 PUS10 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs13003464 4.00E-13 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_144709 PUS10 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs13003464 7.00E-09 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_144709 PUS10 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs7608910 2.00E-14 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_144709 PUS10 21298027 http://www.ncbi.nlm.nih.gov/pubmed/21298027 Intestinal Diseases rs10188217 1.00E-11 "A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease." NHGRI|-1
NM_144709 PUS10 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs10181042 7.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_144713 FAM82A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1374196 7.26E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_144713 FAM82A1 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs6741148 4.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_144713 FAM82A1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs4670766 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_144713 FAM82A1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs17511102 2.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_144713 FAM82A1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs604381 8.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_144713 FAM82A1 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs4670779 4.00E-06 New sequence variants associated with bone mineral density. NHGRI|-1
NM_144717 IL20RB 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Sphingomyelins rs1382269 5.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_144719 CCDC13 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs339676 5.84E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_144722 SPEF2 21244703 http://www.ncbi.nlm.nih.gov/pubmed/21244703 Multiple Sclerosis rs931555 4.00E-07 Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data. NHGRI|-1
NM_144722 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286411 2.12E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_144722 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 5.38E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_144722 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 6.67E-07 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_144722 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs169587 1.61E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_144722 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1605683 1.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_144722 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286388 1.39E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_144722 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 1.29E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_144722 SPEF2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 3.17E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_144726 RNF145 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs1473247 3.00E-07 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_144727 CRYGN 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs13232179 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_144728 DUSP10 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10495179 8.26E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_144728 DUSP10 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs11118864 2.88E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_144728 DUSP10 20972440 http://www.ncbi.nlm.nih.gov/pubmed/20972440 Colorectal Neoplasms rs6691170 1.00E-09 "Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33." NHGRI|-1
NM_144728 DUSP10 20972440 http://www.ncbi.nlm.nih.gov/pubmed/20972440 Colorectal Neoplasms rs6687758 2.00E-09 "Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33." NHGRI|-1
NM_144728 DUSP10 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs6687758 6.00E-08 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_144728 DUSP10 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs873549 6.00E-23 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_144728 DUSP10 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs12733856 3.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_144728 DUSP10 20971583 http://www.ncbi.nlm.nih.gov/pubmed/20971583 Dupuytren Contracture rs12032381 6.00E-06 Genome-wide association scan of Dupuytren's disease. NHGRI|-1
NM_144729 DUSP10 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10495179 8.26E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_144729 DUSP10 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs11118864 2.88E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_144729 DUSP10 20972440 http://www.ncbi.nlm.nih.gov/pubmed/20972440 Colorectal Neoplasms rs6691170 1.00E-09 "Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33." NHGRI|-1
NM_144729 DUSP10 20972440 http://www.ncbi.nlm.nih.gov/pubmed/20972440 Colorectal Neoplasms rs6687758 2.00E-09 "Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33." NHGRI|-1
NM_144729 DUSP10 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs6687758 6.00E-08 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_144729 DUSP10 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs873549 6.00E-23 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_144729 DUSP10 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs12733856 3.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_144729 DUSP10 20971583 http://www.ncbi.nlm.nih.gov/pubmed/20971583 Dupuytren Contracture rs12032381 6.00E-06 Genome-wide association scan of Dupuytren's disease. NHGRI|-1
NM_144765 MPZL2 19207018 http://www.ncbi.nlm.nih.gov/pubmed/19207018 Pain Measurement rs17122021 7.00E-07 Genome-wide association study of acute post-surgical pain in humans. NHGRI|-1
NM_144767 AKAP13 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs11858860 8.88E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_144767 AKAP13 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs7171364 8.87E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_144767 AKAP13 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs383872 2.12E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_144767 AKAP13 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs338538 2.10E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_144767 AKAP13 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs6496932 1.00E-08 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NM_144778 MBNL2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs9516905 5.94E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_144778 MBNL2 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs9556711 2.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_144778 MBNL2 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs9556711 8.00E-07 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_144779 FXYD5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2285515 7.66E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_144949 SOCS5 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs76351433 2.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_144963 FAM91A1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs10481151 4.00E-07 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_144963 FAM91A1 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs10088262 4.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_144966 FREM1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs10961780 2.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_144974 CCDC122 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs3088362 1.37E-09 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_144977 DENND1B 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs1998598 9.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_144979 RBM46 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs7684755 5.20E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_144980 C6orf118 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 "Arthritis, Rheumatoid" rs10945919 3.00E-07 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_144980 C6orf118 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9356147 3.45E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_144980 C6orf118 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs10428875 8.47E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_144980 C6orf118 20516156 http://www.ncbi.nlm.nih.gov/pubmed/20516156 "Depressive Disorder, Major" rs4709845 9.00E-06 Genome-wide association study of major recurrent depression in the U.K. population. NHGRI|-1
NM_144980 C6orf118 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2201806 1.23E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_144980 C6orf118 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6455970 2.15E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_144980 C6orf118 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9459317 6.76E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_144980 C6orf118 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1764053 5.00E-16 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_144980 C6orf118 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1923608 7.61E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_144980 C6orf118 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs16897566 2.75E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_144984 C10orf72 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs2244967 5.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_144989 DNAH14 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2662928 8.79E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_144989 DNAH14 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs1892121 6.78E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_144991 C21orf29 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12627324 6.41E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_144991 C21orf29 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9637184 2.94E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_144992 VWA3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7603439 2.00E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_144992 VWA3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6715989 1.69E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_144992 VWA3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7571001 1.95E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_144993 TET3 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs6546886 3.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_145000 RANBP3L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4354072 1.61E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_145005 C9orf72 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs774359 3.00E-06 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_145005 C9orf72 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs12555345 5.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_145005 C9orf72 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs7029145 9.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_145005 C9orf72 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs10812610 3.47E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_145005 C9orf72 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs10812610 5.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_145005 C9orf72 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs2814707 7.00E-09 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_145005 C9orf72 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs3849942 1.00E-08 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_145005 C9orf72 20801718 http://www.ncbi.nlm.nih.gov/pubmed/20801718 Amyotrophic Lateral Sclerosis rs3849942 9.00E-11 Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. NHGRI|-1
NM_145007 NLRP11 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs299175 4.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_145007 NLRP11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1423071 4.65E-06 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_145010 ENKUR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2307047 6.17E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_145012 CCNY 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs12261843 7.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_145012 CCNY 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12261843 4.05E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_145021 8-Mar 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs2279434 4.00E-12 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_145021 8-Mar 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs11239550 1.00E-10 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_145025 AKD1 19684573 http://www.ncbi.nlm.nih.gov/pubmed/19684573 Hepatitis C rs9400317 7.00E-06 Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance. NHGRI|-1
NM_145027 KIF6 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Attention Deficit Disorder with Hyperactivity rs4714261 2.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_145036 CCDC46 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs8074751 1.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_145036 CCDC46 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Weight rs7209395 3.00E-06 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_145036 CCDC46 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs757558 6.42E-06 NBL-GWAS version 1 dbGaP|2845
NM_145043 NEIL2 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs6601606 1.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_145047 OSCP1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs6702784 4.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_145049 UBLCP1 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs2082412 2.00E-28 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NM_145060 SKA1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2119547 3.65E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_145060 SKA1 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 "Leukemia, Lymphocytic, Chronic, B-Cell" rs1036935 2.00E-06 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_145065 PELI3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1791682 1.08E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_145102 ZKSCAN5 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs11761528 3.00E-36 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_145112 MAX 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4466998 5.00E-08 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_145112 MAX 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Waist Circumference rs7158173 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_145113 MAX 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4466998 5.00E-08 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_145113 MAX 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Waist Circumference rs7158173 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_145114 MAX 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4466998 5.00E-08 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_145114 MAX 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Waist Circumference rs7158173 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_145115 ZNF498 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Anthropometry rs7792939 5.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_145115 ZNF498 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weight rs7792939 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_145115 ZNF498 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weights and Measures rs7792939 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_145116 MAX 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4466998 5.00E-08 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_145116 MAX 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Waist Circumference rs7158173 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_145117 NAV2 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs874426 4.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_145160 MAP2K5 17637780 http://www.ncbi.nlm.nih.gov/pubmed/17637780 Restless Legs Syndrome rs12593813 1.00E-15 Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. NHGRI|-1
NM_145160 MAP2K5 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2241423 1.00E-18 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_145178 ATOH7 21307088 http://www.ncbi.nlm.nih.gov/pubmed/21307088 Optic Disk rs7916697 2.00E-15 "Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area." NHGRI|-1
NM_145178 ATOH7 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1900004 2.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_145178 ATOH7 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1900004 3.00E-35 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_145178 ATOH7 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs3858145 2.00E-07 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_145178 ATOH7 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Optic Disk rs3858145 3.00E-10 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_145178 ATOH7 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Optic Disk rs12571093 2.00E-10 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_145200 CABP4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs11601325 5.85E-06 NBL-GWAS version 1 dbGaP|2845
NM_145201 NAPRT1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs2290416 9.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_145206 VTI1A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs7342028 5.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_145231 C14orf143 21105107 http://www.ncbi.nlm.nih.gov/pubmed/21105107 "Carcinoma, Hepatocellular" rs12100561 4.00E-06 Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma. NHGRI|-1
NM_145231 C14orf143 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4900016 3.53E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_145234 CHRDL1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs5943057 9.00E-07 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_145235 FANK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs17153882 2.91E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_145243 OMA1 21221998 http://www.ncbi.nlm.nih.gov/pubmed/21221998 Mucocutaneous Lymph Node Syndrome rs527409 1.00E-06 A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease. NHGRI|-1
NM_145245 EVI5L 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs558718 4.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_145248 C13orf28 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs7992158 1.08E-04 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_145249 IFI27L1 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weight rs7157940 3.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_145259 ACVR1C 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2444769 9.19E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_145260 OSR1 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognition rs1876040 6.00E-08 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_145263 SPATA18 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Triglycerides rs346923 2.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_145267 C6orf57 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs1048886 3.00E-08 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_145285 NKX2-3 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs11190140 1.00E-08 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_145285 NKX2-3 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs11190140 3.00E-16 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_145285 NKX2-3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs4409764 2.00E-20 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_145285 NKX2-3 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs10883365 4.00E-10 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_145285 NKX2-3 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs10883365 6.00E-08 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_145285 NKX2-3 20228798 http://www.ncbi.nlm.nih.gov/pubmed/20228798 "Colitis, Ulcerative" rs6584283 2.00E-06 Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). NHGRI|-1
NM_145285 NKX2-3 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs6584283 2.00E-07 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_145285 NKX2-3 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6584283 8.00E-21 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_145286 STOML3 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs9315632 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_145290 GPR125 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs9992275 1.05E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_145290 GPR125 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2323262 4.31E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_145305 SLC25A43 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs5910578 1.00E-07 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_145313 RASGEF1A 20598377 http://www.ncbi.nlm.nih.gov/pubmed/20598377 Multiple Sclerosis rs2503875 2.00E-07 Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. NHGRI|-1
NM_145316 TMEM217 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs262929 1.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_145326 ZNF493 19207018 http://www.ncbi.nlm.nih.gov/pubmed/19207018 Pain Measurement rs2562456 2.00E-10 Genome-wide association study of acute post-surgical pain in humans. NHGRI|-1
NM_145331 MAP3K7 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs713155 5.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_145331 MAP3K7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1145724 4.14E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_145331 MAP3K7 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs806276 3.00E-07 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_145332 MAP3K7 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs713155 5.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_145332 MAP3K7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1145724 4.14E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_145332 MAP3K7 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs806276 3.00E-07 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_145333 MAP3K7 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs713155 5.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_145333 MAP3K7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs1145724 4.14E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_145333 MAP3K7 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs806276 3.00E-07 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_145343 APOL1 20668430 http://www.ncbi.nlm.nih.gov/pubmed/20668430 "Glomerulosclerosis, Focal Segmental" rs2239785 5.00E-13 A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. NHGRI|-1
NM_145637 APOL2 20532800 http://www.ncbi.nlm.nih.gov/pubmed/20532800 "Kidney Failure, Chronic" rs4821469 2.00E-19 Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA. NHGRI|-1
NM_145638 OSBPL5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4758533 4.82E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_145648 SLC15A4 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs1385374 2.00E-11 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_145657 GSX1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs9512900 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_145659 IL27 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs4788084 3.00E-13 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_145660 APOL4 20532800 http://www.ncbi.nlm.nih.gov/pubmed/20532800 "Kidney Failure, Chronic" rs4821469 2.00E-19 Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA. NHGRI|-1
NM_145690 YWHAZ 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs3491 1.79E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_145690 YWHAZ 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs931812 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_145693 LPIN1 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs17605562 9.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_145695 DGKB 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs6971925 3.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_145699 APOBEC3A 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs1014971 8.00E-12 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_145714 ATXN2L 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory Bowel Diseases rs8049439 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_145725 TRAF3 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs10133111 5.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_145726 TRAF3 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs10133111 5.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_145731 SYNGR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1569499 5.54E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_145731 SYNGR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4821888 1.14E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_145735 ARHGEF7 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs4773330 8.00E-06 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_145738 SYNGR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1569499 5.54E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_145738 SYNGR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4821888 1.14E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_145759 TRAF5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3738200 4.83E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_145759 TRAF5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17189000 5.44E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_145810 CDCA7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2358259 1.39E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_145810 CDCA7 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Mass Index rs7590983 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_145810 CDCA7 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs7581219 8.57E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_145811 CACNG5 21057379 http://www.ncbi.nlm.nih.gov/pubmed/21057379 Mental Disorders rs17645023 6.00E-07 Case-case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes. NHGRI|-1
NM_145862 CHEK2 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic Disk rs1547014 1.00E-08 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_145862 CHEK2 20729852 http://www.ncbi.nlm.nih.gov/pubmed/20729852 Stomach Neoplasms rs738722 1.00E-08 A shared susceptibility locus in PLCE1 at 10q23 for gastric adenocarcinoma and esophageal squamous cell carcinoma. NHGRI|-1
NM_145863 ASB3 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Hemoglobins rs1160297 1.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_145863 ASB3 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Hemoglobins rs2357013 6.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_145891 RBFOX1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs6500744 3.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_145891 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13336322 9.10E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_145891 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7188257 7.46E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_145891 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4786850 3.70E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_145891 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17822719 2.54E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_145891 RBFOX1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit Disorder with Hyperactivity rs12921846 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_145891 RBFOX1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1551960 4.67E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_145891 RBFOX1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs899305 6.31E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_145891 RBFOX1 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Nonalcoholic Fatty Liver Disease rs9302841 2.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_145891 RBFOX1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs4787008 6.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_145891 RBFOX1 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Phosphatidylcholines rs9924951 5.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_145892 RBFOX1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs6500744 3.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_145892 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13336322 9.10E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_145892 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7188257 7.46E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_145892 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4786850 3.70E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_145892 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17822719 2.54E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_145892 RBFOX1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit Disorder with Hyperactivity rs12921846 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_145892 RBFOX1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1551960 4.67E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_145892 RBFOX1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs899305 6.31E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_145892 RBFOX1 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Nonalcoholic Fatty Liver Disease rs9302841 2.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_145892 RBFOX1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs4787008 6.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_145892 RBFOX1 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Phosphatidylcholines rs9924951 5.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_145893 RBFOX1 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs6500744 3.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_145893 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13336322 9.10E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_145893 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7188257 7.46E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_145893 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4786850 3.70E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_145893 RBFOX1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17822719 2.54E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_145893 RBFOX1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit Disorder with Hyperactivity rs12921846 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_145893 RBFOX1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1551960 4.67E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_145893 RBFOX1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs899305 6.31E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_145893 RBFOX1 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Nonalcoholic Fatty Liver Disease rs9302841 2.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_145893 RBFOX1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs4787008 6.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_145893 RBFOX1 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Phosphatidylcholines rs9924951 5.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_145899 HMGA1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1776897 1.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_145899 HMGA1 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs1776897 7.00E-06 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_145899 HMGA1 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs1776897 8.00E-11 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_145901 HMGA1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1776897 1.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_145901 HMGA1 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs1776897 7.00E-06 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_145901 HMGA1 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs1776897 8.00E-11 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_145902 HMGA1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1776897 1.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_145902 HMGA1 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs1776897 7.00E-06 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_145902 HMGA1 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs1776897 8.00E-11 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_145903 HMGA1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1776897 1.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_145903 HMGA1 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs1776897 7.00E-06 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_145903 HMGA1 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs1776897 8.00E-11 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_145905 HMGA1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1776897 1.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_145905 HMGA1 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs1776897 7.00E-06 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_145905 HMGA1 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs1776897 8.00E-11 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_145909 ZNF323 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs853679 2.52E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_145909 ZNF323 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs853676 5.22E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_145909 ZNF323 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs853676 6.14E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_147129 ALS2CL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs7633016 3.19E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_147129 ALS2CL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4076927 2.53E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_147130 NCR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844480 4.62E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_147130 NCR3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs2857595 1.40E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_147130 NCR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2857595 6.48E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_147130 NCR3 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs2844479 2.00E-08 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_147133 NFX1 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs12336160 1.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_147134 NFX1 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs12336160 1.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_147150 AKAP2 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs7032940 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_147152 ITSN2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2543662 5.11E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_147152 ITSN2 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs6707600 3.00E-06 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_147156 SGMS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs3011777 4.16E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_147163 PSMG2 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs2542151 2.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_147163 PSMG2 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs2542151 3.00E-08 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_147163 PSMG2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2542151 5.00E-17 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_147163 PSMG2 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs2542151 1.00E-14 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_147163 PSMG2 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs2542151 9.00E-08 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_147175 HS6ST2 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs17324272 2.00E-07 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_147180 PPP3R2 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs10989661 6.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_147180 PPP3R2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs320209 4.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_147181 KCNIP4 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4697177 6.80E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_147181 KCNIP4 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs6825103 2.13E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_147181 KCNIP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs876477 5.40E-06 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_147181 KCNIP4 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs358592 3.00E-06 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_147181 KCNIP4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4697227 1.84E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_147182 KCNIP4 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4697177 6.80E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_147182 KCNIP4 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs6825103 2.13E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_147182 KCNIP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs876477 5.40E-06 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_147182 KCNIP4 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs358592 3.00E-06 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_147182 KCNIP4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4697227 1.84E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_147183 KCNIP4 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4697177 6.80E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_147183 KCNIP4 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs6825103 2.13E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_147183 KCNIP4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs876477 5.40E-06 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_147183 KCNIP4 20877300 http://www.ncbi.nlm.nih.gov/pubmed/20877300 Suicidal Ideation rs358592 3.00E-06 Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. NHGRI|-1
NM_147183 KCNIP4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4697227 1.84E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_147189 FAM110B 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs954295 4.00E-09 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_147189 FAM110B 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1436013 1.00E-10 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_147189 FAM110B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1992045 7.75E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_147189 FAM110B 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs1992045 2.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_147193 GLIS1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs6588480 8.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_147223 NCOA1 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs2165738 4.00E-06 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_147233 NCOA1 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs2165738 4.00E-06 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_147686 TRAF3IP2 20953186 http://www.ncbi.nlm.nih.gov/pubmed/20953186 "Arthritis, Psoriatic" rs33980500 1.00E-20 Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. NHGRI|-1
NM_147686 TRAF3IP2 20953188 http://www.ncbi.nlm.nih.gov/pubmed/20953188 Psoriasis rs33980500 1.00E-16 Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. NHGRI|-1
NM_148170 CTSC 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17754282 4.30E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_148172 PEMT 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs12936587 4.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_148173 PEMT 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs12936587 4.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_148414 ATXN2L 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory Bowel Diseases rs8049439 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_148415 ATXN2L 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory Bowel Diseases rs8049439 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_148416 ATXN2L 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory Bowel Diseases rs8049439 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_148674 SMC1B 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17639579 6.85E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_148893 SVIP 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs712022 6.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_148893 SVIP 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10833905 7.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_148919 PSMB8 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 "Glomerulonephritis, IGA" rs9357155 2.00E-12 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_148919 PSMB8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2071540 1.26E-69 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_148923 CYB5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10514115 6.18E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_148957 TNFRSF19 20512145 http://www.ncbi.nlm.nih.gov/pubmed/20512145 Nasopharyngeal Neoplasms rs9510787 2.00E-09 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. NHGRI|-1
NM_148957 TNFRSF19 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs753955 2.00E-12 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_148957 TNFRSF19 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9507108 2.60E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_148957 TNFRSF19 20512145 http://www.ncbi.nlm.nih.gov/pubmed/20512145 Nasopharyngeal Neoplasms rs1572072 1.00E-08 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. NHGRI|-1
NM_148959 HUS1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1883628 5.86E-05 NBL-GWAS version 2 dbGaP|2895
NM_148961 OTOS 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs1574192 4.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_148962 OXER1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs930421 6.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_148962 OXER1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs6719977 2.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_148963 GPRC6A 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs6901250 5.00E-08 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_148975 MS4A4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs1026250 1.20E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_148975 MS4A4A 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs1562990 4.00E-11 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_148975 MS4A4A 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs4938933 8.00E-12 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_148977 PANK1 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Insulin rs11185790 3.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_148977 PANK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Insulin rs11185790 9.73E-05 Genomewide association analysis of insulin (INS) in a birth cohort from a founder population dbGaP|2901
NM_148978 PANK1 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Insulin rs11185790 3.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_148978 PANK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Insulin rs11185790 9.73E-05 Genomewide association analysis of insulin (INS) in a birth cohort from a founder population dbGaP|2901
NM_152133 TAGAP 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1738074 3.00E-15 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_152133 TAGAP 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs1738074 7.00E-08 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_152133 TAGAP 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs212388 2.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_152133 TAGAP 21298027 http://www.ncbi.nlm.nih.gov/pubmed/21298027 Intestinal Diseases rs212388 2.00E-10 "A meta-analysis of genome-wide association scans identifies IL18RAP, PTPN2, TAGAP, and PUS10 as shared risk loci for Crohn's disease and celiac disease." NHGRI|-1
NM_152133 TAGAP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2016588 1.29E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_152133 TAGAP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2057061 3.47E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_152226 PPEF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs239748 1.17E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_152230 IPMK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs7899961 5.32E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_152230 IPMK 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs1819658 9.00E-17 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_152232 TAS1R2 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs12063142 5.00E-07 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_152238 SNX7 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1351563 7.27E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_152243 CDC42EP1 21307088 http://www.ncbi.nlm.nih.gov/pubmed/21307088 Optic Disk rs9607469 3.00E-12 "Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area." NHGRI|-1
NM_152245 CPT1B 18820697 http://www.ncbi.nlm.nih.gov/pubmed/18820697 Narcolepsy rs5770917 6.00E-08 Variant between CPT1B and CHKB associated with susceptibility to narcolepsy. NHGRI|-1
NM_152246 CPT1B 18820697 http://www.ncbi.nlm.nih.gov/pubmed/18820697 Narcolepsy rs5770917 6.00E-08 Variant between CPT1B and CHKB associated with susceptibility to narcolepsy. NHGRI|-1
NM_152271 LONRF1 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Survival rs4831837 5.00E-07 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_152291 MUC7 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs1109501 5.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_152308 C16orf75 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs12928822 3.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_152315 FAM55A 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs678170 5.00E-14 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_152324 C13orf16 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2479967 3.11E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_152324 C13orf16 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs9555810 6.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_152324 C13orf16 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs7333181 3.00E-08 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_152330 FRMD6 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs7140150 5.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_152330 FRMD6 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs7153703 3.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_152330 FRMD6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17123958 1.04E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_152332 TC2N 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs17127600 2.74E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_152336 AGBL1 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs16977195 2.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_152336 AGBL1 21448238 http://www.ncbi.nlm.nih.gov/pubmed/21448238 Migraine without Aura rs11636768 5.00E-07 Meta-analysis of genome-wide association for migraine in six population-based European cohorts. NHGRI|-1
NM_152336 AGBL1 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Aging rs7176093 7.00E-06 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_152341 PAQR4 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs886427 6.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_152348 WDR81 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs12150338 7.00E-07 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_152354 ZFP112 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2609881 5.38E-07 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_152360 ZNF573 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs16975963 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_152363 ANKLE1 20852633 http://www.ncbi.nlm.nih.gov/pubmed/20852633 Ovarian Neoplasms rs2363956 1.00E-07 Common variants at 19p13 are associated with susceptibility to ovarian cancer. NHGRI|-1
NM_152367 C1orf161 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7552721 5.96E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_152369 SLC44A3 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs12029080 6.00E-52 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_152371 C1orf93 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs734999 3.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_152374 C1orf216 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6688464 6.00E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_152375 KLHDC7A 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs3007729 5.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_152377 C1orf87 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs2989476 3.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_152377 C1orf87 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs472913 2.00E-07 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_152380 TBX15 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs984222 9.00E-25 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_152380 TBX15 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Body Height rs17038182 5.00E-07 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_152380 TBX15 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs12735613 4.00E-11 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_152381 XIRP2 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs13015447 7.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_152383 DIS3L2 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs7571816 9.00E-09 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_152383 DIS3L2 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Body Height rs6717918 3.00E-09 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_152383 DIS3L2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs749052 1.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_152383 DIS3L2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2580816 6.00E-22 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_152390 TMEM178 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs2716734 2.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_152390 TMEM178 18957941 http://www.ncbi.nlm.nih.gov/pubmed/18957941 Personality rs2540226 3.00E-06 Genome-wide association scan for five major dimensions of personality. NHGRI|-1
NM_152396 METTL6 18759275 http://www.ncbi.nlm.nih.gov/pubmed/18759275 Uric Acid rs6442522 5.00E-06 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. NHGRI|-1
NM_152399 TMEM155 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 2" rs7659604 9.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_152402 TRAM1L1 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs10433903 3.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_152402 TRAM1L1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs4318720 8.00E-07 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_152402 TRAM1L1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs2389202 4.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_152403 EGFLAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs2956597 9.25E-06 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_152403 EGFLAM 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs270545 1.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_152404 UGT3A1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs860413 1.00E-11 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_152408 POC5 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2112347 2.00E-13 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_152410 PACRG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2206256 1.04E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_152410 PACRG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs11966842 2.88E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_152410 PACRG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs11966948 1.12E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_152410 PACRG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6904305 2.32E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_152411 ZNF786 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1405123 1.30E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_152415 VPS37A 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs3793427 2.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_152416 C8orf38 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs4392868 8.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_152416 C8orf38 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs7000734 4.00E-07 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_152417 TMEM68 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4738287 1.12E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_152417 TMEM68 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6988277 3.20E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_152417 TMEM68 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10107657 3.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_152417 TMEM68 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4738382 2.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_152424 FAM123B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2152466 1.49E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_152431 PIWIL4 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Attention Deficit Disorder with Hyperactivity rs2212361 9.00E-07 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_152434 CWF19L2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1490936 4.52E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_152437 ZNF664 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs4765078 1.67E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_152447 LRFN5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2415603 3.27E-06 NBL-GWAS version 2 dbGaP|2895
NM_152451 GCOM1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs937254 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_152451 GCOM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs935549 3.91E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_152451 GCOM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs744318 3.60E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_152453 TMCO5A 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs16966460 4.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_152453 TMCO5A 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs12148658 1.00E-04 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_152487 TMEM56 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1414896 2.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_152495 CNIH3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2662928 8.79E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_152495 CNIH3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs1892121 6.78E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_152498 WDR65 21460395 http://www.ncbi.nlm.nih.gov/pubmed/21460395 Telomere length rs621559 2.00E-06 A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer. NHGRI|-1
NM_152503 C20orf132 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs8115854 2.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_152503 C20orf132 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs6031882 6.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_152504 C20orf196 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs4815868 8.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_152510 HORMAD2 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 "Glomerulonephritis, IGA" rs2412971 2.00E-09 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_152510 HORMAD2 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory Bowel Diseases rs2412973 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_152511 DUSP18 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs5753271 4.35E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_152515 CKAP2L 20844546 http://www.ncbi.nlm.nih.gov/pubmed/20844546 Endometriosis rs6542095 3.00E-06 Meta-analysis of genome-wide association scans for genetic susceptibility to endometriosis in Japanese population. NHGRI|-1
NM_152515 CKAP2L 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11677416 7.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_152520 ZNF385B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs1517702 3.83E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_152520 ZNF385B 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs16866933 6.00E-14 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_152520 ZNF385B 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs4556941 8.69E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_152520 ZNF385B 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4556941 8.25E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_152526 PARD3B 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs2335704 2.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_152526 PARD3B 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2276677 8.56E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_152526 PARD3B 18471798 http://www.ncbi.nlm.nih.gov/pubmed/18471798 "Osteoarthritis, Knee" rs1207421 6.00E-06 Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis. NHGRI|-1
NM_152526 PARD3B 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs11884476 3.00E-09 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_152526 PARD3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7421114 9.89E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_152531 C3orf21 20876614 http://www.ncbi.nlm.nih.gov/pubmed/20876614 "Carcinoma, Non-Small-Cell Lung" rs2131877 2.00E-08 A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population. NHGRI|-1
NM_152531 C3orf21 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs3892715 6.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_152536 FGD5 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs294636 2.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_152538 IGSF11 17903300 http://www.ncbi.nlm.nih.gov/pubmed/17903300 Waist Circumference rs1875517 2.00E-06 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. NHGRI|-1
NM_152538 IGSF11 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs6438424 1.00E-13 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_152540 SCFD2 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs2898681 2.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_152542 PPM1K 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs893971 7.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_152544 C4orf23 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs1949733 8.00E-07 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NM_152545 RASGEF1B 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs710841 2.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_152545 RASGEF1B 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs710841 2.00E-08 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_152545 RASGEF1B 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs788867 9.00E-28 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_152554 C6orf195 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6911560 1.79E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_152556 C7orf60 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10229603 5.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_152557 ZNF746 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs855913 4.00E-08 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_152562 CDCA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4872354 5.99E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_152564 VPS13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4735627 2.26E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_152570 LINGO2 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10968576 3.00E-13 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_152570 LINGO2 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs12555345 5.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_152570 LINGO2 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs7029145 9.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_152572 C9orf98 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs11243897 6.00E-08 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_152573 RASEF 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Alanine Transaminase rs1998303 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_152574 TTC39B 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs471364 3.00E-10 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_152574 TTC39B 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs643531 7.00E-09 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_152574 TTC39B 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs1780159 6.00E-06 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_152577 ZNF645 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs5925696 3.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_152587 C11orf65 21186350 http://www.ncbi.nlm.nih.gov/pubmed/21186350 Metformin rs11212617 3.00E-09 Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. NHGRI|-1
NM_152588 TMTC2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs7298326 9.74E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_152590 IFLTD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4963910 8.37E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_152591 CCDC63 21270382 http://www.ncbi.nlm.nih.gov/pubmed/21270382 Alcohol Drinking rs10849915 1.00E-23 Genome-wide association studies identify genetic loci related to alcohol consumption in Korean men. NHGRI|-1
NM_152591 CCDC63 21372407 http://www.ncbi.nlm.nih.gov/pubmed/21372407 Drinking Behavior rs10774610 9.00E-120 Confirmation of ALDH2 as a Major locus of drinking behavior and of its variants regulating multiple metabolic phenotypes in a Japanese population. NHGRI|-1
NM_152594 SPRED1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs16966460 4.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_152597 FSIP1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs8033957 3.77E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_152598 10-Mar 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs2251393 4.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_152611 LRRN4 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs2326679 2.00E-06 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_152615 PARP15 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs2650951 1.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_152616 TRIM42 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs908821 1.40E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_152616 TRIM42 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs908821 3.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_152625 ZNF366 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10515148 6.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_152629 GLIS3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10491899 1.52E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_152629 GLIS3 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs7034200 1.00E-12 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_152629 GLIS3 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs7034200 1.00E-13 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_152629 GLIS3 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs7020673 5.00E-12 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_152629 GLIS3 18840781 http://www.ncbi.nlm.nih.gov/pubmed/18840781 "Diabetes Mellitus, Type 1" rs10758593 3.00E-06 Follow-up analysis of genome-wide association data identifies novel loci for type 1 diabetes. NHGRI|-1
NM_152638 C12orf12 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Magnesium rs7965584 1.00E-16 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_152638 C12orf12 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs10858945 6.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_152638 C12orf12 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs1847461 8.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_152640 DCP1B 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12423058 2.81E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_152647 C15orf33 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs4338740 1.00E-12 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_152647 C15orf33 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs4338740 3.00E-13 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NM_152649 MLKL 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7196369 2.05E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_152676 FBXO15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8086078 1.26E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_152676 FBXO15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8086078 3.24E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_152676 FBXO15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3813108 9.00E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_152688 KHDRBS2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Aspartate Aminotransferases rs6455128 3.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_152688 KHDRBS2 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs682238 3.00E-06 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_152688 KHDRBS2 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs9500256 5.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_152697 SLC44A5 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs1857353 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_152705 POLR1D 21471979 http://www.ncbi.nlm.nih.gov/pubmed/21471979 "Lymphoma, Large B-Cell, Diffuse" rs7097 7.00E-06 Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility. NHGRI|-1
NM_152706 C7orf62 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2724463 2.17E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_152717 MS4A15 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs7930940 2.00E-10 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_152721 DOK6 20548944 http://www.ncbi.nlm.nih.gov/pubmed/20548944 Osteoporosis rs17184557 9.00E-07 An integration of genome-wide association study and gene expression profiling to prioritize the discovery of novel susceptibility Loci for osteoporosis-related traits. NHGRI|-1
NM_152721 DOK6 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs893001 1.00E-10 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_152725 SLC39A12 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17661538 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_152725 SLC39A12 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4748442 9.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_152729 NT5DC1 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs1999930 1.00E-08 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_152730 C6orf170 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognition rs1343075 2.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_152733 BTBD9 17637780 http://www.ncbi.nlm.nih.gov/pubmed/17637780 Restless Legs Syndrome rs9296249 4.00E-18 Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. NHGRI|-1
NM_152733 BTBD9 17634447 http://www.ncbi.nlm.nih.gov/pubmed/17634447 Restless Legs Syndrome rs3923809 1.00E-17 A genetic risk factor for periodic limb movements in sleep. NHGRI|-1
NM_152735 ZBTB9 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs9394152 7.00E-08 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_152735 ZBTB9 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs9296092 6.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_152737 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12333130 5.60E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_152737 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1003024 6.43E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_152737 RNF182 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs1003024 7.51E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_152737 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1555051 7.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_152737 RNF182 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs7750009 7.53E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_152740 HIBADH 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs13225783 7.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_152744 SDK1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Thyrotropin rs6462411 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_152744 SDK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs882362 6.07E-05 NBL-GWAS version 2 dbGaP|2895
NM_152745 NXPH1 18762592 http://www.ncbi.nlm.nih.gov/pubmed/18762592 Neurotic Disorders rs2349775 7.00E-06 Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism. NHGRI|-1
NM_152745 NXPH1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1013812 3.32E-05 NBL-GWAS version 2 dbGaP|2895
NM_152745 NXPH1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10253965 5.41E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_152750 CDHR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs6967330 8.43E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_152750 CDHR3 20833655 http://www.ncbi.nlm.nih.gov/pubmed/20833655 Warfarin rs10270308 6.00E-06 Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. NHGRI|-1
NM_152754 SEMA3D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6972995 9.07E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_152754 SEMA3D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10277279 1.07E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_152754 SEMA3D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10277279 6.93E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_152754 SEMA3D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs782895 1.15E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_152760 SNX32 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7114014 2.27E-05 NBL-GWAS version 2 dbGaP|2895
NM_152774 TMEM196 17903292 http://www.ncbi.nlm.nih.gov/pubmed/17903292 Thyrotropin rs6977660 4.00E-06 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_152782 SUN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2708909 3.44E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_152787 TAB3 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs5971535 8.37E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_152788 ANKS1B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7968606 3.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_152788 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs2373011 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_152788 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs2373011 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_152788 ANKS1B 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11110077 4.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_152829 TES 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs1464776 1.55E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_152829 TES 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12673240 8.31E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_152830 ACE 20066004 http://www.ncbi.nlm.nih.gov/pubmed/20066004 Angiotensin-Converting Enzyme Inhibitors rs4343 3.00E-25 A genome-wide association study identifies new loci for ACE activity: potential implications for response to ACE inhibitor. NHGRI|-1
NM_152834 TMEM18 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1316288 1.03E-04 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_152834 TMEM18 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs2947411 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_152834 TMEM18 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs2867125 3.00E-49 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_152834 TMEM18 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs6548238 1.00E-18 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_152834 TMEM18 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs7561317 4.00E-17 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_152834 TMEM18 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7561317 2.00E-18 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_152851 MS4A6A 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs610932 2.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_152852 MS4A6A 21460840 http://www.ncbi.nlm.nih.gov/pubmed/21460840 Alzheimer Disease rs610932 2.00E-14 "Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease." NHGRI|-1
NM_152854 CD40 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs4810485 3.00E-09 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_152854 CD40 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 "Arthritis, Rheumatoid" rs4810485 8.00E-09 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_152854 CD40 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs6074022 1.00E-07 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_152855 IGLL1 21448238 http://www.ncbi.nlm.nih.gov/pubmed/21448238 Migraine without Aura rs140174 8.00E-06 Meta-analysis of genome-wide association for migraine in six population-based European cohorts. NHGRI|-1
NM_152855 IGLL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs6519442 1.55E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_152855 IGLL1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6519442 1.49E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_152857 WTAP 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs4516970 1.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_152858 WTAP 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs4516970 1.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_152860 SP7 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs2016266 1.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_152860 SP7 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs10876432 1.00E-07 New sequence variants associated with bone mineral density. NHGRI|-1
NM_152871 FAS 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs2234978 6.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_152871 FAS 21041692 http://www.ncbi.nlm.nih.gov/pubmed/21041692 Heart Function Tests rs1937332 7.00E-07 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. NHGRI|-1
NM_152871 FAS 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs11203032 8.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_152872 FAS 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs2234978 6.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_152872 FAS 21041692 http://www.ncbi.nlm.nih.gov/pubmed/21041692 Heart Function Tests rs1937332 7.00E-07 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. NHGRI|-1
NM_152872 FAS 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs11203032 8.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_152879 DGKD 20705733 http://www.ncbi.nlm.nih.gov/pubmed/20705733 Calcium rs838705 9.00E-06 Common variants in the calcium-sensing receptor gene are associated with total serum calcium levels. NHGRI|-1
NM_152888 COL22A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4545143 1.34E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_152888 COL22A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4556079 4.79E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_152888 COL22A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11781101 5.31E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_152888 COL22A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7004938 2.97E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_152888 COL22A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11783351 5.51E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_152888 COL22A1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4736239 7.42E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_152888 COL22A1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs13270196 2.27E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_152888 COL22A1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs994770 2.78E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_152888 COL22A1 21700879 http://www.ncbi.nlm.nih.gov/pubmed/21700879 Adiponectin rs2468677 8.00E-07 Novel Locus FER Is Associated With Serum HMW Adiponectin Levels. NHGRI|-1
NM_152898 FERD3L 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2192476 4.92E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_152910 DGKH 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs6561030 7.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_152910 DGKH 17486107 http://www.ncbi.nlm.nih.gov/pubmed/17486107 Bipolar Disorder rs1012053 2.00E-08 A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder. NHGRI|-1
NM_152910 DGKH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1886811 2.38E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_152912 MTIF3 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs4771122 9.00E-10 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_152912 MTIF3 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7336332 1.00E-06 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_152912 MTIF3 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs9512730 5.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_152912 MTIF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1218897 2.49E-05 NBL-GWAS version 2 dbGaP|2895
NM_152912 MTIF3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1218885 4.54E-05 NBL-GWAS version 2 dbGaP|2895
NM_152989 SOX5 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs7979575 2.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_152989 SOX5 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs1464500 1.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_152989 SOX5 19754311 http://www.ncbi.nlm.nih.gov/pubmed/19754311 Acquired Immunodeficiency Syndrome rs1522232 2.00E-06 Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). NHGRI|-1
NM_152989 SOX5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs550338 8.88E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_152989 SOX5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11046688 4.39E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_152996 ST6GALNAC3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs10873876 4.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_152996 ST6GALNAC3 20691247 http://www.ncbi.nlm.nih.gov/pubmed/20691247 Personality rs12753569 8.00E-06 A genome-wide association study of Cloninger's temperament scales: implications for the evolutionary genetics of personality. NHGRI|-1
NM_153000 APCDD1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7228911 6.74E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_153000 APCDD1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7228911 9.02E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_153002 GPR156 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs9289143 3.03E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_153002 GPR156 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs9289143 8.56E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_153005 RIOK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs9379104 6.63E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_153015 TMEM74 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs4735076 1.93E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_153021 PLB1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs2338545 6.34E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_153021 PLB1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2940787 1.92E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_153023 SPATA13 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2793483 3.78E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_153023 SPATA13 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17464589 2.84E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_153023 SPATA13 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs17079773 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_153026 PRICKLE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6582406 1.21E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_153026 PRICKLE1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7964774 8.92E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_153026 PRICKLE1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12427230 9.89E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_153026 PRICKLE1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4590936 7.68E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_153033 KCTD7 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs10263935 4.00E-07 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NM_153040 C15orf32 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs8040009 3.00E-07 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_153040 C15orf32 20386566 http://www.ncbi.nlm.nih.gov/pubmed/20386566 Bipolar Disorder rs8040009 6.00E-06 Genome-wide association study of bipolar I disorder in the Han Chinese population. NHGRI|-1
NM_153040 C15orf32 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Vital Capacity rs1455782 4.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_153045 C9orf91 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs10114470 4.08E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_153046 TDRD9 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Bipolar Disorder rs11622475 8.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_153050 MTMR3 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs36600 6.00E-13 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_153051 MTMR3 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs36600 6.00E-13 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_153184 CADM2 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs13078807 4.00E-11 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_153184 CADM2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7642134 4.00E-10 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_153184 CADM2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4574309 5.23E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_153184 CADM2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4396907 6.68E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_153184 CADM2 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs10511089 7.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_153187 SLC22A1 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs651164 2.00E-10 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_153187 SLC22A1 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs651164 2.00E-09 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_153217 TMEM174 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs7702331 6.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_153218 C13orf31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3764147 7.36E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_153218 C13orf31 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs3764147 2.00E-13 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_153218 C13orf31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs3764147 1.21E-10 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_153218 C13orf31 20018961 http://www.ncbi.nlm.nih.gov/pubmed/20018961 Leprosy rs3764147 4.00E-54 Genomewide association study of leprosy. NHGRI|-1
NM_153218 C13orf31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2121037 4.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_153218 C13orf31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs10507522 1.33E-08 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_153218 C13orf31 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs687582 6.19E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_153221 CILP2 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs16996148 3.00E-08 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_153221 CILP2 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs16996148 3.00E-09 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_153221 CILP2 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs16996148 4.00E-09 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_153221 CILP2 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs17216525 4.00E-11 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_153223 CEP120 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs2115172 2.00E-06 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_153223 CEP120 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aorta rs17470137 1.00E-11 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_153228 ANKFN1 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs1019238 6.00E-07 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_153228 ANKFN1 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs12449568 2.00E-06 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_153228 ANKFN1 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs17760296 7.00E-06 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_153228 ANKFN1 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs1431318 9.00E-07 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_153228 ANKFN1 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs8065311 2.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_153246 C6orf223 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6905288 2.00E-26 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_153246 C6orf223 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs943072 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_153246 C6orf223 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs881858 9.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_153246 C6orf223 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs9472138 4.00E-06 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_153246 C6orf223 21665990 http://www.ncbi.nlm.nih.gov/pubmed/21665990 Macular Degeneration rs4711751 9.00E-09 Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration. NHGRI|-1
NM_153267 MAMDC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs867595 8.33E-05 NBL-GWAS version 2 dbGaP|2895
NM_153267 MAMDC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs3015182 8.79E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_153267 MAMDC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2975868 8.99E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_153267 MAMDC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10511979 5.76E-05 NBL-GWAS version 2 dbGaP|2895
NM_153281 HYAL1 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs11130248 5.00E-07 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_153282 HYAL1 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs11130248 5.00E-07 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_153283 HYAL1 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs11130248 5.00E-07 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_153285 HYAL1 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs11130248 5.00E-07 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_153337 SNX20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9302752 1.45E-12 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_153337 SNX20 20018961 http://www.ncbi.nlm.nih.gov/pubmed/20018961 Leprosy rs9302752 4.00E-40 Genomewide association study of leprosy. NHGRI|-1
NM_153337 SNX20 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs7194886 1.41E-07 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_153337 SNX20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs7194886 2.42E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_153340 ATXN7L2 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs12049330 6.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_153355 NKAIN2 20634892 http://www.ncbi.nlm.nih.gov/pubmed/20634892 Neurotic Disorders rs9491140 3.00E-07 A genome-wide association study of neuroticism in a population-based sample. NHGRI|-1
NM_153355 NKAIN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs781484 1.83E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_153360 APCDD1L 20838585 http://www.ncbi.nlm.nih.gov/pubmed/20838585 Waist Circumference rs127430 1.00E-06 Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. NHGRI|-1
NM_153360 APCDD1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6026398 1.73E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_153363 ZNF679 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, LDL" rs10266483 8.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_153366 SVEP1 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs1327533 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_153366 SVEP1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs7042161 6.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_153367 ZCCHC24 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2145998 4.00E-13 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_153370 PI16 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs1405069 6.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NM_153371 LNX2 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7336332 1.00E-06 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_153371 LNX2 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs9512730 5.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_153371 LNX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1218897 2.49E-05 NBL-GWAS version 2 dbGaP|2895
NM_153371 LNX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1218885 4.54E-05 NBL-GWAS version 2 dbGaP|2895
NM_153377 LRIG3 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs11172782 7.00E-08 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_153378 SLC22A12 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs505802 2.00E-09 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_153426 PITX2 19597492 http://www.ncbi.nlm.nih.gov/pubmed/19597492 Atrial Fibrillation rs17042171 4.00E-63 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. NHGRI|-1
NM_153426 PITX2 19597491 http://www.ncbi.nlm.nih.gov/pubmed/19597491 Atrial Fibrillation rs2200733 1.00E-14 A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. NHGRI|-1
NM_153426 PITX2 17603472 http://www.ncbi.nlm.nih.gov/pubmed/17603472 Atrial Fibrillation rs2200733 3.00E-41 Variants conferring risk of atrial fibrillation on chromosome 4q25. NHGRI|-1
NM_153426 PITX2 18991354 http://www.ncbi.nlm.nih.gov/pubmed/18991354 Stroke rs2200733 2.00E-10 Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. NHGRI|-1
NM_153426 PITX2 20173747 http://www.ncbi.nlm.nih.gov/pubmed/20173747 Atrial Fibrillation rs6843082 3.00E-28 Common variants in KCNN3 are associated with lone atrial fibrillation. NHGRI|-1
NM_153426 PITX2 17603472 http://www.ncbi.nlm.nih.gov/pubmed/17603472 Atrial Fibrillation rs10033464 7.00E-11 Variants conferring risk of atrial fibrillation on chromosome 4q25. NHGRI|-1
NM_153426 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs10033464 5.70E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_153426 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2654735 9.03E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_153426 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1806506 3.67E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_153427 PITX2 19597492 http://www.ncbi.nlm.nih.gov/pubmed/19597492 Atrial Fibrillation rs17042171 4.00E-63 Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. NHGRI|-1
NM_153427 PITX2 19597491 http://www.ncbi.nlm.nih.gov/pubmed/19597491 Atrial Fibrillation rs2200733 1.00E-14 A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. NHGRI|-1
NM_153427 PITX2 17603472 http://www.ncbi.nlm.nih.gov/pubmed/17603472 Atrial Fibrillation rs2200733 3.00E-41 Variants conferring risk of atrial fibrillation on chromosome 4q25. NHGRI|-1
NM_153427 PITX2 18991354 http://www.ncbi.nlm.nih.gov/pubmed/18991354 Stroke rs2200733 2.00E-10 Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke. NHGRI|-1
NM_153427 PITX2 20173747 http://www.ncbi.nlm.nih.gov/pubmed/20173747 Atrial Fibrillation rs6843082 3.00E-28 Common variants in KCNN3 are associated with lone atrial fibrillation. NHGRI|-1
NM_153427 PITX2 17603472 http://www.ncbi.nlm.nih.gov/pubmed/17603472 Atrial Fibrillation rs10033464 7.00E-11 Variants conferring risk of atrial fibrillation on chromosome 4q25. NHGRI|-1
NM_153427 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Myocardial Infarction rs10033464 5.70E-04 Genome-wide association between genotype and incident myocardial infarction in CHS participants of primary self-described European ancestry dbGaP|2873
NM_153427 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2654735 9.03E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_153427 PITX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1806506 3.67E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_153442 GPR26 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs10510126 2.57E-06 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_153442 GPR26 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs17663978 4.84E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_153442 GPR26 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7916600 1.16E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_153449 SLC2A14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1894829 6.24E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_153449 SLC2A14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1894829 8.02E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_153449 SLC2A14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11612319 4.41E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_153449 SLC2A14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11612319 6.55E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_153449 SLC2A14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10047605 2.60E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_153456 HS6ST3 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs2038823 5.00E-11 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_153498 CAMK1D 20862305 http://www.ncbi.nlm.nih.gov/pubmed/20862305 "Diabetes Mellitus, Type 2" rs10906115 1.00E-08 Identification of new genetic risk variants for type 2 diabetes. NHGRI|-1
NM_153498 CAMK1D 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs12779790 1.00E-10 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_153498 CAMK1D 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11257695 1.67E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_153498 CAMK1D 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11257695 5.30E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_153604 MYOCD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs8068445 1.10E-05 NBL-GWAS version 2 dbGaP|2895
NM_153607 C5orf41 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs251253 9.00E-13 Genome-wide association study of PR interval. NHGRI|-1
NM_153609 TMPRSS6 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Erythrocyte Indices rs855791 1.00E-10 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_153609 TMPRSS6 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs855791 1.00E-12 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_153609 TMPRSS6 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs855791 3.00E-25 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_153609 TMPRSS6 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs855791 5.00E-09 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_153609 TMPRSS6 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs855791 3.00E-14 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_153609 TMPRSS6 19820698 http://www.ncbi.nlm.nih.gov/pubmed/19820698 Hemoglobins rs855791 2.00E-13 Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels. NHGRI|-1
NM_153609 TMPRSS6 19820699 http://www.ncbi.nlm.nih.gov/pubmed/19820699 Hemoglobins rs855791 5.00E-07 Common variants in TMPRSS6 are associated with iron status and erythrocyte volume. NHGRI|-1
NM_153609 TMPRSS6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs855791 3.93E-07 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_153609 TMPRSS6 21149283 http://www.ncbi.nlm.nih.gov/pubmed/21149283 Iron-Regulatory Proteins rs855791 2.00E-15 Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. NHGRI|-1
NM_153609 TMPRSS6 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs5756506 1.00E-09 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_153609 TMPRSS6 20927387 http://www.ncbi.nlm.nih.gov/pubmed/20927387 Erythrocyte Indices rs4820268 1.00E-12 A genome-wide association study of red blood cell traits using the electronic medical record. NHGRI|-1
NM_153609 TMPRSS6 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs4820268 3.00E-10 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_153609 TMPRSS6 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Erythrocyte Indices rs4820268 4.00E-12 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_153609 TMPRSS6 21208937 http://www.ncbi.nlm.nih.gov/pubmed/21208937 Iron rs4820268 4.00E-11 Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels. NHGRI|-1
NM_153609 TMPRSS6 19880490 http://www.ncbi.nlm.nih.gov/pubmed/19880490 Iron rs4820268 5.00E-09 A genome-wide association analysis of serum iron concentrations. NHGRI|-1
NM_153609 TMPRSS6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs4820268 6.00E-07 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_153609 TMPRSS6 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Iron rs4820268 6.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_153609 TMPRSS6 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs2413450 3.00E-41 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_153609 TMPRSS6 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs2413450 9.00E-34 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_153609 TMPRSS6 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs2413450 2.00E-13 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_153609 TMPRSS6 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs228907 5.17E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_153610 CMYA5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7735699 1.78E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_153610 CMYA5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs265010 2.67E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_153616 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs12594515 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_153616 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs12594515 7.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_153616 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4603502 3.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_153616 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1865648 1.57E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_153616 SEMA6D 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11857760 6.14E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_153617 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs12594515 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_153617 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs12594515 7.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_153617 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4603502 3.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_153617 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1865648 1.57E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_153617 SEMA6D 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11857760 6.14E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_153618 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs12594515 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_153618 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs12594515 7.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_153618 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4603502 3.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_153618 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1865648 1.57E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_153618 SEMA6D 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11857760 6.14E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_153619 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs12594515 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_153619 SEMA6D 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs12594515 7.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_153619 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4603502 3.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_153619 SEMA6D 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1865648 1.57E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_153619 SEMA6D 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11857760 6.14E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_153634 CPNE8 19483685 http://www.ncbi.nlm.nih.gov/pubmed/19483685 Drug-Induced Liver Injury rs6582630 1.00E-06 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. NHGRI|-1
NM_153636 CPNE7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs154659 7.56E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_153636 CPNE7 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs154659 7.00E-08 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_153646 SLC24A4 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs4904947 8.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_153646 SLC24A4 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs1009170 2.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_153646 SLC24A4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs12896399 1.00E-16 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_153646 SLC24A4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs12896399 2.00E-23 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_153646 SLC24A4 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Eye Color rs12896399 4.00E-38 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_153646 SLC24A4 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Hair Color rs12896399 1.00E-48 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_153646 SLC24A4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12896399 5.00E-13 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_153646 SLC24A4 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs12896399 8.00E-21 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_153647 SLC24A4 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs4904947 8.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_153647 SLC24A4 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs1009170 2.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_153647 SLC24A4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs12896399 1.00E-16 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_153647 SLC24A4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs12896399 2.00E-23 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_153647 SLC24A4 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Eye Color rs12896399 4.00E-38 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_153647 SLC24A4 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Hair Color rs12896399 1.00E-48 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_153647 SLC24A4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12896399 5.00E-13 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_153647 SLC24A4 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs12896399 8.00E-21 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_153648 SLC24A4 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs4904947 8.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_153648 SLC24A4 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs1009170 2.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_153648 SLC24A4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs12896399 1.00E-16 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_153648 SLC24A4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs12896399 2.00E-23 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_153648 SLC24A4 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Eye Color rs12896399 4.00E-38 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_153648 SLC24A4 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Hair Color rs12896399 1.00E-48 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NM_153648 SLC24A4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12896399 5.00E-13 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_153648 SLC24A4 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs12896399 8.00E-21 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NM_153686 LCORL 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs16896068 2.00E-13 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_153686 LCORL 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs6830062 1.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_153686 LCORL 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs6830062 5.00E-09 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_153686 LCORL 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs6830062 8.00E-06 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_153689 C2orf69 21573128 http://www.ncbi.nlm.nih.gov/pubmed/21573128 Osteoporosis rs7605378 2.00E-08 "Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese." NHGRI|-1
NM_153690 FAM43A 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs3892715 6.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_153702 ELMOD2 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Bilirubin rs1594468 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_153710 C9orf96 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs28602591 1.00E-11 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_153714 C10orf67 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10734046 6.23E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_153714 C10orf67 18723019 http://www.ncbi.nlm.nih.gov/pubmed/18723019 Crohn Disease rs1398024 4.00E-06 Genome-wide association analysis in sarcoidosis and Crohn's disease unravels a common susceptibility locus on 10p12.2. NHGRI|-1
NM_153742 CTH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_153742 CTH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 8.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_153742 CTH 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs10458561 4.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NM_153746 ZDHHC14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9365242 6.70E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_153746 ZDHHC14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9365243 4.53E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_153746 ZDHHC14 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6903041 1.19E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_153759 DNMT3A 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs13428812 9.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_153764 KCNJ1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs588407 3.45E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_153765 KCNJ1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs588407 3.45E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_153766 KCNJ1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs588407 3.45E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_153767 KCNJ1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs588407 3.45E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_153810 C10orf46 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10886289 6.41E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_153815 RASGRF1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs3743195 4.06E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_153815 RASGRF1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs3743200 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_153815 RASGRF1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs3816282 2.16E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_153815 RASGRF1 20835236 http://www.ncbi.nlm.nih.gov/pubmed/20835236 Myopia rs939658 2.00E-09 A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25. NHGRI|-1
NM_156039 CSF3R 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7549591 7.93E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_170601 SIAE 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs544368 6.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_170604 RASGRP4 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger Syndrome rs892055 5.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_170606 MLL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs56500751 3.37E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_170662 CBLB 20453840 http://www.ncbi.nlm.nih.gov/pubmed/20453840 Multiple Sclerosis rs9657904 2.00E-10 Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis. NHGRI|-1
NM_170662 CBLB 21668797 http://www.ncbi.nlm.nih.gov/pubmed/21668797 Marijuana Abuse rs12491921 1.00E-06 A genome-wide association study of DSM-IV cannabis dependence. NHGRI|-1
NM_170664 OTOA 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs8050407 2.20E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_170665 ATP2A2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Alpha-Globulins rs11065611 1.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_170672 RASGRP3 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs13385731 1.00E-15 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_170674 MEIS2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs8041675 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_170674 MEIS2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs1568679 1.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_170675 MEIS2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs8041675 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_170675 MEIS2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs1568679 1.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_170676 MEIS2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs8041675 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_170676 MEIS2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs1568679 1.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_170677 MEIS2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs8041675 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_170677 MEIS2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs1568679 1.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_170695 TGIF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs431220 5.88E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_170696 ALDH1A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs597804 5.59E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_170696 ALDH1A2 19609347 http://www.ncbi.nlm.nih.gov/pubmed/19609347 Hypertension rs1550576 3.00E-06 A genome-wide association study of hypertension and blood pressure in African Americans. NHGRI|-1
NM_170697 ALDH1A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs597804 5.59E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_170697 ALDH1A2 19609347 http://www.ncbi.nlm.nih.gov/pubmed/19609347 Hypertension rs1550576 3.00E-06 A genome-wide association study of hypertension and blood pressure in African Americans. NHGRI|-1
NM_170711 DAZAP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7251833 4.67E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_170721 MSI2 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs792376 2.00E-07 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_170724 PKHD1 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Prostatic Neoplasms rs10498792 3.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_170724 PKHD1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs6935568 7.44E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_170731 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170731 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170731 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_170731 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_170732 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170732 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170732 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_170732 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_170733 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170733 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170733 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_170733 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_170734 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170734 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170734 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_170734 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_170735 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs6265 5.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170735 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs6265 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170735 BDNF 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs6265 2.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NM_170735 BDNF 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10767664 5.00E-26 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_170738 MRPL11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1791682 1.08E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_170739 MRPL11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1791682 1.08E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_170743 IL28RA 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs4649203 7.00E-08 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_170744 UNC5B 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs16928529 4.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_170744 UNC5B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10999637 7.46E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_170744 UNC5B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4746077 3.35E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_170744 UNC5B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4456181 6.13E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_170744 UNC5B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4456181 7.32E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_170769 RNF39 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs9261290 1.73E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_170769 RNF39 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4711209 1.03E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_170769 RNF39 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs916570 1.10E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_170775 KCNN2 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 "Anemia, Sickle Cell" rs17135859 8.00E-06 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_170775 KCNN2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs4621553 4.00E-08 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_170782 KCNN3 20173747 http://www.ncbi.nlm.nih.gov/pubmed/20173747 Atrial Fibrillation rs13376333 2.00E-21 Common variants in KCNN3 are associated with lone atrial fibrillation. NHGRI|-1
NM_170783 ZNRD1 19115949 http://www.ncbi.nlm.nih.gov/pubmed/19115949 Acquired Immunodeficiency Syndrome rs8321 5.00E-07 Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). NHGRI|-1
NM_170783 ZNRD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs8321 6.18E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_171999 SALL3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs594821 4.32E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_171999 SALL3 18668548 http://www.ncbi.nlm.nih.gov/pubmed/18668548 "Arthritis, Rheumatoid" rs2002842 6.00E-06 Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility. NHGRI|-1
NM_172004 CLECL1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs11052552 7.00E-07 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_172037 RDH10 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs12679254 2.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_172037 RDH10 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs10283372 1.90E-05 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_172056 KCNH2 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3807375 5.00E-11 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_172056 KCNH2 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs2968864 8.00E-16 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_172056 KCNH2 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs2968863 2.00E-15 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_172056 KCNH2 20062061 http://www.ncbi.nlm.nih.gov/pubmed/20062061 Electrocardiography rs4725982 3.00E-06 Genetic variation in SCN10A influences cardiac conduction. NHGRI|-1
NM_172056 KCNH2 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs4725982 5.00E-16 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_172057 KCNH2 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3807375 5.00E-11 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_172057 KCNH2 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs2968864 8.00E-16 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_172057 KCNH2 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs2968863 2.00E-15 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_172057 KCNH2 20062061 http://www.ncbi.nlm.nih.gov/pubmed/20062061 Electrocardiography rs4725982 3.00E-06 Genetic variation in SCN10A influences cardiac conduction. NHGRI|-1
NM_172057 KCNH2 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs4725982 5.00E-16 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_172058 EYA1 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs2218488 3.00E-06 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_172059 EYA1 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs2218488 3.00E-06 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_172060 EYA1 17903308 http://www.ncbi.nlm.nih.gov/pubmed/17903308 Sleep rs2218488 3.00E-06 Genome-wide association of sleep and circadian phenotypes. NHGRI|-1
NM_172070 UBR3 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10204475 5.36E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_172101 CD8B 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs6547705 1.00E-08 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_172102 CD8B 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs6547705 1.00E-08 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_172103 EYA4 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 alpha-Macroglobulins rs9402515 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_172103 EYA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs9402515 8.86E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_172103 EYA4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4487594 1.06E-06 NBL-GWAS version 1 dbGaP|2845
NM_172103 EYA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4487594 2.88E-06 NBL-GWAS version 2 dbGaP|2895
NM_172105 EYA4 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 alpha-Macroglobulins rs9402515 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_172105 EYA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs9402515 8.86E-04 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_172105 EYA4 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4487594 1.06E-06 NBL-GWAS version 1 dbGaP|2845
NM_172105 EYA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4487594 2.88E-06 NBL-GWAS version 2 dbGaP|2895
NM_172114 CAMK2D 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs13134836 2.84E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_172114 CAMK2D 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12331375 1.11E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_172115 CAMK2D 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs13134836 2.84E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_172115 CAMK2D 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12331375 1.11E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_172127 CAMK2D 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs13134836 2.84E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_172127 CAMK2D 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12331375 1.11E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_172128 CAMK2D 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs13134836 2.84E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_172128 CAMK2D 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12331375 1.11E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_172129 CAMK2D 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs13134836 2.84E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_172129 CAMK2D 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12331375 1.11E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_172138 IL28A 19684573 http://www.ncbi.nlm.nih.gov/pubmed/19684573 Hepatitis C rs12979860 1.00E-28 Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance. NHGRI|-1
NM_172138 IL28A 21228123 http://www.ncbi.nlm.nih.gov/pubmed/21228123 Hepatitis C rs8099917 1.00E-20 IL-28B predicts response to chronic hepatitis C therapy--fine-mapping and replication study in Asian populations. NHGRI|-1
NM_172138 IL28A 19749757 http://www.ncbi.nlm.nih.gov/pubmed/19749757 Hepatitis C rs8099917 3.00E-32 Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C. NHGRI|-1
NM_172138 IL28A 20060832 http://www.ncbi.nlm.nih.gov/pubmed/20060832 Hepatitis C rs8099917 6.00E-09 Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study. NHGRI|-1
NM_172138 IL28A 19749758 http://www.ncbi.nlm.nih.gov/pubmed/19749758 Hepatitis C rs8099917 9.00E-09 IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy. NHGRI|-1
NM_172139 IL28B 19684573 http://www.ncbi.nlm.nih.gov/pubmed/19684573 Hepatitis C rs12979860 1.00E-28 Genetic variation in IL28B predicts hepatitis C treatment-induced viral clearance. NHGRI|-1
NM_172139 IL28B 21228123 http://www.ncbi.nlm.nih.gov/pubmed/21228123 Hepatitis C rs8099917 1.00E-20 IL-28B predicts response to chronic hepatitis C therapy--fine-mapping and replication study in Asian populations. NHGRI|-1
NM_172139 IL28B 19749757 http://www.ncbi.nlm.nih.gov/pubmed/19749757 Hepatitis C rs8099917 3.00E-32 Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C. NHGRI|-1
NM_172139 IL28B 20060832 http://www.ncbi.nlm.nih.gov/pubmed/20060832 Hepatitis C rs8099917 6.00E-09 Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study. NHGRI|-1
NM_172139 IL28B 19749758 http://www.ncbi.nlm.nih.gov/pubmed/19749758 Hepatitis C rs8099917 9.00E-09 IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy. NHGRI|-1
NM_172159 KCNAB1 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Aging rs3772255 8.00E-06 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_172160 KCNAB1 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Aging rs3772255 8.00E-06 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_172163 KCNQ4 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4660456 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_172165 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3749953 2.36E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_172165 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3131379 7.24E-85 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_172165 MSH5 18204446 http://www.ncbi.nlm.nih.gov/pubmed/18204446 "Lupus Erythematosus, Systemic" rs3131379 2.00E-52 "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci." NHGRI|-1
NM_172165 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3131379 4.89E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_172166 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3749953 2.36E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_172166 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3131379 7.24E-85 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_172166 MSH5 18204446 http://www.ncbi.nlm.nih.gov/pubmed/18204446 "Lupus Erythematosus, Systemic" rs3131379 2.00E-52 "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci." NHGRI|-1
NM_172166 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3131379 4.89E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_172174 IL15 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs17007695 9.00E-07 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_172174 IL15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs746484 6.98E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_172174 IL15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9308140 5.26E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_172174 IL15 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4267812 6.73E-06 NBL-GWAS version 1 dbGaP|2845
NM_172175 IL15 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs17007695 9.00E-07 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_172175 IL15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs746484 6.98E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_172175 IL15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9308140 5.26E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_172175 IL15 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4267812 6.73E-06 NBL-GWAS version 1 dbGaP|2845
NM_172197 AGER 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs8365 1.09E-17 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_172197 AGER 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs2070600 3.00E-14 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_172197 AGER 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs2070600 3.00E-15 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_172197 AGER 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs2070600 2.18E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_172198 KCND3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11102457 1.72E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_172201 KCNE2 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs9982601 4.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_172201 KCNE2 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs9982601 6.00E-11 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_172206 CAMKK1 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs758642 7.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_172207 CAMKK1 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs758642 7.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_172210 CSF1 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs10494112 7.00E-35 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_172210 CSF1 20436471 http://www.ncbi.nlm.nih.gov/pubmed/20436471 Osteitis Deformans rs484959 5.00E-24 "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone." NHGRI|-1
NM_172210 CSF1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs525566 5.88E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_172211 CSF1 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs10494112 7.00E-35 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_172211 CSF1 20436471 http://www.ncbi.nlm.nih.gov/pubmed/20436471 Osteitis Deformans rs484959 5.00E-24 "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone." NHGRI|-1
NM_172211 CSF1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs525566 5.88E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_172212 CSF1 21623375 http://www.ncbi.nlm.nih.gov/pubmed/21623375 Paget's disease rs10494112 7.00E-35 Genome-wide association identifies three new susceptibility loci for Paget's disease of bone. NHGRI|-1
NM_172212 CSF1 20436471 http://www.ncbi.nlm.nih.gov/pubmed/20436471 Osteitis Deformans rs484959 5.00E-24 "Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone." NHGRI|-1
NM_172212 CSF1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs525566 5.88E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_172213 CD8B 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs6547705 1.00E-08 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_172217 IL16 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs7172689 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_172219 CSF3 20172861 http://www.ncbi.nlm.nih.gov/pubmed/20172861 Leukocyte Count rs4794822 6.00E-10 Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count. NHGRI|-1
NM_172219 CSF3 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs4794822 4.00E-16 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_172220 CSF3 20172861 http://www.ncbi.nlm.nih.gov/pubmed/20172861 Leukocyte Count rs4794822 6.00E-10 Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count. NHGRI|-1
NM_172220 CSF3 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs4794822 4.00E-16 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_172231 SUGP1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs10401969 1.00E-11 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_172231 SUGP1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs10401969 2.00E-08 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_172232 ABCA5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs558076 2.53E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_172232 ABCA5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs817097 6.22E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_172238 TFAP2D 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2894779 2.25E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_172240 POC1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs770374 5.30E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_172241 CTAGE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4800370 8.92E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_172241 CTAGE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11664999 9.70E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_172244 SGCD 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Anthropometry rs157350 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_172244 SGCD 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Waist-Hip Ratio rs157350 6.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_172244 SGCD 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs4704970 7.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_172313 CSF3R 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7549591 7.93E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_172315 MEIS2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs8041675 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_172315 MEIS2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs1568679 1.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_172316 MEIS2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs8041675 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_172316 MEIS2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs1568679 1.00E-08 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_172364 CACNA2D4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4765864 1.24E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_172365 C14orf50 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2123461 1.66E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_172370 DAOA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9301037 4.12E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_172370 DAOA 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs4996815 1.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_172370 DAOA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs16968122 6.21E-06 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_172370 DAOA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs12428682 1.65E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_172370 DAOA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs9586708 1.74E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_172370 DAOA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs7139453 1.34E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_172370 DAOA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs4632004 1.30E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_172373 ELF1 21044949 http://www.ncbi.nlm.nih.gov/pubmed/21044949 "Lupus Erythematosus, Systemic" rs7329174 1.00E-08 ELF1 is associated with systemic lupus erythematosus in Asian populations. NHGRI|-1
NM_172375 KCNH5 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs973968 3.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_172375 KCNH5 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1514928 3.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_172376 KCNH5 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Transferrin rs973968 3.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_172376 KCNH5 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1514928 3.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_173054 RELN 18282107 http://www.ncbi.nlm.nih.gov/pubmed/18282107 Schizophrenia rs7341475 9.00E-07 Genome-wide association identifies a common variant in the reelin gene that increases the risk of schizophrenia only in women. NHGRI|-1
NM_173054 RELN 19230858 http://www.ncbi.nlm.nih.gov/pubmed/19230858 Otosclerosis rs3914132 2.00E-08 A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis. NHGRI|-1
NM_173054 RELN 20452100 http://www.ncbi.nlm.nih.gov/pubmed/20452100 Neurofibrillary Tangles rs4298437 2.00E-06 Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study. NHGRI|-1
NM_173054 RELN 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs17157903 1.03E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_173054 RELN 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs17157903 3.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_173059 ZAN 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Count rs2075671 1.00E-09 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_173060 CAST 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4434401 6.76E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_173060 CAST 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10053056 2.19E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_173060 CAST 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs27524 3.00E-11 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_173060 CAST 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9918149 4.77E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_173064 IL28RA 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs4649203 7.00E-08 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_173065 IL28RA 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs4649203 7.00E-08 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_173073 SLC35C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs12480667 1.90E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_173074 PIGF 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs17818399 3.00E-07 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_173076 ABCA12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs3795857 5.80E-06 NBL-GWAS version 2 dbGaP|2895
NM_173076 ABCA12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs11677798 2.38E-06 NBL-GWAS version 2 dbGaP|2895
NM_173076 ABCA12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2592232 8.87E-10 NBL-GWAS version 2 dbGaP|2895
NM_173076 ABCA12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10498025 5.45E-11 NBL-GWAS version 2 dbGaP|2895
NM_173076 ABCA12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10498026 9.69E-09 NBL-GWAS version 2 dbGaP|2895
NM_173076 ABCA12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1952224 1.77E-05 NBL-GWAS version 2 dbGaP|2895
NM_173081 ARMC3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7094187 1.14E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_173081 ARMC3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs6482235 2.25E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_173081 ARMC3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs17527491 8.44E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_173081 ARMC3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs7091875 2.17E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_173091 NFATC2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2143630 7.41E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_173159 NPAS3 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Mental Disorders rs4982029 4.00E-06 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_173159 NPAS3 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs8015959 5.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_173159 NPAS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs8014514 1.79E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_173159 NPAS3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17555909 6.53E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_173159 NPAS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17571355 2.92E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_173159 NPAS3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs10142154 2.34E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_173160 FXYD4 20598377 http://www.ncbi.nlm.nih.gov/pubmed/20598377 Multiple Sclerosis rs2503875 2.00E-07 Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. NHGRI|-1
NM_173161 IL1F10 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Interleukin 1 Receptor Antagonist Protein rs6761276 7.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_173161 IL1F10 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs6734238 2.00E-17 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_173162 KCNH7 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs17716942 1.00E-13 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_173162 KCNH7 19680635 http://www.ncbi.nlm.nih.gov/pubmed/19680635 "Parkinson Disease, Secondary" rs12476047 3.00E-06 Genome-wide association study of antipsychotic-induced parkinsonism severity among schizophrenia patients. NHGRI|-1
NM_173174 PTK2B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7833348 7.55E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_173175 PTK2B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7833348 7.55E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_173176 PTK2B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7833348 7.55E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_173177 C1D 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs724568 5.00E-06 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_173179 SLC35C2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs12480667 1.90E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_173207 TGIF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs431220 5.88E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_173208 TGIF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs431220 5.88E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_173209 TGIF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs431220 5.88E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_173210 TGIF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs431220 5.88E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_173211 TGIF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs431220 5.88E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_173214 NFAT5 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1364063 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_173216 ST6GAL1 19483685 http://www.ncbi.nlm.nih.gov/pubmed/19483685 Floxacillin rs10937275 1.00E-08 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. NHGRI|-1
NM_173217 ST6GAL1 19483685 http://www.ncbi.nlm.nih.gov/pubmed/19483685 Floxacillin rs10937275 1.00E-08 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. NHGRI|-1
NM_173343 IL1R2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4851526 4.39E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_173343 IL1R2 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2310173 3.00E-12 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_173343 IL1R2 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs2310173 5.00E-07 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_173344 ST3GAL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2978012 8.73E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_173344 ST3GAL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2978015 8.81E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_173344 ST3GAL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2978023 1.81E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_173352 KRT78 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs902774 5.00E-09 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_173355 UPP2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10183640 5.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_173359 EIF4E3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10460943 7.33E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_173464 L3MBTL4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs636589 5.89E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_173469 UBE2Q2 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Cystatin C rs1394125 3.00E-17 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_173474 NTAN1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs1136001 7.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_173488 SLCO6A1 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs1502844 1.00E-06 Common variants conferring risk of schizophrenia. NHGRI|-1
NM_173496 MPP7 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs927675 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_173499 SPATA8 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2045325 9.57E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_173499 SPATA8 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs4533251 4.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_173512 SLC38A11 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Foot rs776488 2.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_173512 SLC38A11 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs13424957 3.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_173514 SLC38A9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2897834 6.84E-05 NBL-GWAS version 2 dbGaP|2895
NM_173519 CLVS1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs903027 6.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_173528 C15orf26 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2663944 1.34E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_173528 C15orf26 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2683238 1.54E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_173528 C15orf26 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs1317060 3.89E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_173536 GABRG1 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body Mass Index rs10938397 3.00E-16 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_173536 GABRG1 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs10938397 4.00E-31 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_173536 GABRG1 21700879 http://www.ncbi.nlm.nih.gov/pubmed/21700879 Adiponectin rs10517133 5.00E-06 Novel Locus FER Is Associated With Serum HMW Adiponectin Levels. NHGRI|-1
NM_173538 CNBD1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1852027 7.62E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_173538 CNBD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2336981 5.01E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_173538 CNBD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7833568 3.55E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_173546 KLHDC8B 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7617480 3.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_173547 TRIM65 21681796 http://www.ncbi.nlm.nih.gov/pubmed/21681796 Cerebrum rs3744028 4.00E-15 Genome-wide association studies of cerebral white matter lesion burden: The CHARGE consortium. NHGRI|-1
NM_173549 C8orf47 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs13278732 6.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_173552 C3orf58 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs800082 3.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_173552 C3orf58 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Prostatic Neoplasms rs345013 5.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_173554 C10orf107 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Blood Pressure rs1530440 1.00E-09 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_173560 RFX6 20676098 http://www.ncbi.nlm.nih.gov/pubmed/20676098 Prostatic Neoplasms rs339331 2.00E-12 Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. NHGRI|-1
NM_173561 UNC5CL 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs10484761 7.00E-12 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NM_173598 KSR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs481745 1.52E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_173598 KSR2 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 "Cholesterol, LDL" rs4767631 6.00E-07 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_173598 KSR2 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Cholesterol rs10444502 6.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_173598 KSR2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7295696 1.77E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_173601 GXYLT1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2220999 1.09E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_173601 GXYLT1 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 "Cholesterol, HDL" rs871392 3.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_173601 GXYLT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11532502 1.30E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_173601 GXYLT1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10880174 5.06E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_173601 GXYLT1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10785303 5.06E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_173601 GXYLT1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs1472402 8.20E-06 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_173601 GXYLT1 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs978797 3.38E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_173602 DIP2B 20972440 http://www.ncbi.nlm.nih.gov/pubmed/20972440 Colorectal Neoplasms rs11169552 2.00E-10 "Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33." NHGRI|-1
NM_173611 FAM98B 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs11073328 2.00E-09 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_173615 VWA3A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs8058588 3.79E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_173622 CDRT4 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Forced Expiratory Volume rs2906966 8.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_173623 TTLL6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs8073596 7.62E-05 NBL-GWAS version 2 dbGaP|2895
NM_173647 RNF149 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs6711606 4.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_173653 SLC9A9 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs7632299 4.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_173653 SLC9A9 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs1371924 4.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_173653 SLC9A9 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs2800 3.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_173653 SLC9A9 20732626 http://www.ncbi.nlm.nih.gov/pubmed/20732626 Attention Deficit Disorder with Hyperactivity rs9810857 6.00E-06 Family-based genome-wide association scan of attention-deficit/hyperactivity disorder. NHGRI|-1
NM_173655 EPHA6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1825828 1.82E-07 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_173665 C5orf36 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs17376456 3.00E-15 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_173667 FLJ37543 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2030889 6.48E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_173667 FLJ37543 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6449558 7.12E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_173672 PPIL6 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs9487094 4.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_173683 XKR6 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs7819412 3.00E-08 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_173685 NSMCE2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7004739 2.14E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_173688 NKAIN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1455576 4.71E-05 NBL-GWAS version 2 dbGaP|2895
NM_173688 NKAIN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4134468 7.74E-05 NBL-GWAS version 2 dbGaP|2895
NM_173688 NKAIN3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs900493 6.94E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_173688 NKAIN3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483170 5.79E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_173688 NKAIN3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1483172 6.77E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_173699 MAGEB18 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs5944185 7.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_173717 ELAC2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3944086 6.41E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_173794 FUNDC1 18957941 http://www.ncbi.nlm.nih.gov/pubmed/18957941 Personality rs6610953 6.00E-06 Genome-wide association scan for five major dimensions of personality. NHGRI|-1
NM_173797 PAPD4 20673876 http://www.ncbi.nlm.nih.gov/pubmed/20673876 "Depressive Disorder, Major" rs7713917 1.00E-06 "Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression." NHGRI|-1
NM_173797 PAPD4 21700879 http://www.ncbi.nlm.nih.gov/pubmed/21700879 Adiponectin rs13358260 5.00E-06 Novel Locus FER Is Associated With Serum HMW Adiponectin Levels. NHGRI|-1
NM_173802 C12orf72 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs12579938 1.00E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_173808 NEGR1 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Tissue Plasminogen Activator rs10493485 2.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_173808 NEGR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12024388 7.62E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_173808 NEGR1 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs12141391 7.00E-06 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_173808 NEGR1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs988421 2.14E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_173808 NEGR1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs2568958 1.00E-11 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_173808 NEGR1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs2568958 2.00E-08 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_173824 C3orf38 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs2880961 2.00E-07 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_173841 IL1RN 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs6734238 2.00E-17 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_173842 IL1RN 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs6734238 2.00E-17 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_173843 IL1RN 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs6734238 2.00E-17 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_173847 SPACA3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9904938 7.03E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_173848 RALYL 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs7837606 1.08E-06 NBL-GWAS version 1 dbGaP|2845
NM_173848 RALYL 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1427065 2.79E-07 NBL-GWAS version 1 dbGaP|2845
NM_173848 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs6473383 2.29E-05 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_173848 RALYL 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs6473383 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_173848 RALYL 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs1375785 8.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_173848 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6473464 8.19E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_173848 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4524788 5.67E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_173848 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs7006609 6.24E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_173848 RALYL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs6980733 1.02E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_173848 RALYL 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs731956 4.54E-06 NBL-GWAS version 1 dbGaP|2845
NM_173851 SLC30A8 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs13266634 2.00E-14 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_173851 SLC30A8 17460697 http://www.ncbi.nlm.nih.gov/pubmed/17460697 "Diabetes Mellitus, Type 2" rs13266634 3.00E-06 A variant in CDKAL1 influences insulin response and risk of type 2 diabetes. NHGRI|-1
NM_173851 SLC30A8 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NM_173851 SLC30A8 17463246 http://www.ncbi.nlm.nih.gov/pubmed/17463246 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. NHGRI|-1
NM_173851 SLC30A8 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 "Diabetes Mellitus, Type 2" rs13266634 5.00E-08 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_173851 SLC30A8 17293876 http://www.ncbi.nlm.nih.gov/pubmed/17293876 "Diabetes Mellitus, Type 2" rs13266634 6.00E-08 A genome-wide association study identifies novel risk loci for type 2 diabetes. NHGRI|-1
NM_173851 SLC30A8 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 "Diabetes Mellitus, Type 2" rs13266634 7.00E-06 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_173851 SLC30A8 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 "Diabetes Mellitus, Type 2" rs13266634 8.00E-08 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_173851 SLC30A8 19096518 http://www.ncbi.nlm.nih.gov/pubmed/19096518 "Hemoglobin A, Glycosylated" rs13266634 5.00E-08 "Novel association of HK1 with glycated hemoglobin in a non-diabetic population: a genome-wide evaluation of 14,618 participants in the Women's Genome Health Study." NHGRI|-1
NM_173851 SLC30A8 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs3802177 1.00E-08 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_173851 SLC30A8 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs11558471 3.00E-11 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_173854 SLC41A1 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs823156 1.00E-07 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_173854 SLC41A1 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson Disease rs947211 2.00E-12 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_173860 HOXC12 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs1443512 6.00E-16 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_174855 IDH3B 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1810636 1.00E-10 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_174856 IDH3B 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs1810636 1.00E-10 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_174886 TGIF1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs431220 5.88E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_174896 C1orf162 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12740822 8.90E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_174900 ZFP42 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4862792 2.06E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_174900 ZFP42 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4862792 6.45E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_174900 ZFP42 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, LDL" rs1431005 2.00E-07 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_174900 ZFP42 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4632716 7.25E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_174911 FAM84B 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostatic Neoplasms rs1016343 1.00E-07 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_174911 FAM84B 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs1016343 4.00E-10 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_174911 FAM84B 21743057 http://www.ncbi.nlm.nih.gov/pubmed/21743057 Prostatic Neoplasms rs13252298 4.00E-06 Genome-wide association study identifies new prostate cancer susceptibility loci. NHGRI|-1
NM_174911 FAM84B 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs2954021 1.00E-07 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_174911 FAM84B 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Lipids rs2954026 8.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_174911 FAM84B 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs17321515 4.00E-17 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_174911 FAM84B 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs17321515 7.00E-13 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_174911 FAM84B 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs2954029 2.00E-11 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_174911 FAM84B 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs2954029 3.00E-19 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_174911 FAM84B 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs2954033 9.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NM_174911 FAM84B 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, LDL" rs6987702 3.00E-06 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_174911 FAM84B 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Cholesterol rs6987702 3.00E-09 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_174911 FAM84B 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs2954038 7.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_174911 FAM84B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7012891 8.45E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_174911 FAM84B 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs1551398 5.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_174917 ACSF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3743979 2.02E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_174924 PDILT 19430482 http://www.ncbi.nlm.nih.gov/pubmed/19430482 Creatinine rs12917707 5.00E-16 Multiple loci associated with indices of renal function and chronic kidney disease. NHGRI|-1
NM_174924 PDILT 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs12917707 1.00E-20 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_174924 PDILT 19430482 http://www.ncbi.nlm.nih.gov/pubmed/19430482 "Kidney Failure, Chronic" rs12917707 2.00E-12 Multiple loci associated with indices of renal function and chronic kidney disease. NHGRI|-1
NM_174927 SPATA19 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs4397868 3.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_174932 BPIL2 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Erythrocyte Indices rs9609565 4.00E-10 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_174936 PCSK9 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 "Cholesterol, LDL" rs11591147 2.00E-44 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_174936 PCSK9 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Cholesterol, LDL" rs11206510 1.00E-10 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_174936 PCSK9 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 "Cholesterol, LDL" rs11206510 4.00E-11 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_174936 PCSK9 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, LDL" rs11206510 4.00E-08 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_174936 PCSK9 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs11206510 9.00E-08 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_174936 PCSK9 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs11206510 1.00E-08 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_174937 TCERG1L 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs10741243 5.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_174937 TCERG1L 19786962 http://www.ncbi.nlm.nih.gov/pubmed/19786962 Speech Perception rs4751178 7.00E-06 First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. NHGRI|-1
NM_174937 TCERG1L 21160409 http://www.ncbi.nlm.nih.gov/pubmed/21160409 HIV-1 rs4751185 7.00E-06 Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population. NHGRI|-1
NM_174938 FRMD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10868025 1.79E-07 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NM_174938 FRMD3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10868025 6.46E-07 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_174978 C14orf39 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs2093210 6.00E-17 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_175038 CNTN1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Alkaline Phosphatase rs1880887 1.00E-10 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_175052 ST8SIA4 18846501 http://www.ncbi.nlm.nih.gov/pubmed/18846501 Conduct Disorder rs13188771 2.00E-06 Does parental expressed emotion moderate genetic effects in ADHD? An exploration using a genome wide association scan. NHGRI|-1
NM_175052 ST8SIA4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs6885006 9.61E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_175052 ST8SIA4 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs4702982 6.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_175056 ZPLD1 21490949 http://www.ncbi.nlm.nih.gov/pubmed/21490949 Type 2 diabetes rs2063640 3.00E-06 Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. NHGRI|-1
NM_175056 ZPLD1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs17842780 1.05E-06 NBL-GWAS version 1 dbGaP|2845
NM_175056 ZPLD1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs991258 5.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_175058 PLEKHA7 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs381815 2.00E-09 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_175058 PLEKHA7 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11024074 1.00E-06 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_175060 CLEC14A 18075462 http://www.ncbi.nlm.nih.gov/pubmed/18075462 Coronary Vasospasm rs10498345 9.00E-07 A novel genetic marker for coronary spasm in women from a genome-wide single nucleotide polymorphism analysis. NHGRI|-1
NM_175060 CLEC14A 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs11849174 5.39E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_175060 CLEC14A 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1449720 6.80E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_175061 JAZF1 18264096 http://www.ncbi.nlm.nih.gov/pubmed/18264096 Prostatic Neoplasms rs10486567 2.00E-06 Multiple loci identified in a genome-wide association study of prostate cancer. NHGRI|-1
NM_175061 JAZF1 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs864745 5.00E-14 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_175061 JAZF1 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs849141 3.00E-11 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_175061 JAZF1 18952825 http://www.ncbi.nlm.nih.gov/pubmed/18952825 Body Height rs1635852 9.00E-10 Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis. NHGRI|-1
NM_175061 JAZF1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs849134 3.00E-09 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_175069 APTX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10971259 1.34E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_175073 APTX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10971259 1.34E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_175075 C8orf42 21646302 http://www.ncbi.nlm.nih.gov/pubmed/21646302 Bilirubin rs17665859 5.00E-07 Mayo genome consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. NHGRI|-1
NM_175075 C8orf42 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1703940 1.12E-07 NBL-GWAS version 2 dbGaP|2895
NM_175085 GART 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8971 6.96E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_175085 GART 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2834232 6.96E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_175566 CNTN5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2726363 6.62E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_175566 CNTN5 17903304 http://www.ncbi.nlm.nih.gov/pubmed/17903304 Atrial Fibrillation rs10501920 9.00E-06 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. NHGRI|-1
NM_175566 CNTN5 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs952700 6.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_175566 CNTN5 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs11212364 3.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_175566 CNTN5 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1960997 9.62E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_175566 CNTN5 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs2405657 3.00E-06 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_175566 CNTN5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2155907 4.02E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_175566 CNTN5 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2509843 2.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_175566 CNTN5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2509843 4.70E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_175566 CNTN5 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs4237591 2.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_175605 IFT88 20713499 http://www.ncbi.nlm.nih.gov/pubmed/20713499 Depressive Disorder rs7326068 3.00E-06 "Cross-disorder genomewide analysis of schizophrenia, bipolar disorder, and depression." NHGRI|-1
NM_175607 CNTN4 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs2619566 7.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_175607 CNTN4 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs4370013 4.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_175610 TJP1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs1471225 8.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_175611 GRIK1 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs363512 4.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_175611 GRIK1 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs458685 6.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_175613 CNTN4 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs2619566 7.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_175613 CNTN4 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs4370013 4.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_175629 DNMT3A 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs13428812 9.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_175630 DNMT3A 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs13428812 9.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_175710 CR1L 21700265 http://www.ncbi.nlm.nih.gov/pubmed/21700265 Blood Sedimentation rs7527798 2.00E-09 Complement receptor 1 gene variants are associated with erythrocyte sedimentation rate. NHGRI|-1
NM_175710 CR1L 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs4844614 2.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_175710 CR1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs4844614 2.38E-07 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NM_175738 RAB37 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs10512597 8.00E-11 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_175747 OLIG3 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs2327832 4.00E-19 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_175747 OLIG3 17982456 http://www.ncbi.nlm.nih.gov/pubmed/17982456 "Arthritis, Rheumatoid" rs10499194 1.00E-09 Two independent alleles at 6q23 associated with risk of rheumatoid arthritis. NHGRI|-1
NM_175747 OLIG3 17982456 http://www.ncbi.nlm.nih.gov/pubmed/17982456 "Arthritis, Rheumatoid" rs6920220 1.00E-07 Two independent alleles at 6q23 associated with risk of rheumatoid arthritis. NHGRI|-1
NM_175747 OLIG3 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 "Arthritis, Rheumatoid" rs6920220 2.00E-09 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_175747 OLIG3 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs6920220 9.00E-13 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_175747 OLIG3 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6920220 8.00E-17 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_175768 GRIK2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1361168 7.90E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_175768 GRIK2 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Fibrinogen rs12207601 2.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_175768 GRIK2 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs4520040 3.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_175839 SMOX 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs16989303 6.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_175840 SMOX 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs16989303 6.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_175841 SMOX 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs16989303 6.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_175842 SMOX 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs16989303 6.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_175848 DNMT3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs437302 6.98E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_175849 DNMT3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs437302 6.98E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_175850 DNMT3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs437302 6.98E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_175858 KRTAP11-1 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs7283316 9.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_175882 IMP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12185268 1.90E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_175882 IMP5 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs12185268 3.00E-14 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_175882 IMP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12373139 4.91E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_175884 FLJ36031 19221038 http://www.ncbi.nlm.nih.gov/pubmed/19221038 Platelet Count rs342293 1.00E-24 "A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function." NHGRI|-1
NM_175884 FLJ36031 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Platelet Count rs342293 2.00E-33 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_175884 FLJ36031 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs17153527 4.00E-07 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_175886 PRPS1L1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs615545 5.89E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_175895 C12orf61 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs7302017 5.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_175910 ZNF493 19207018 http://www.ncbi.nlm.nih.gov/pubmed/19207018 Pain Measurement rs2562456 2.00E-10 Genome-wide association study of acute post-surgical pain in humans. NHGRI|-1
NM_175913 JPH2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs6073330 3.85E-05 NBL-GWAS version 2 dbGaP|2895
NM_175914 HNF4A 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs1800961 8.00E-10 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_175914 HNF4A 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs1800961 2.00E-09 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_175914 HNF4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs1800961 7.13E-07 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_175914 HNF4A 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6017342 1.00E-20 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_175914 HNF4A 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs6017342 9.00E-17 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_175922 PRR18 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs6915183 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_175924 ILDR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs11718322 8.23E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_175940 DUOX1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7169193 3.89E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_175940 DUOX1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1648312 3.44E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_176071 P2RY2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1783596 1.78E-06 NBL-GWAS version 1 dbGaP|2845
NM_176072 P2RY2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1783596 1.78E-06 NBL-GWAS version 1 dbGaP|2845
NM_176791 GTSF1L 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11696193 6.20E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_176810 NLRP13 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2117900 6.55E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_176817 TAS2R38 20675712 http://www.ncbi.nlm.nih.gov/pubmed/20675712 "Hemoglobin A, Glycosylated" rs713598 2.00E-104 The perception of quinine taste intensity is associated with common genetic variants in a bitter receptor cluster on chromosome 12. NHGRI|-1
NM_176876 P2RY12 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs7637803 6.71E-06 NBL-GWAS version 1 dbGaP|2845
NM_176891 IFNE 19578365 http://www.ncbi.nlm.nih.gov/pubmed/19578365 Dysplastic Nevus Syndrome rs4636294 3.00E-15 Genome-wide association study identifies variants at 9p21 and 22q13 associated with development of cutaneous nevi. NHGRI|-1
NM_177398 LMX1A 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs1532815 6.00E-07 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_177398 LMX1A 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs723821 1.42E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_177414 PPAP2B 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs17114036 4.00E-19 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_177414 PPAP2B 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs17114046 2.00E-07 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_177414 PPAP2B 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1930762 3.92E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_177435 PPARD 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs9658108 5.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_177435 PPARD 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs4713858 4.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_177438 DICER1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11624318 7.62E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_177438 DICER1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11160219 3.45E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_177438 DICER1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8007115 4.06E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_177438 DICER1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs8019257 8.50E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_177483 GPLD1 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs9467160 1.00E-11 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_177538 CYP20A1 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Height rs11888559 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_177540 TAS1R1 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Basophils rs11587438 4.00E-06 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_177553 GAS2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs7111546 2.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_177964 LYPD6B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs16822509 3.22E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_177964 LYPD6B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10201643 1.96E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_177964 LYPD6B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10929935 7.26E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_177964 LYPD6B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs10929935 5.43E-04 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_177965 C8orf37 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs3104917 2.52E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_177965 C8orf37 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6982567 2.33E-07 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_177965 C8orf37 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6982567 2.80E-07 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_177965 C8orf37 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs17668689 9.85E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_177990 PAK7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2423422 8.96E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_178006 STARD13 20364137 http://www.ncbi.nlm.nih.gov/pubmed/20364137 Intracranial Aneurysm rs9315204 3.00E-09 Genome-wide association study of intracranial aneurysm identifies three new risk loci. NHGRI|-1
NM_178007 STARD13 20364137 http://www.ncbi.nlm.nih.gov/pubmed/20364137 Intracranial Aneurysm rs9315204 3.00E-09 Genome-wide association study of intracranial aneurysm identifies three new risk loci. NHGRI|-1
NM_178009 DGKH 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs6561030 7.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_178009 DGKH 17486107 http://www.ncbi.nlm.nih.gov/pubmed/17486107 Bipolar Disorder rs1012053 2.00E-08 A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder. NHGRI|-1
NM_178009 DGKH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs1886811 2.38E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_178010 SOX5 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Triglycerides rs7979575 2.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_178010 SOX5 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs1464500 1.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_178010 SOX5 19754311 http://www.ncbi.nlm.nih.gov/pubmed/19754311 Acquired Immunodeficiency Syndrome rs1522232 2.00E-06 Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). NHGRI|-1
NM_178010 SOX5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs550338 8.88E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_178010 SOX5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11046688 4.39E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NM_178014 TUBB 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs3095329 3.00E-06 Genotype-Phenotype Associations in Multiple Sclerosis dbGaP|2861
NM_178130 TXNDC6 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs9846480 8.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_178138 LHX3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1747856 2.98E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_178140 PDZD2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4867365 1.62E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_178140 PDZD2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs16901423 1.23E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_178154 FUT8 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1256531 4.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_178155 FUT8 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1256531 4.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_178156 FUT8 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1256531 4.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_178157 FUT8 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1256531 4.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_178171 GSDMA 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs3894194 5.00E-09 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NM_178171 GSDMA 21150878 http://www.ncbi.nlm.nih.gov/pubmed/21150878 Asthma rs6503525 5.00E-07 "Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia." NHGRI|-1
NM_178171 GSDMA 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Leukocyte Count rs17609240 9.00E-09 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_178221 ATG4C 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs17124318 6.00E-07 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_178221 ATG4C 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Weight rs17124318 4.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_178221 ATG4C 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs10493340 2.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_178221 ATG4C 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs12130333 2.00E-08 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_178234 TUSC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6985300 4.38E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_178234 TUSC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1390052 8.02E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_178234 TUSC3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1390053 7.02E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_178237 EXOC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs4333263 1.12E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_178237 EXOC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs13120644 6.72E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_178313 SPTBN1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs11898505 2.00E-08 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_178313 SPTBN1 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone Density rs11898505 4.00E-06 New sequence variants associated with bone mineral density. NHGRI|-1
NM_178313 SPTBN1 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone Density rs11898505 8.00E-07 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_178313 SPTBN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6734445 4.13E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_178313 SPTBN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2941579 4.11E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_178324 SPTLC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs7023075 1.47E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_178328 CCR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9990343 2.76E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_178328 CCR3 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs9990343 4.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_178328 CCR3 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs6441961 3.00E-07 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_178329 CCR3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9990343 2.76E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_178329 CCR3 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs9990343 4.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_178329 CCR3 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac Disease rs6441961 3.00E-07 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_178423 HDAC9 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs615545 5.89E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_178425 HDAC9 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs615545 5.89E-06 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_178432 CDK20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10868677 8.79E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_178435 LCE3E 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs10888501 1.00E-06 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_178435 LCE3E 19169255 http://www.ncbi.nlm.nih.gov/pubmed/19169255 Psoriasis rs4085613 7.00E-30 Psoriasis genome-wide association study identifies susceptibility variants within LCE gene cluster at 1q21. NHGRI|-1
NM_178435 LCE3E 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs4112788 3.00E-10 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_178435 LCE3E 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair rs499697 1.00E-10 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_178438 LCE5A 19896111 http://www.ncbi.nlm.nih.gov/pubmed/19896111 Hair rs908922 4.00E-06 Common variants in the trichohyalin gene are associated with straight hair in Europeans. NHGRI|-1
NM_178456 C20orf85 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1334109 9.09E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_178457 ZNF831 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Myopia rs12625057 7.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_178457 ZNF831 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs6070744 1.20E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_178457 ZNF831 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs16982520 2.00E-07 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_178483 C20orf79 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs7272481 4.99E-08 NBL-GWAS version 1 dbGaP|2845
NM_178496 C3orf59 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4455277 1.94E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_178496 C3orf59 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3952738 1.94E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_178496 C3orf59 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7643379 5.25E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_178498 SLC5A12 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4431984 4.62E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_178499 CCDC60 18332876 http://www.ncbi.nlm.nih.gov/pubmed/18332876 Schizophrenia rs11064768 1.00E-06 A genome-wide association study in 574 schizophrenia trios using DNA pooling. NHGRI|-1
NM_178499 CCDC60 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Exercise Test rs7137869 6.00E-07 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_178499 CCDC60 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1918416 4.88E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_178509 STXBP4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1156287 5.28E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_178509 STXBP4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs9303363 9.25E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_178516 EXOC3L 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs3729639 2.00E-11 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_178527 SLC9A11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6684491 1.38E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_178527 SLC9A11 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6678784 4.80E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_178549 ZNF678 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs1390401 5.00E-09 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_178550 C1orf110 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2343331 2.46E-06 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_178550 C1orf110 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2343278 9.28E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_178550 C1orf110 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2841974 4.67E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_178550 C1orf110 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2841979 9.97E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_178559 ABCB5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2709748 1.38E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_178559 ABCB5 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs10950821 7.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_178565 RSPO2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs7818981 9.90E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_178565 RSPO2 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain rs4534106 1.00E-06 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_178566 ZDHHC21 19754311 http://www.ncbi.nlm.nih.gov/pubmed/19754311 Acquired Immunodeficiency Syndrome rs1556032 9.00E-06 Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). NHGRI|-1
NM_178566 ZDHHC21 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs303746 9.39E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_178569 C5orf38 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs10042985 8.53E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_178578 PSMF1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6040222 7.79E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_178586 PPP2R5C 20663923 http://www.ncbi.nlm.nih.gov/pubmed/20663923 Autistic Disorder rs7142002 3.00E-06 A genome-wide scan for common alleles affecting risk for autism. NHGRI|-1
NM_178587 PPP2R5C 20663923 http://www.ncbi.nlm.nih.gov/pubmed/20663923 Autistic Disorder rs7142002 3.00E-06 A genome-wide scan for common alleles affecting risk for autism. NHGRI|-1
NM_178815 ARL5B 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10829156 4.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_178820 FBXO27 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs930100 2.15E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_178821 WDR69 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs10200894 1.90E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_178839 LRRTM1 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Menopause rs10496265 1.00E-08 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_178839 LRRTM1 17903295 http://www.ncbi.nlm.nih.gov/pubmed/17903295 Menopause rs10496262 3.00E-07 Genetic correlates of longevity and selected age-related phenotypes: a genome-wide association study in the Framingham Study. NHGRI|-1
NM_178839 LRRTM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Blood Pressure rs7570909 9.77E-05 Genomewide association analysis of systolic blood pressure (SBP) in a birth cohort from a founder population dbGaP|2903
NM_178839 LRRTM1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1237758 2.17E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_178839 LRRTM1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2568112 2.17E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_178839 LRRTM1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1432170 1.79E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_178839 LRRTM1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs4852655 1.88E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_178839 LRRTM1 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Stomach Neoplasms rs17022444 1.00E-10 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_178849 HNF4A 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs1800961 8.00E-10 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_178849 HNF4A 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs1800961 2.00E-09 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_178849 HNF4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs1800961 7.13E-07 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_178849 HNF4A 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6017342 1.00E-20 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_178849 HNF4A 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs6017342 9.00E-17 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_178850 HNF4A 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs1800961 8.00E-10 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_178850 HNF4A 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs1800961 2.00E-09 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_178850 HNF4A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, HDL" rs1800961 7.13E-07 Genomewide association analysis of high density lipoproteins (HDL) in a birth cohort from a founder population dbGaP|2900
NM_178850 HNF4A 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6017342 1.00E-20 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_178850 HNF4A 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs6017342 9.00E-17 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_178864 NPAS4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs7935572 1.99E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_178868 CMTM8 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs4380451 4.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_181042 PBRM1 20081856 http://www.ncbi.nlm.nih.gov/pubmed/20081856 Mood Disorders rs2251219 2.00E-09 Meta-analysis of genome-wide association data identifies a risk locus for major mood disorders on 3p21.1. NHGRI|-1
NM_181050 AXIN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11644916 6.24E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_181050 AXIN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11648673 4.77E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_181054 HIF1A 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 CD40 Ligand rs8005745 4.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_181078 IL21R 19874204 http://www.ncbi.nlm.nih.gov/pubmed/19874204 Bone Density rs8057551 2.00E-06 IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study. NHGRI|-1
NM_181079 IL21R 19874204 http://www.ncbi.nlm.nih.gov/pubmed/19874204 Bone Density rs8057551 2.00E-06 IL21R and PTH may underlie variation of femoral neck bone mineral density as revealed by a genome-wide association study. NHGRI|-1
NM_181309 IL22RA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4896243 2.67E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_181310 IL22RA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4896243 2.67E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_181332 NLGN4X 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Fibrinogen rs7885458 3.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_181332 NLGN4X 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic Lateral Sclerosis rs5916687 3.00E-06 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_181349 SMURF1 20228798 http://www.ncbi.nlm.nih.gov/pubmed/20228798 "Colitis, Ulcerative" rs7809799 9.00E-11 Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). NHGRI|-1
NM_181351 NCAM1 21212386 http://www.ncbi.nlm.nih.gov/pubmed/21212386 Blood Vessels rs1436109 3.00E-07 Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. NHGRI|-1
NM_181351 NCAM1 21212386 http://www.ncbi.nlm.nih.gov/pubmed/21212386 Blood Vessels rs1436109 4.00E-09 Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. NHGRI|-1
NM_181351 NCAM1 21212386 http://www.ncbi.nlm.nih.gov/pubmed/21212386 Blood Vessels rs1436109 9.00E-07 Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families. NHGRI|-1
NM_181351 NCAM1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs12279261 9.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_181351 NCAM1 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs7105881 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_181356 SUPT3H 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs3799977 5.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_181356 SUPT3H 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs10948197 8.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_181356 SUPT3H 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs9395066 8.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_181359 IL6R 19567438 http://www.ncbi.nlm.nih.gov/pubmed/19567438 C-Reactive Protein rs4537545 2.00E-14 Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease. NHGRI|-1
NM_181359 IL6R 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs4129267 2.00E-48 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_181359 IL6R 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Maximal Midexpiratory Flow Rate rs4129267 7.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_181359 IL6R 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 "Receptors, Interleukin-6" rs4129267 2.00E-57 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_181359 IL6R 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs2228145 2.00E-08 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_181359 IL6R 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs2228145 2.00E-11 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_181361 KCNMB2 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs9290663 6.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_181361 KCNMB2 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs12629106 4.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_181361 KCNMB2 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs644695 5.00E-06 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_181361 KCNMB2 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs7612209 4.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_181361 KCNMB2 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs1982821 4.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_181435 C1QTNF3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10075914 7.33E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_181435 C1QTNF3 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs409045 8.00E-07 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NM_181446 FSHR 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs2268363 5.00E-08 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_181446 FSHR 19165918 http://www.ncbi.nlm.nih.gov/pubmed/19165918 "Lupus Erythematosus, Systemic" rs17039212 9.00E-06 Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. NHGRI|-1
NM_181446 FSHR 20923822 http://www.ncbi.nlm.nih.gov/pubmed/20923822 Response to radiation rs7591064 5.00E-06 Radiation pharmacogenomics: a genome-wide association approach to identify radiation response biomarkers using human lymphoblastoid cell lines. NHGRI|-1
NM_181457 PAX3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs348970 1.96E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_181458 PAX3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs348970 1.96E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_181459 PAX3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs348970 1.96E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_181460 PAX3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs348970 1.96E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_181461 PAX3 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs348970 1.96E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_181466 EIF6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs619865 5.21E-04 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_181466 EIF6 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Melanosis rs619865 5.00E-14 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_181468 EIF6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs619865 5.21E-04 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_181468 EIF6 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Melanosis rs619865 5.00E-14 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_181472 CMTM7 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs12638540 3.00E-07 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_181481 C18orf1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6505798 8.21E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_181482 C18orf1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6505798 8.21E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_181483 C18orf1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs6505798 8.21E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_181485 ZGPAT 18758464 http://www.ncbi.nlm.nih.gov/pubmed/18758464 Inflammatory Bowel Diseases rs2315008 9.00E-15 Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. NHGRI|-1
NM_181485 ZGPAT 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs4809330 3.00E-15 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_181486 TBX5 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs883079 1.00E-10 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_181486 TBX5 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3825214 1.00E-07 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_181486 TBX5 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3825214 3.00E-12 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_181486 TBX5 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs3825214 3.00E-13 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_181486 TBX5 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1946295 7.87E-06 NBL-GWAS version 1 dbGaP|2845
NM_181493 ITPA 20637204 http://www.ncbi.nlm.nih.gov/pubmed/20637204 Anemia rs1127354 4.00E-44 ITPA polymorphism affects ribavirin-induced anemia and outcomes of therapy--a genome-wide study of Japanese HCV virus patients. NHGRI|-1
NM_181493 ITPA 21659334 http://www.ncbi.nlm.nih.gov/pubmed/21659334 "Hepatitis C, Chronic" rs6139030 1.00E-15 Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C. NHGRI|-1
NM_181493 ITPA 21659334 http://www.ncbi.nlm.nih.gov/pubmed/21659334 "Hepatitis C, Chronic" rs6139030 2.00E-25 Genome-wide association study identified ITPA/DDRGK1 variants reflecting thrombocytopenia in pegylated interferon and ribavirin therapy for chronic hepatitis C. NHGRI|-1
NM_181500 CUX1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2906724 3.94E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_181500 CUX1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11974778 8.09E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_181501 ITGA1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2447859 7.32E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_181501 ITGA1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2456206 7.03E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_181507 HPS5 21124955 http://www.ncbi.nlm.nih.gov/pubmed/21124955 Serum Amyloid A Protein rs4353250 2.00E-51 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. NHGRI|-1
NM_181508 HPS5 21124955 http://www.ncbi.nlm.nih.gov/pubmed/21124955 Serum Amyloid A Protein rs4353250 2.00E-51 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. NHGRI|-1
NM_181552 CUX1 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2906724 3.94E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_181552 CUX1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs11974778 8.09E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_181558 RFC3 19749422 http://www.ncbi.nlm.nih.gov/pubmed/19749422 Alzheimer Disease rs690705 6.00E-07 Genome-Wide Scan of Copy Number Variation in Late-Onset Alzheimer's Disease. NHGRI|-1
NM_181571 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_181571 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_181571 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_181571 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_181571 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_181573 RFC4 20011104 http://www.ncbi.nlm.nih.gov/pubmed/20011104 Adiponectin rs266717 9.00E-19 A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. NHGRI|-1
NM_181573 RFC4 20011104 http://www.ncbi.nlm.nih.gov/pubmed/20011104 Adiponectin rs1648707 3.00E-12 A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. NHGRI|-1
NM_181573 RFC4 20876611 http://www.ncbi.nlm.nih.gov/pubmed/20876611 Adiponectin rs864265 1.00E-19 Genome-wide association study for adiponectin levels in Filipino women identifies CDH13 and a novel uncommon haplotype at KNG1-ADIPOQ. NHGRI|-1
NM_181578 RFC5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs7295696 1.77E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_181581 DUS4L 21068099 http://www.ncbi.nlm.nih.gov/pubmed/21068099 "Osteoarthritis, Knee" rs4730250 6.00E-08 Meta-analysis of genome-wide association studies confirms a susceptibility locus for knee osteoarthritis on chromosome 7q22. NHGRI|-1
NM_181598 ATL1 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs17122693 3.00E-07 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_181646 ZNF804B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs1406503 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_181646 ZNF804B 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs6959888 2.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NM_181651 PRDX5 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs694739 4.00E-07 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_181651 PRDX5 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs694739 6.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_181652 PRDX5 20596022 http://www.ncbi.nlm.nih.gov/pubmed/20596022 Alopecia Areata rs694739 4.00E-07 Genome-wide association study in alopecia areata implicates both innate and adaptive immunity. NHGRI|-1
NM_181652 PRDX5 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs694739 6.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_181654 CPLX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs12232751 1.20E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_181654 CPLX4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs9973180 9.04E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_181659 NCOA3 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs6125048 2.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NM_181661 VPS13B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4735627 2.26E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_181670 ANKS1B 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Benzodiazepines rs7968606 3.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NM_181670 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Body Mass Index rs2373011 9.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_181670 ANKS1B 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Waist Circumference rs2373011 2.00E-06 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_181670 ANKS1B 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 "Memory, Short-Term" rs11110077 4.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_181671 PITPNC1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2537828 3.82E-06 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_181674 PPP2R2B 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs1864982 3.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_181674 PPP2R2B 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs9325032 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_181675 PPP2R2B 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs1864982 3.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_181675 PPP2R2B 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs9325032 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_181676 PPP2R2B 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs1864982 3.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_181676 PPP2R2B 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs9325032 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_181677 PPP2R2B 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs1864982 3.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_181677 PPP2R2B 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs9325032 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_181678 PPP2R2B 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcoholism rs1864982 3.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_181678 PPP2R2B 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs9325032 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_181690 AKT3 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs4132509 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_181690 AKT3 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs10927101 2.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_181690 AKT3 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs476141 1.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_181690 AKT3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1000543 1.25E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_181690 AKT3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2454222 6.14E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_181690 AKT3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2454221 8.28E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_181690 AKT3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2047137 9.15E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_181698 CCNY 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs12261843 7.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_181698 CCNY 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12261843 4.05E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_181701 QSOX2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs7849585 5.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_181701 QSOX2 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs12338076 2.00E-08 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_181707 C17orf64 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs8071181 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_181708 BCDIN3D 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Mass Index rs7138803 1.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_181708 BCDIN3D 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body Mass Index rs7138803 2.00E-17 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_181708 BCDIN3D 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body Weight rs7138803 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_181708 BCDIN3D 19557197 http://www.ncbi.nlm.nih.gov/pubmed/19557197 Waist Circumference rs7138803 8.00E-07 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. NHGRI|-1
NM_181709 FAM101A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs4765078 1.67E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_181714 LCA5 21190210 http://www.ncbi.nlm.nih.gov/pubmed/21190210 Obsessive-Compulsive Disorder rs3747767 7.00E-07 Genome-wide association study of hoarding traits. NHGRI|-1
NM_181719 TMCO4 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs16822732 5.30E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_181719 TMCO4 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs3748748 6.63E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_181723 EFHA2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs10090288 3.27E-06 NBL-GWAS version 1 dbGaP|2845
NM_181733 COG5 20112360 http://www.ncbi.nlm.nih.gov/pubmed/20112360 Osteoarthritis rs3815148 8.00E-08 A genome-wide association study identifies an osteoarthritis susceptibility locus on chromosome 7q22. NHGRI|-1
NM_181746 LASS2 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs267734 1.00E-12 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_181775 PLXNA4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3734991 1.62E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_181775 PLXNA4 17903300 http://www.ncbi.nlm.nih.gov/pubmed/17903300 Body Mass Index rs1106683 1.00E-07 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. NHGRI|-1
NM_181775 PLXNA4 17903300 http://www.ncbi.nlm.nih.gov/pubmed/17903300 Body Mass Index rs1106684 2.00E-06 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. NHGRI|-1
NM_181780 BTLA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2633580 3.66E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_181780 BTLA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs2633578 3.53E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_181784 SPRED2 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs934734 5.00E-10 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_181784 SPRED2 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs1876518 2.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_181785 SLC46A3 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1305088 9.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_181791 GPR141 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2722292 5.10E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_181791 GPR141 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2597279 8.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_181798 KCNQ1 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs2074238 3.00E-17 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_181798 KCNQ1 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs12296050 3.00E-17 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_181798 KCNQ1 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs12296050 8.00E-11 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_181798 KCNQ1 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12576239 1.00E-15 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_181798 KCNQ1 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs179429 7.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_181798 KCNQ1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs231362 3.00E-13 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_181798 KCNQ1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 L-Lactate Dehydrogenase rs2237878 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_181798 KCNQ1 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 "Diabetes Mellitus, Type 2" rs2237892 1.00E-26 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_181798 KCNQ1 18711367 http://www.ncbi.nlm.nih.gov/pubmed/18711367 "Diabetes Mellitus, Type 2" rs2237892 2.00E-42 Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus. NHGRI|-1
NM_181798 KCNQ1 21573907 http://www.ncbi.nlm.nih.gov/pubmed/21573907 "Diabetes Mellitus, Type 2" rs2237892 4.00E-06 "Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas." NHGRI|-1
NM_181798 KCNQ1 20174558 http://www.ncbi.nlm.nih.gov/pubmed/20174558 "Diabetes Mellitus, Type 2" rs2237895 1.00E-09 A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. NHGRI|-1
NM_181798 KCNQ1 18711366 http://www.ncbi.nlm.nih.gov/pubmed/18711366 "Diabetes Mellitus, Type 2" rs2237897 1.00E-16 SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations. NHGRI|-1
NM_181807 DCDC1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone Density rs16921914 2.00E-09 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_181839 PKIA 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs7821178 3.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_181839 PKIA 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs7846385 5.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_181839 PKIA 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs3864663 2.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_181839 PKIA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs10091852 8.64E-05 NBL-GWAS version 2 dbGaP|2895
NM_181842 ZBTB12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs558702 1.60E-86 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NM_181842 ZBTB12 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs558702 2.89E-18 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NM_181842 ZBTB12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs558702 4.20E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_181842 ZBTB12 21105107 http://www.ncbi.nlm.nih.gov/pubmed/21105107 "Carcinoma, Hepatocellular" rs9267673 2.00E-06 Genetic variations at loci involved in the immune response are risk factors for hepatocellular carcinoma. NHGRI|-1
NM_181842 ZBTB12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9267673 2.30E-33 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_181842 ZBTB12 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs644045 2.06E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_181842 ZBTB12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs511294 1.45E-13 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_181842 ZBTB12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs511294 6.27E-13 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_181842 ZBTB12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs544167 2.48E-13 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_181842 ZBTB12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs544167 7.79E-13 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_181872 DMRT2 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs17641078 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_181874 GRM7 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs3749380 2.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_181874 GRM7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs10510351 3.30E-04 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_181874 GRM7 21368711 http://www.ncbi.nlm.nih.gov/pubmed/21368711 Personality rs13080594 8.00E-07 Genome-wide association study of personality traits in bipolar patients. NHGRI|-1
NM_181874 GRM7 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 "Depressive Disorder, Major" rs9870680 1.00E-06 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_181874 GRM7 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Factor VII rs4591494 9.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_181897 PPP2R3A 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs823968 6.68E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_182485 CPEB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs16889099 1.85E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_182485 CPEB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2270279 8.13E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_182485 CPEB2 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Count rs10489087 5.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_182485 CPEB2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1013284 4.93E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_182486 C1QTNF6 20410501 http://www.ncbi.nlm.nih.gov/pubmed/20410501 Vitiligo rs229527 2.00E-16 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. NHGRI|-1
NM_182486 C1QTNF6 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs229541 2.00E-07 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_182486 C1QTNF6 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 "Diabetes Mellitus, Type 1" rs229541 2.00E-08 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_182486 C1QTNF6 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Arthritis, Rheumatoid" rs743777 1.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_182486 C1QTNF6 21653640 http://www.ncbi.nlm.nih.gov/pubmed/21653640 "Arthritis, Rheumatoid" rs743777 2.00E-06 Pathway-driven gene stability selection of two rheumatoid arthritis GWAS identifies and validates new susceptibility genes in receptor mediated signalling pathways. NHGRI|-1
NM_182486 C1QTNF6 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs229492 7.75E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_182495 FAM55B 17903292 http://www.ncbi.nlm.nih.gov/pubmed/17903292 Albumins rs1712790 2.00E-06 A genome-wide association for kidney function and endocrine-related traits in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_182503 ADAT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2496585 1.21E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_182508 C13orf30 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1325803 1.57E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_182511 CBLN2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs8092443 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_182511 CBLN2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Risperidone rs11663206 2.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_182511 CBLN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1395851 4.64E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_182511 CBLN2 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs2660917 8.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_182511 CBLN2 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs17083844 6.00E-06 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_182511 CBLN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs9953717 7.66E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_182511 CBLN2 19656524 http://www.ncbi.nlm.nih.gov/pubmed/19656524 Cleft Lip rs17085106 4.00E-08 A genome-wide association study identifies a locus for nonsyndromic cleft lip with or without cleft palate on 8q24. NHGRI|-1
NM_182511 CBLN2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs337718 9.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_182523 CMC1 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs12632457 1.90E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_182536 GKN2 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs4254535 5.00E-06 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_182551 LCLAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs829642 4.80E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_182551 LCLAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs829646 6.34E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_182552 WDR27 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs3734905 2.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_182560 C14orf177 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs4900384 4.00E-09 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_182560 C14orf177 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Platelet Aggregation rs10484128 6.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_182560 C14orf177 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Amyotrophic Lateral Sclerosis rs1459148 2.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NM_182562 FAM169B 20634892 http://www.ncbi.nlm.nih.gov/pubmed/20634892 Neurotic Disorders rs4965121 1.00E-06 A genome-wide association study of neuroticism in a population-based sample. NHGRI|-1
NM_182562 FAM169B 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11856483 4.54E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_182574 MAMSTR 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs281379 7.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_182595 POM121L12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs17578222 3.30E-05 NBL-GWAS version 2 dbGaP|2895
NM_182595 POM121L12 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema rs1012036 5.00E-06 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_182595 POM121L12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs10266118 2.46E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_182608 ANKRD33 21107309 http://www.ncbi.nlm.nih.gov/pubmed/21107309 Intuition rs17126180 9.00E-07 Genome-wide pharmacogenomic study of neurocognition as an indicator of antipsychotic treatment response in schizophrenia. NHGRI|-1
NM_182616 C15orf38 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Personality rs7178909 5.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_182623 FAM131C 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs9442235 6.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_182640 MRPS9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs7584136 7.13E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_182640 MRPS9 17668382 http://www.ncbi.nlm.nih.gov/pubmed/17668382 "Diabetes Mellitus, Type 2" rs6712932 6.00E-06 Type 2 diabetes whole-genome association study in four populations: the DiaGen consortium. NHGRI|-1
NM_182644 EPHA3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs9832305 6.12E-06 NBL-GWAS version 1 dbGaP|2845
NM_182644 EPHA3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs6782527 9.75E-07 NBL-GWAS version 1 dbGaP|2845
NM_182644 EPHA3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs6774870 3.32E-06 NBL-GWAS version 1 dbGaP|2845
NM_182644 EPHA3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs907548 5.53E-06 NBL-GWAS version 1 dbGaP|2845
NM_182644 EPHA3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1915304 3.23E-06 NBL-GWAS version 1 dbGaP|2845
NM_182644 EPHA3 21177773 http://www.ncbi.nlm.nih.gov/pubmed/21177773 Acetaminophen rs2880961 2.00E-07 Acetaminophen-NAPQI hepatotoxicity: a cell line model system genome-wide association study. NHGRI|-1
NM_182646 CPEB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs16889099 1.85E-04 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_182646 CPEB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs2270279 8.13E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_182646 CPEB2 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Count rs10489087 5.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_182646 CPEB2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1013284 4.93E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_182678 UBE2E3 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs13010713 5.00E-11 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_182678 UBE2E3 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs1018326 2.00E-06 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_182678 UBE2E3 21041692 http://www.ncbi.nlm.nih.gov/pubmed/21041692 Heart Function Tests rs7602460 6.00E-06 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. NHGRI|-1
NM_182687 PKMYT1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs886427 6.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_182699 DDX53 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs5925696 3.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_182700 SP8 20386566 http://www.ncbi.nlm.nih.gov/pubmed/20386566 Bipolar Disorder rs2709736 5.00E-07 Genome-wide association study of bipolar I disorder in the Han Chinese population. NHGRI|-1
NM_182700 SP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2709748 1.38E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_182717 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182717 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182717 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182717 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182717 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182718 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182718 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182718 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182718 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182718 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182719 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182719 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182719 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182719 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182719 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182720 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182720 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182720 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182720 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182720 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182721 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182721 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182721 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182721 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182721 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182722 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182722 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182722 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182722 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182722 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182723 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182723 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182723 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182723 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182723 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182724 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182724 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182724 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182724 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182724 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182725 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182725 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182725 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182725 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182725 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182734 PLCB1 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs6056209 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_182749 N6AMT1 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs2832077 2.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_182755 ZNF438 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_182755 ZNF438 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11008171 7.96E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_182757 RNF144B 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs41441749 1.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_182758 WDR72 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs7168365 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_182758 WDR72 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Creatinine rs10518733 2.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_182758 WDR72 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Creatinine rs491567 3.00E-13 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_182758 WDR72 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs12595250 5.56E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_182758 WDR72 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs493218 5.38E-07 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_182758 WDR72 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs689771 2.28E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_182758 WDR72 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs518127 2.29E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_182758 WDR72 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs572221 6.69E-07 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_182758 WDR72 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs690271 5.07E-07 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_182758 WDR72 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs566369 5.07E-07 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_182758 WDR72 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs482541 5.07E-07 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_182758 WDR72 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4109297 8.28E-06 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_182759 FAM19A3 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs11590090 3.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_182760 SUMF1 20802204 http://www.ncbi.nlm.nih.gov/pubmed/20802204 Multiple Sclerosis rs794185 6.00E-07 Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. NHGRI|-1
NM_182761 FAM170A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs184497 6.86E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_182762 MACC1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs38152 7.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_182767 SLC6A15 20662065 http://www.ncbi.nlm.nih.gov/pubmed/20662065 Lupus Vulgaris rs2403106 3.00E-06 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. NHGRI|-1
NM_182767 SLC6A15 21521612 http://www.ncbi.nlm.nih.gov/pubmed/21521612 "Depressive Disorder, Major" rs1545843 1.00E-09 The neuronal transporter gene SLC6A15 confers risk to major depression. NHGRI|-1
NM_182767 SLC6A15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs2125716 1.13E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_182769 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182769 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182769 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182769 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182769 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182770 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182770 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182770 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182770 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182770 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182771 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182771 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182771 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182771 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182771 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182772 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182772 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182772 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182772 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182772 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182775 ALS2CL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs7633016 3.19E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_182775 ALS2CL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4076927 2.53E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_182796 MAT2B 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs6556756 5.00E-07 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_182796 MAT2B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2964318 3.61E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_182797 PLCB4 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs6039424 9.55E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_182797 PLCB4 20172861 http://www.ncbi.nlm.nih.gov/pubmed/20172861 Leukocyte Count rs2072910 3.00E-10 Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count. NHGRI|-1
NM_182798 EGFLAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs2956597 9.25E-06 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_182798 EGFLAM 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs270545 1.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_182799 EGFLAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs2956597 9.25E-06 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_182799 EGFLAM 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs270545 1.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_182801 EGFLAM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs2956597 9.25E-06 Genome-wide association between genotype and incident heart failure in participants of primarily self-described European ancestry dbGaP|2884
NM_182801 EGFLAM 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs270545 1.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_182802 MCM8 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause rs236114 1.00E-10 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_182802 MCM8 20205591 http://www.ncbi.nlm.nih.gov/pubmed/20205591 HIV-1 rs454422 1.00E-06 Host determinants of HIV-1 control in African Americans. NHGRI|-1
NM_182802 MCM8 19448621 http://www.ncbi.nlm.nih.gov/pubmed/19448621 Menarche rs16991615 1.00E-21 Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. NHGRI|-1
NM_182826 SCARA3 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs569214 4.00E-08 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_182830 MDGA2 18762592 http://www.ncbi.nlm.nih.gov/pubmed/18762592 Neurotic Disorders rs12883384 7.00E-07 Genomewide association analysis followed by a replication study implicates a novel candidate gene for neuroticism. NHGRI|-1
NM_182830 MDGA2 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Blood Viscosity rs7159841 2.00E-07 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_182848 CLDN10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs870707 2.95E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NM_182850 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182850 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182850 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182850 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182850 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182853 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182853 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182853 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182853 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182853 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_182854 SNX20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs9302752 1.45E-12 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_182854 SNX20 20018961 http://www.ncbi.nlm.nih.gov/pubmed/20018961 Leprosy rs9302752 4.00E-40 Genomewide association study of leprosy. NHGRI|-1
NM_182854 SNX20 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs7194886 1.41E-07 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_182854 SNX20 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs7194886 2.42E-07 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_182898 CREB5 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs11765845 7.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_182898 CREB5 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2237349 5.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_182899 CREB5 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs11765845 7.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_182899 CREB5 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs2237349 5.00E-06 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_182907 PRDM1 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs548234 5.00E-12 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_182907 PRDM1 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs9386463 6.00E-07 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_182907 PRDM1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs7746082 2.00E-10 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_182907 PRDM1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs6911490 1.00E-08 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_182910 SYNE2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7229 5.64E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_182913 SYNE2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7229 5.64E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_182914 SYNE2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7229 5.64E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_182918 ERG 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs7275212 2.00E-18 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NM_182918 ERG 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2836496 7.04E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_182918 ERG 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2836505 5.78E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_182918 ERG 20662065 http://www.ncbi.nlm.nih.gov/pubmed/20662065 Lupus Vulgaris rs743446 5.00E-06 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. NHGRI|-1
NM_182920 ADAMTS9 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-Hip Ratio rs6795735 2.00E-16 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_182920 ADAMTS9 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs4607103 1.00E-08 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_182920 ADAMTS9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs10510933 3.46E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_182920 ADAMTS9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4688187 1.93E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_182925 FLT4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2387207 4.50E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_182932 SLC8A3 21602797 http://www.ncbi.nlm.nih.gov/pubmed/21602797 Cystic Fibrosis rs12883884 8.00E-06 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. NHGRI|-1
NM_182935 MOBP 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs1768208 5.00E-17 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NM_182935 MOBP 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs816488 4.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_182935 MOBP 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs864643 1.00E-08 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_182936 SLC8A3 21602797 http://www.ncbi.nlm.nih.gov/pubmed/21602797 Cystic Fibrosis rs12883884 8.00E-06 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. NHGRI|-1
NM_182948 PRKACB 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs1085093 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_182961 SYNE1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs2673776 8.05E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_182961 SYNE1 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs17082664 1.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_182961 SYNE1 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs17082664 4.00E-06 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_182961 SYNE1 21738484 http://www.ncbi.nlm.nih.gov/pubmed/21738484 Bipolar Disorder rs7747960 9.00E-06 Genome-Wide Association of Bipolar Disorder Suggests an Enrichment of Replicable Associations in Regions near Genes. NHGRI|-1
NM_182961 SYNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2623963 7.61E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_182961 SYNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs7745725 1.87E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_182961 SYNE1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1358317 1.61E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_182961 SYNE1 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood Pressure rs1322512 8.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_182964 NAV2 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs874426 4.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_182966 NEDD9 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11751998 6.75E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_182972 IRF2BP2 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs744487 5.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_182974 GLT6D1 19897590 http://www.ncbi.nlm.nih.gov/pubmed/19897590 Periodontitis rs1537415 6.00E-09 A genome-wide association study identifies GLT6D1 as a susceptibility locus for periodontitis. NHGRI|-1
NM_182975 ZNF326 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs2136093 4.00E-07 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_182975 ZNF326 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Atherosclerosis rs2390582 1.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_182975 ZNF326 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12116456 8.28E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_182975 ZNF326 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17131133 5.10E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_182975 ZNF326 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12133004 2.75E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_182976 ZNF326 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs2136093 4.00E-07 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_182976 ZNF326 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Atherosclerosis rs2390582 1.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_182976 ZNF326 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12116456 8.28E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_182976 ZNF326 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs17131133 5.10E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_182976 ZNF326 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12133004 2.75E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_182978 GNAL 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10468679 1.72E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183002 SLC8A3 21602797 http://www.ncbi.nlm.nih.gov/pubmed/21602797 Cystic Fibrosis rs12883884 8.00E-06 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. NHGRI|-1
NM_183011 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183011 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183011 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183011 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183011 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183012 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183012 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183012 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183012 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183012 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183013 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183013 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183013 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183013 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183013 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183040 DTNBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs9296985 1.07E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_183043 RNF6 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs9512144 6.15E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183044 RNF6 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs9512144 6.15E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183047 ZMYND8 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs11696358 9.43E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_183048 ZMYND8 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs11696358 9.43E-06 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4437429 1.00E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4437429 4.34E-06 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9448894 7.14E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9448894 7.28E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4706113 7.14E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4706113 7.28E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2322631 4.13E-06 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2322631 9.67E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10080237 4.13E-06 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10080237 9.67E-06 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs978814 1.91E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs978814 3.03E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3812121 2.07E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3812121 4.03E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2179842 2.61E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2179842 3.51E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9352817 8.23E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs9352817 8.91E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7453746 7.12E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_183050 BCKDHB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7453746 7.86E-06 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_183058 LYZL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11008171 7.96E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_183058 LYZL2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs3124177 2.70E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_183058 LYZL2 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10763807 1.45E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183059 RD3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10863899 1.67E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183060 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs10827492 1.69E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183060 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934540 1.83E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183060 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11593858 2.14E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183060 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12768019 2.31E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183060 CREM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4934724 3.21E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_183079 PRNP 19081515 http://www.ncbi.nlm.nih.gov/pubmed/19081515 Creutzfeldt-Jakob Syndrome rs1799990 2.00E-21 Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. NHGRI|-1
NM_183079 PRNP 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet Aggregation rs6052699 2.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_183228 IKZF3 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs907092 8.00E-06 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_183228 IKZF3 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs9303277 2.00E-09 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_183229 IKZF3 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs907092 8.00E-06 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_183229 IKZF3 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs9303277 2.00E-09 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_183230 IKZF3 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs907092 8.00E-06 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_183230 IKZF3 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs9303277 2.00E-09 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_183231 IKZF3 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs907092 8.00E-06 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_183231 IKZF3 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs9303277 2.00E-09 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_183232 IKZF3 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs907092 8.00E-06 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_183232 IKZF3 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs9303277 2.00E-09 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NM_183233 SLC22A18 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs16928809 1.00E-07 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_183357 ADCY5 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs11708067 7.00E-22 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_183357 ADCY5 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs11708067 3.00E-12 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_183357 ADCY5 20081857 http://www.ncbi.nlm.nih.gov/pubmed/20081857 Glucose Tolerance Test rs2877716 7.00E-16 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. NHGRI|-1
NM_183357 ADCY5 20372150 http://www.ncbi.nlm.nih.gov/pubmed/20372150 Birth Weight rs9883204 7.00E-15 Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight. NHGRI|-1
NM_183360 DTNB 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11684202 6.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_183361 DTNB 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11684202 6.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_183376 ARRDC4 20634892 http://www.ncbi.nlm.nih.gov/pubmed/20634892 Neurotic Disorders rs4965121 1.00E-06 A genome-wide association study of neuroticism in a population-based sample. NHGRI|-1
NM_183376 ARRDC4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11856483 4.54E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_183376 ARRDC4 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2045325 9.57E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_183377 ACCN1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs11650066 6.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_183393 CADPS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs304230 1.40E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_183394 CADPS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs304230 1.40E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_183395 NLRP3 20031576 http://www.ncbi.nlm.nih.gov/pubmed/20031576 Fibrinogen rs1539019 1.00E-08 Association of novel genetic Loci with circulating fibrinogen levels: a genome-wide association study in 6 population-based cohorts. NHGRI|-1
NM_183395 NLRP3 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs12239046 1.00E-15 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_183395 NLRP3 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs10399826 2.06E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183395 NLRP3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs11802371 1.11E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_183398 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs252139 7.04E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183398 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs252095 4.58E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183398 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs409037 4.58E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183399 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs252139 7.04E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183399 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs252095 4.58E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183399 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs409037 4.58E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183400 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs252139 7.04E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183400 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs252095 4.58E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183400 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs409037 4.58E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183401 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs252139 7.04E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183401 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs252095 4.58E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183401 RNF14 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs409037 4.58E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_183415 UBE3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7298565 6.93E-05 NBL-GWAS version 2 dbGaP|2895
NM_183415 UBE3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs7486178 3.90E-06 NBL-GWAS version 2 dbGaP|2895
NM_183416 KIF1B 18997785 http://www.ncbi.nlm.nih.gov/pubmed/18997785 Multiple Sclerosis rs10492972 3.00E-10 Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis. NHGRI|-1
NM_183416 KIF1B 20676096 http://www.ncbi.nlm.nih.gov/pubmed/20676096 "Carcinoma, Hepatocellular" rs17401966 2.00E-18 Genome-wide association study identifies 1p36.22 as a new susceptibility locus for hepatocellular carcinoma in chronic hepatitis B virus carriers. NHGRI|-1
NM_183419 RNF19A 21041692 http://www.ncbi.nlm.nih.gov/pubmed/21041692 Heart Function Tests rs1371867 9.00E-06 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. NHGRI|-1
NM_183425 RBM38 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs6092477 1.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_183425 RBM38 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs6070116 4.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_194247 HNRNPA3 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1529093 2.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_194250 ZNF804A 18677311 http://www.ncbi.nlm.nih.gov/pubmed/18677311 Schizophrenia rs1344706 2.00E-07 Identification of loci associated with schizophrenia by genome-wide association and follow-up. NHGRI|-1
NM_194255 SLC19A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9976523 7.46E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_194255 SLC19A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs9980967 2.07E-04 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_194255 SLC19A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11701130 2.79E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_194255 SLC19A1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs4819143 7.47E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_194285 SPTY2D1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10500833 3.49E-04 Genome-wide association between genotype and incident stroke in participants of primarily self-described European ancestry dbGaP|2886
NM_194287 C14orf166B 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7160583 2.54E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_194291 TMEM65 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10808533 3.05E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_194298 SLC16A9 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Uric Acid rs12356193 1.00E-08 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_194314 ZBTB41 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12137359 2.05E-13 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_194314 ZBTB41 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12137359 2.68E-12 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_194314 ZBTB41 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4520444 3.64E-11 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_194314 ZBTB41 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4520444 8.05E-12 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_194314 ZBTB41 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6656448 5.63E-06 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_194314 ZBTB41 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6656448 8.77E-09 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_194314 ZBTB41 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6690022 5.06E-05 "Genome-Wide Genotypic Association of AMD Status in Illumina Human-1 (100k) Chip (Pre-computed)" dbGaP|2856
NM_194314 ZBTB41 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1764629 5.01E-06 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_194318 B3GALTL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9315120 6.90E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_194429 FGFR1OP 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2301436 1.00E-12 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_194429 FGFR1OP 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs2301436 6.00E-08 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_194434 VAPA 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7228911 6.74E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_194434 VAPA 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs7228911 9.02E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_194435 VIP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs546599 2.19E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_194435 VIP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs633596 5.06E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_194439 RNF212 18239089 http://www.ncbi.nlm.nih.gov/pubmed/18239089 "Recombination, Genetic" rs1670533 2.00E-12 Sequence variants in the RNF212 gene associate with genome-wide recombination rate. NHGRI|-1
NM_194439 RNF212 18239089 http://www.ncbi.nlm.nih.gov/pubmed/18239089 "Recombination, Genetic" rs3796619 3.00E-24 Sequence variants in the RNF212 gene associate with genome-wide recombination rate. NHGRI|-1
NM_194439 RNF212 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6839931 2.09E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_194439 RNF212 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs7669622 4.53E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_194439 RNF212 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6827357 5.15E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_197957 MAX 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Erythrocyte Indices rs4466998 5.00E-08 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_197957 MAX 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Waist Circumference rs7158173 4.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_197970 BOLL 18997786 http://www.ncbi.nlm.nih.gov/pubmed/18997786 Intracranial Aneurysm rs700651 4.00E-08 Susceptibility loci for intracranial aneurysm in European and Japanese populations. NHGRI|-1
NM_197972 NME7 21502573 http://www.ncbi.nlm.nih.gov/pubmed/21502573 D-dimer levels rs16861990 2.00E-06 Genetic predictors of fibrin D-dimer levels in healthy adults. NHGRI|-1
NM_197978 HEMGN 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Thyrotropin rs755109 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_197978 HEMGN 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Artery Disease rs4743150 5.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_198053 CD247 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs840016 2.00E-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_198053 CD247 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs864537 2.00E-11 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_198053 CD247 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs864537 4.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_198053 CD247 20383147 http://www.ncbi.nlm.nih.gov/pubmed/20383147 "Scleroderma, Systemic" rs2056626 3.00E-09 Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. NHGRI|-1
NM_198053 CD247 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs2056626 1.00E-06 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NM_198056 SCN5A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs11129795 5.00E-10 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_198056 SCN5A 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs11129795 5.00E-14 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_198056 SCN5A 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs12053903 1.00E-14 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_198056 SCN5A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs12053903 1.00E-07 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_198056 SCN5A 19389651 http://www.ncbi.nlm.nih.gov/pubmed/19389651 Electrocardiography rs7638909 2.00E-06 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. NHGRI|-1
NM_198056 SCN5A 21347284 http://www.ncbi.nlm.nih.gov/pubmed/21347284 Electrocardiography rs3922844 3.00E-23 Genome-wide association studies of the PR interval in African Americans. NHGRI|-1
NM_198056 SCN5A 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 Electrocardiography rs11708996 6.00E-26 Genome-wide association study of PR interval. NHGRI|-1
NM_198056 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11708996 7.00E-06 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_198056 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11710077 1.00E-06 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_198056 SCN5A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9851724 6.00E-16 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_198074 OR2C3 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 "Leukemia, Lymphoid" rs1881797 7.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_198076 FAM36A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11801533 5.61E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_198080 MSRB3 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs10506525 6.00E-09 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_198080 MSRB3 20195514 http://www.ncbi.nlm.nih.gov/pubmed/20195514 Odontogenesis rs10506525 9.00E-07 Genome-wide association study reveals multiple loci associated with primary tooth development during infancy. NHGRI|-1
NM_198080 MSRB3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10784460 2.18E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_198080 MSRB3 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic Nephropathies rs2358944 4.00E-06 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_198137 CATSPER4 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs11809207 6.00E-08 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_198152 UTS2D 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs10937470 9.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_198155 C21orf33 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2838519 6.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_198155 C21orf33 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs762421 1.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_198158 MITF 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs922948 2.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_198159 MITF 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs922948 2.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_198173 GRHL3 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs4649203 7.00E-08 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_198174 GRHL3 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs4649203 7.00E-08 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_198177 MITF 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs922948 2.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_198178 MITF 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs922948 2.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_198185 OVCH2 19557197 http://www.ncbi.nlm.nih.gov/pubmed/19557197 Waist Circumference rs7932813 5.00E-06 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. NHGRI|-1
NM_198186 ASTN2 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs10983238 1.00E-07 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_198186 ASTN2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs3761845 8.63E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_198186 ASTN2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10817974 1.11E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_198186 ASTN2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs4838255 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_198186 ASTN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs17302884 5.16E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_198187 ASTN2 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs10983238 1.00E-07 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_198187 ASTN2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs3761845 8.63E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_198187 ASTN2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10817974 1.11E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_198187 ASTN2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs4838255 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_198187 ASTN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs17302884 5.16E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_198188 ASTN2 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs10983238 1.00E-07 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NM_198188 ASTN2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs3761845 8.63E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_198188 ASTN2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10817974 1.11E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_198188 ASTN2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Perphenazine rs4838255 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_198188 ASTN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs17302884 5.16E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_198196 CD96 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs76884941 1.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_198196 CD96 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs56238310 1.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NM_198212 CAV2 20835238 http://www.ncbi.nlm.nih.gov/pubmed/20835238 "Glaucoma, Open-Angle" rs4236601 2.00E-11 Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma. NHGRI|-1
NM_198213 OASL 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs7957197 2.00E-08 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_198215 FAM13C 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs10509101 3.95E-05 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NM_198220 SNRPB2 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs3787509 9.03E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_198253 TERT 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Count rs2736100 3.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_198253 TERT 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs2736100 1.00E-14 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_198253 TERT 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs2736100 2.00E-17 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_198253 TERT 18835860 http://www.ncbi.nlm.nih.gov/pubmed/18835860 Idiopathic Pulmonary Fibrosis rs2736100 3.00E-08 A genome-wide association study identifies an association of a common variant in TERT with susceptibility to idiopathic pulmonary fibrosis. NHGRI|-1
NM_198253 TERT 21725308 http://www.ncbi.nlm.nih.gov/pubmed/21725308 Lung Neoplasms rs2736100 1.00E-27 A genome-wide association study identifies 2 new lung cancer susceptibility loci at 13q12.12 and 22q12.2 in Han Chinese NHGRI|-1
NM_198253 TERT 19836008 http://www.ncbi.nlm.nih.gov/pubmed/19836008 Lung Neoplasms rs2736100 2.00E-10 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. NHGRI|-1
NM_198253 TERT 20700438 http://www.ncbi.nlm.nih.gov/pubmed/20700438 Lung Neoplasms rs2736100 2.00E-22 The 5p15.33 locus is associated with risk of lung adenocarcinoma in never-smoking females in Asia. NHGRI|-1
NM_198253 TERT 20871597 http://www.ncbi.nlm.nih.gov/pubmed/20871597 Lung Neoplasms rs2736100 3.00E-11 Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations. NHGRI|-1
NM_198253 TERT 20543847 http://www.ncbi.nlm.nih.gov/pubmed/20543847 Testicular Neoplasms rs2736100 8.00E-15 "Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer." NHGRI|-1
NM_198253 TERT 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs2853676 4.00E-14 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_198253 TERT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4635969 1.05E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_198253 TERT 20543847 http://www.ncbi.nlm.nih.gov/pubmed/20543847 Testicular Neoplasms rs4635969 1.00E-23 "Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer." NHGRI|-1
NM_198253 TERT 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs4975616 3.00E-09 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_198253 TERT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4975616 8.29E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_198256 E2F6 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs6716724 6.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_198276 TMEM17 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 "Spondylitis, Ankylosing" rs10865331 2.00E-19 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_198276 TMEM17 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs10865331 7.00E-34 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_198281 GPRIN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4106153 9.18E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_198281 GPRIN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs1504489 8.42E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_198281 GPRIN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs12644119 2.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_198281 GPRIN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356229 5.48E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_198281 GPRIN3 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs356219 2.00E-47 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_198281 GPRIN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11931074 4.78E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_198281 GPRIN3 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson Disease rs11931074 7.00E-17 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_198281 GPRIN3 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs356220 2.00E-19 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_198281 GPRIN3 20711177 http://www.ncbi.nlm.nih.gov/pubmed/20711177 Parkinson Disease rs356220 3.00E-11 Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. NHGRI|-1
NM_198281 GPRIN3 21084426 http://www.ncbi.nlm.nih.gov/pubmed/21084426 Parkinson Disease rs356220 3.00E-08 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. NHGRI|-1
NM_198281 GPRIN3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs356220 6.99E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_198281 GPRIN3 21044948 http://www.ncbi.nlm.nih.gov/pubmed/21044948 Parkinson Disease rs356220 9.00E-16 Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. NHGRI|-1
NM_198285 WDR86 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs13232179 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_198315 VWA5A 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs880321 7.55E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_198321 GALNT10 21701570 http://www.ncbi.nlm.nih.gov/pubmed/21701570 Body Mass Index rs2033195 6.00E-06 Genome-Wide Association of BMI in African Americans. NHGRI|-1
NM_198332 STAT2 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs2066808 1.00E-09 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NM_198332 STAT2 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs2066808 2.00E-07 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_198332 STAT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11575221 5.71E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_198381 ELF5 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs1323690 1.74E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_198381 ELF5 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Brain rs5028798 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_198392 TCF21 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs12190287 1.00E-12 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_198400 NEDD4 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs8032158 6.00E-13 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_198401 ANKRD46 21041692 http://www.ncbi.nlm.nih.gov/pubmed/21041692 Heart Function Tests rs1371867 9.00E-06 Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science. NHGRI|-1
NM_198407 GHSR 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs572169 3.00E-18 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_198427 BCAN 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs11360 3.57E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_198441 PRR20A 20833655 http://www.ncbi.nlm.nih.gov/pubmed/20833655 Warfarin rs1512651 6.00E-06 Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. NHGRI|-1
NM_198449 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2036902 9.88E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198449 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13157992 9.03E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198449 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7720960 7.28E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198449 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7378969 6.04E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198449 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1016620 9.80E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198449 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs559096 9.08E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198449 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1674512 9.15E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198449 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4865676 9.06E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198449 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10064702 9.15E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198449 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7710841 9.06E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198449 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10042504 9.15E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198461 LONRF2 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs11676922 1.00E-14 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_198461 LONRF2 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs9653442 5.00E-06 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_198461 LONRF2 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs10865035 2.00E-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_198463 C3orf67 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs2121794 2.14E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_198464 PRSS55 20452100 http://www.ncbi.nlm.nih.gov/pubmed/20452100 Neurofibrillary Tangles rs11782819 3.00E-06 Alzheimer disease pathology in cognitively healthy elderly: A genome-wide study. NHGRI|-1
NM_198467 RSBN1L 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Creatinine rs6465825 2.00E-09 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_198468 C6orf167 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Thyrotropin rs6909430 8.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_198468 C6orf167 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs9491640 9.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_198480 ZNF615 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11878803 1.07E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_198491 FAM92B 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs8050910 2.00E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_198493 ANKRD45 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12065033 3.39E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_198493 ANKRD45 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs6678784 4.80E-06 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7529369 5.67E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs12407399 5.19E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7554267 7.80E-13 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7554267 7.93E-12 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10494742 4.52E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2027368 1.54E-23 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2027368 5.66E-24 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7535696 2.97E-24 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7535696 8.60E-25 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs16839884 1.57E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs16839884 2.58E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs16839886 4.01E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs16839886 7.26E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3927686 1.85E-24 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3927686 4.28E-25 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs16839906 5.33E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801533 1.21E-11 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801533 4.39E-11 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2878557 5.19E-24 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs2878557 5.80E-25 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10494743 2.15E-11 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10494743 6.58E-12 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801538 2.02E-11 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10801538 6.25E-12 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1339951 4.86E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10754192 4.96E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10494744 1.35E-11 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10494744 4.40E-12 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4294368 5.30E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10754196 2.45E-26 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10754196 4.44E-27 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_198503 KCNT2 20662065 http://www.ncbi.nlm.nih.gov/pubmed/20662065 Lupus Vulgaris rs1890645 4.00E-06 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. NHGRI|-1
NM_198503 KCNT2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs10494737 4.69E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_198503 KCNT2 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs7517337 2.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10922013 4.23E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_198503 KCNT2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs7512769 2.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_198503 KCNT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs7535849 2.36E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_198506 LRIT3 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 Exercise Test rs6847149 3.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_198507 FAM174A 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs4702982 6.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_198507 FAM174A 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Erythrocyte Indices rs1829883 6.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_198507 FAM174A 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs10067427 5.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_198521 C12orf42 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs10745954 2.00E-11 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_198521 C12orf42 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-Reactive Protein rs10778213 1.00E-10 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_198545 C1orf187 18347602 http://www.ncbi.nlm.nih.gov/pubmed/18347602 Schizophrenia rs4846033 4.00E-06 Genomewide association for schizophrenia in the CATIE study: results of stage 1. NHGRI|-1
NM_198551 MIA3 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs17465637 1.00E-08 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_198551 MIA3 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs17465637 1.00E-06 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_198551 MIA3 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs17465637 1.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_198552 FAM89A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4388693 3.06E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_198567 C5orf25 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13169783 3.54E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198567 C5orf25 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11134972 1.63E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198567 C5orf25 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs11134973 2.29E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NM_198569 GPR126 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs6570507 2.00E-07 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_198569 GPR126 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs6570507 4.00E-11 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_198569 GPR126 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs4896582 2.00E-18 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_198569 GPR126 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs3817928 1.00E-09 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_198569 GPR126 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs3748069 5.00E-14 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_198569 GPR126 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs9496398 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_198569 GPR126 21060863 http://www.ncbi.nlm.nih.gov/pubmed/21060863 Retinal Vein rs225717 1.00E-16 "Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo." NHGRI|-1
NM_198570 VWC2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs7796855 7.32E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_198576 AGRN 19851299 http://www.ncbi.nlm.nih.gov/pubmed/19851299 Body Mass Index rs3934834 6.00E-07 Linkage and genome-wide association analysis of obesity-related phenotypes: association of weight with the MGAT1 gene. NHGRI|-1
NM_198578 LRRK2 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs1491942 6.00E-14 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_198578 LRRK2 21738487 http://www.ncbi.nlm.nih.gov/pubmed/21738487 Parkinson Disease rs34637584 2.00E-28 Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease. NHGRI|-1
NM_198578 LRRK2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs11175593 3.00E-10 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_198580 SLC27A1 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs11666579 3.00E-06 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_198596 SULF2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4810663 1.93E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_198596 SULF2 18937294 http://www.ncbi.nlm.nih.gov/pubmed/18937294 Attention Deficit Disorder with Hyperactivity rs4810685 7.00E-06 Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder. NHGRI|-1
NM_198596 SULF2 20173747 http://www.ncbi.nlm.nih.gov/pubmed/20173747 Atrial Fibrillation rs13038095 2.00E-07 Common variants in KCNN3 are associated with lone atrial fibrillation. NHGRI|-1
NM_198709 ARSB 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs337847 7.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_198709 ARSB 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs2052550 8.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_198714 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_198714 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 8.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_198714 PTGER3 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs10458561 4.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NM_198715 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_198715 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 8.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_198715 PTGER3 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs10458561 4.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NM_198716 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_198716 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 8.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_198716 PTGER3 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs10458561 4.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NM_198717 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_198717 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 8.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_198717 PTGER3 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs10458561 4.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NM_198718 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_198718 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 8.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_198718 PTGER3 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs10458561 4.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NM_198719 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_198719 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 8.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_198719 PTGER3 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs10458561 4.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NM_198721 COL25A1 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs4956211 1.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_198827 GPR133 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs3847687 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_198827 GPR133 19729412 http://www.ncbi.nlm.nih.gov/pubmed/19729412 Body Height rs1569019 5.00E-08 Genetic variation in GPR133 is associated with height: genome wide association study in the self-contained population of Sorbs. NHGRI|-1
NM_198827 GPR133 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs885389 4.00E-08 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_198827 GPR133 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs7299940 7.00E-06 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_198828 MAST4 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs1030231 9.35E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NM_198828 MAST4 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Nonalcoholic Fatty Liver Disease rs1697137 2.00E-06 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_198828 MAST4 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs10514995 1.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NM_198828 MAST4 20595579 http://www.ncbi.nlm.nih.gov/pubmed/20595579 Longevity rs10069397 5.00E-08 Genetic signatures of exceptional longevity in humans. NHGRI|-1
NM_198844 ZPBP2 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs2872507 9.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_198844 ZPBP2 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2872507 5.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_198844 ZPBP2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2872507 5.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_198844 ZPBP2 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs8067378 1.00E-07 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_198859 PRICKLE2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs152296 5.15E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_198859 PRICKLE2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4688187 1.93E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_198859 PRICKLE2 19303062 http://www.ncbi.nlm.nih.gov/pubmed/19303062 Folic Acid rs153734 7.00E-06 "Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations." NHGRI|-1
NM_198890 ATG16L1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs10210302 5.00E-14 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_198890 ATG16L1 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs3828309 2.00E-32 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_198890 ATG16L1 17435756 http://www.ncbi.nlm.nih.gov/pubmed/17435756 Crohn Disease rs2241880 1.00E-13 Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. NHGRI|-1
NM_198890 ATG16L1 20570966 http://www.ncbi.nlm.nih.gov/pubmed/20570966 Crohn Disease rs2241880 3.00E-06 Fucosyltransferase 2 (FUT2) non-secretor status is associated with Crohn's disease. NHGRI|-1
NM_198890 ATG16L1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2241880 4.40E-08 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_198890 ATG16L1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs3792109 7.00E-41 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_198890 ATG16L1 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs3792106 2.31E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_198890 ATG16L1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs10933436 7.00E-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_198920 UBE2CBP 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2917494 5.90E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_198951 TGM2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6023059 6.26E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_198955 MGAT5B 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs9916886 4.52E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_198956 SP8 20386566 http://www.ncbi.nlm.nih.gov/pubmed/20386566 Bipolar Disorder rs2709736 5.00E-07 Genome-wide association study of bipolar I disorder in the Han Chinese population. NHGRI|-1
NM_198956 SP8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2709748 1.38E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_198964 PTHLH 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs522958 1.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_198964 PTHLH 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs522958 8.00E-07 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_198964 PTHLH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7137085 3.38E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_198965 PTHLH 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs522958 1.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_198965 PTHLH 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs522958 8.00E-07 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_198965 PTHLH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7137085 3.38E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_198966 PTHLH 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs522958 1.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_198966 PTHLH 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs522958 8.00E-07 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_198966 PTHLH 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7137085 3.38E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NM_198989 DLEU7 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs2408213 5.24E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_198989 DLEU7 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs1262778 8.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_198989 DLEU7 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs1239947 8.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_198989 DLEU7 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs3116602 7.00E-09 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_198989 DLEU7 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs3118914 4.00E-10 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_198990 NAPEPLD 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1968199 1.46E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_198991 KCTD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Attention Deficit Disorder with Hyperactivity rs6508445 7.37E-05 " TDT test of genome-wide association on ADHD trios (Pre-computed)" dbGaP|2875
NM_198991 KCTD1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs16942421 8.00E-10 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_198992 SYT10 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs11052413 1.18E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_198992 SYT10 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs12424662 1.14E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NM_198995 C18orf34 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9956150 5.48E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_198998 AQP12A 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4456706 2.60E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_199000 LHFPL3 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs10953454 7.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_199040 NUDT4 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1836127 3.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_199043 C14orf102 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2282032 1.19E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_199043 C14orf102 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs2282032 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_199051 FAM5C 17903301 http://www.ncbi.nlm.nih.gov/pubmed/17903301 Heart Atria rs1935881 6.00E-06 "Genome-wide association of echocardiographic dimensions, brachial artery endothelial function and treadmill exercise responses in the Framingham Heart Study." NHGRI|-1
NM_199051 FAM5C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs2490271 1.88E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_199051 FAM5C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1327872 3.15E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_199051 FAM5C 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs17379742 7.67E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_199051 FAM5C 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs2053302 4.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_199051 FAM5C 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn Disease rs10801047 3.00E-08 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_199051 FAM5C 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs10737562 7.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_199051 FAM5C 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 "Carotid Artery, Common" rs1400544 6.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_199076 CNNM2 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs12413409 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_199076 CNNM2 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Disease rs12413409 4.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_199076 CNNM2 20364137 http://www.ncbi.nlm.nih.gov/pubmed/20364137 Intracranial Aneurysm rs12413409 1.00E-09 Genome-wide association study of intracranial aneurysm identifies three new risk loci. NHGRI|-1
NM_199077 CNNM2 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs12413409 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_199077 CNNM2 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary Disease rs12413409 4.00E-06 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_199077 CNNM2 20364137 http://www.ncbi.nlm.nih.gov/pubmed/20364137 Intracranial Aneurysm rs12413409 1.00E-09 Genome-wide association study of intracranial aneurysm identifies three new risk loci. NHGRI|-1
NM_199078 CNNM3 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs9948 6.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NM_199131 VAX1 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Cleft Lip rs7078160 2.00E-08 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_199133 FAM173B 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs6884905 9.18E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_199161 SAA1 21124955 http://www.ncbi.nlm.nih.gov/pubmed/21124955 Serum Amyloid A Protein rs4638289 3.00E-53 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. NHGRI|-1
NM_199168 CXCL12 17634449 http://www.ncbi.nlm.nih.gov/pubmed/17634449 Coronary Disease rs501120 9.00E-08 Genomewide association analysis of coronary artery disease. NHGRI|-1
NM_199168 CXCL12 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs1746048 3.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_199168 CXCL12 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial Infarction rs1746048 7.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_199169 PMEPA1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1334109 9.09E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_199170 PMEPA1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1334109 9.09E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_199171 PMEPA1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1334109 9.09E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NM_199186 BPGM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12539126 8.96E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_199186 BPGM 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10488456 6.08E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_199191 BRE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs10189899 5.82E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_199192 BRE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs10189899 5.82E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_199193 BRE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs10189899 5.82E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_199194 BRE 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs10189899 5.82E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_199206 TCL1B 20876420 http://www.ncbi.nlm.nih.gov/pubmed/20876420 Aromatase Inhibitors rs7158782 8.00E-07 Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors. NHGRI|-1
NM_199231 GDNF 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs270545 1.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_199245 VAMP1 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs10492096 3.00E-06 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_199246 CCNG1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs17061327 6.05E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_199280 FAM179A 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 "Depressive Disorder, Major" rs882632 2.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_199292 TH 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs7111341 4.00E-48 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_199292 TH 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs7127900 3.00E-33 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_199293 TH 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs7111341 4.00E-48 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_199293 TH 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs7127900 3.00E-33 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_199321 ZPBP2 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs2872507 9.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_199321 ZPBP2 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2872507 5.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_199321 ZPBP2 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs2872507 5.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_199321 ZPBP2 20228799 http://www.ncbi.nlm.nih.gov/pubmed/20228799 "Colitis, Ulcerative" rs8067378 1.00E-07 Genome-wide association identifies multiple ulcerative colitis susceptibility loci. NHGRI|-1
NM_199355 ADAMTS18 19249006 http://www.ncbi.nlm.nih.gov/pubmed/19249006 Bone Density rs11864477 2.00E-08 Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups. NHGRI|-1
NM_199367 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4785684 2.98E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_199367 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3922634 2.73E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_199367 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3922633 2.73E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_199367 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs8052076 2.18E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_199367 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4785686 4.74E-06 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_199367 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11862081 5.40E-06 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_199367 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3803680 1.16E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_199367 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3803676 6.47E-06 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_199367 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs463701 6.36E-06 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_199367 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs382745 1.04E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_199367 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2056309 5.13E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_199367 SPG7 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs457372 8.13E-06 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NM_199413 PRC1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs8042680 2.00E-10 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_199414 PRC1 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 "Diabetes Mellitus, Type 2" rs8042680 2.00E-10 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_199426 ZFP64 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs6013382 5.00E-06 Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_199426 ZFP64 19478329 http://www.ncbi.nlm.nih.gov/pubmed/19478329 "Infertility, Male" rs6068020 5.00E-07 Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. NHGRI|-1
NM_199427 ZFP64 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs6013382 5.00E-06 Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data. NHGRI|-1
NM_199427 ZFP64 19478329 http://www.ncbi.nlm.nih.gov/pubmed/19478329 "Infertility, Male" rs6068020 5.00E-07 Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. NHGRI|-1
NM_199450 ZNF365 21278746 http://www.ncbi.nlm.nih.gov/pubmed/21278746 Breast Neoplasms rs10995190 1.00E-09 Common variants in ZNF365 are associated with both mammographic density and breast cancer risk. NHGRI|-1
NM_199450 ZNF365 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs10995190 5.00E-15 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_199450 ZNF365 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs10995271 4.00E-20 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_199450 ZNF365 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs10761659 2.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_199450 ZNF365 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs10761659 4.00E-22 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_199450 ZNF365 17435756 http://www.ncbi.nlm.nih.gov/pubmed/17435756 Crohn Disease rs224136 1.00E-10 Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. NHGRI|-1
NM_199450 ZNF365 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs224136 1.23E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_199451 ZNF365 21278746 http://www.ncbi.nlm.nih.gov/pubmed/21278746 Breast Neoplasms rs10995190 1.00E-09 Common variants in ZNF365 are associated with both mammographic density and breast cancer risk. NHGRI|-1
NM_199451 ZNF365 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs10995190 5.00E-15 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_199451 ZNF365 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs10995271 4.00E-20 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_199451 ZNF365 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs10761659 2.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_199451 ZNF365 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs10761659 4.00E-22 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_199451 ZNF365 17435756 http://www.ncbi.nlm.nih.gov/pubmed/17435756 Crohn Disease rs224136 1.00E-10 Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. NHGRI|-1
NM_199451 ZNF365 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs224136 1.23E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_199452 ZNF365 21278746 http://www.ncbi.nlm.nih.gov/pubmed/21278746 Breast Neoplasms rs10995190 1.00E-09 Common variants in ZNF365 are associated with both mammographic density and breast cancer risk. NHGRI|-1
NM_199452 ZNF365 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast Neoplasms rs10995190 5.00E-15 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_199452 ZNF365 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs10995271 4.00E-20 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_199452 ZNF365 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn Disease rs10761659 2.00E-06 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_199452 ZNF365 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs10761659 4.00E-22 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_199452 ZNF365 17435756 http://www.ncbi.nlm.nih.gov/pubmed/17435756 Crohn Disease rs224136 1.00E-10 Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. NHGRI|-1
NM_199452 ZNF365 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs224136 1.23E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_199453 HTR4 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Respiratory Function Tests rs11168048 1.00E-11 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_199453 HTR4 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Respiratory Function Tests rs3995090 4.00E-09 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_199454 PRDM16 21666692 http://www.ncbi.nlm.nih.gov/pubmed/21666692 Migraine Disorders rs2651899 4.00E-09 Genome-wide association study reveals three susceptibility loci for common migraine in the general population. NHGRI|-1
NM_199454 PRDM16 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2651916 1.93E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_199454 PRDM16 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10737190 2.04E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_199454 PRDM16 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Cholesterol rs6658356 2.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_199459 C10orf71 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs4838508 2.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_199487 UQCC 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs6060369 1.00E-16 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NM_199487 UQCC 18193045 http://www.ncbi.nlm.nih.gov/pubmed/18193045 Body Height rs6060369 2.00E-16 Common variants in the GDF5-UQCC region are associated with variation in human height. NHGRI|-1
NM_199487 UQCC 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs6088792 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_199487 UQCC 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs6060373 2.00E-17 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_199487 UQCC 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs6088813 1.00E-13 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_201253 CRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10754220 2.85E-10 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NM_201253 CRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs10754220 4.20E-11 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_201253 CRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1415214 9.74E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_201253 CRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs949571 3.31E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NM_201253 CRB1 20032318 http://www.ncbi.nlm.nih.gov/pubmed/20032318 Asthma rs2786098 2.00E-13 Variants of DENND1B associated with asthma in children. NHGRI|-1
NM_201253 CRB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1764629 5.01E-06 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_201264 NRP2 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs7603514 8.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_201266 NRP2 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs7603514 8.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_201267 NRP2 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs7603514 8.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_201274 MPRIP 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs11867934 7.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_201279 NRP2 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity rs7603514 8.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_201282 EGFR 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs11979158 7.00E-08 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_201282 EGFR 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs2252586 8.00E-08 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_201283 EGFR 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs11979158 7.00E-08 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_201283 EGFR 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs2252586 8.00E-08 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_201284 EGFR 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs11979158 7.00E-08 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_201284 EGFR 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs2252586 8.00E-08 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_201348 PRELP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6428009 6.92E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_201435 CCDC62 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs12817488 3.00E-13 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_201437 TCEA1 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs6473902 4.29E-05 Genomewide Association in Population-Based Samples dbGaP|2851
NM_201441 TEAD4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10774085 3.51E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_201443 TEAD4 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10774085 3.51E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_201532 DGKZ 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11038871 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_201533 DGKZ 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11038871 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_201546 CDCP2 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs682705 2.20E-05 Tier2b Allelic Association of Parkinson's Disease Using the Combined Samples from Tier1 and Tier2a dbGaP|2842
NM_201548 CERKL 18521091 http://www.ncbi.nlm.nih.gov/pubmed/18521091 Isoxazoles rs993648 3.00E-06 Whole genome association study identifies polymorphisms associated with QT prolongation during iloperidone treatment of schizophrenia. NHGRI|-1
NM_201551 NELL1 17684544 http://www.ncbi.nlm.nih.gov/pubmed/17684544 Crohn Disease rs1793004 3.00E-06 Systematic association mapping identifies NELL1 as a novel IBD disease gene. NHGRI|-1
NM_201551 NELL1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs1987307 5.86E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NM_201551 NELL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Iron rs1670646 9.40E-05 Genome-wide association analysis of serum iron in the InCHIANTI and the Baltimore Longitudinal Study of Aging (BLSA) dbGaP|2876
NM_201551 NELL1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12295951 2.04E-05 NBL-GWAS version 2 dbGaP|2895
NM_201559 FOXO3 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs9480865 7.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_201559 FOXO3 21216879 http://www.ncbi.nlm.nih.gov/pubmed/21216879 Insulin-Like Growth Factor I rs2153960 5.00E-07 A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. NHGRI|-1
NM_201570 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 1.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201570 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 7.00E-07 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201570 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs11014166 6.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201570 CACNB2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Blood Pressure rs7069923 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_201570 CACNB2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 C-Reactive Protein rs7076247 6.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_201570 CACNB2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17661538 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_201570 CACNB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4748442 9.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_201571 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 1.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201571 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 7.00E-07 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201571 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs11014166 6.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201571 CACNB2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Blood Pressure rs7069923 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_201571 CACNB2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 C-Reactive Protein rs7076247 6.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_201571 CACNB2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17661538 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_201571 CACNB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4748442 9.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_201572 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 1.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201572 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 7.00E-07 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201572 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs11014166 6.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201572 CACNB2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Blood Pressure rs7069923 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_201572 CACNB2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 C-Reactive Protein rs7076247 6.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_201572 CACNB2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17661538 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_201572 CACNB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4748442 9.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_201575 SEZ6L2 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Waist Circumference rs4787483 2.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_201590 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 1.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201590 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 7.00E-07 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201590 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs11014166 6.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201590 CACNB2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Blood Pressure rs7069923 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_201590 CACNB2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 C-Reactive Protein rs7076247 6.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_201590 CACNB2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17661538 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_201590 CACNB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4748442 9.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_201591 GPM6A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1495714 1.93E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_201591 GPM6A 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs7687921 4.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_201591 GPM6A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4690647 1.13E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_201592 GPM6A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs1495714 1.93E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_201592 GPM6A 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality rs7687921 4.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_201592 GPM6A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs4690647 1.13E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_201593 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 1.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201593 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 7.00E-07 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201593 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs11014166 6.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201593 CACNB2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Blood Pressure rs7069923 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_201593 CACNB2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 C-Reactive Protein rs7076247 6.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_201593 CACNB2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17661538 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_201593 CACNB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4748442 9.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_201596 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 1.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201596 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 7.00E-07 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201596 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs11014166 6.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201596 CACNB2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Blood Pressure rs7069923 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_201596 CACNB2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 C-Reactive Protein rs7076247 6.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_201596 CACNB2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17661538 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_201596 CACNB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4748442 9.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_201597 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 1.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201597 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Blood Pressure rs11014166 7.00E-07 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201597 CACNB2 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Hypertension rs11014166 6.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_201597 CACNB2 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Blood Pressure rs7069923 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_201597 CACNB2 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 C-Reactive Protein rs7076247 6.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_201597 CACNB2 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs17661538 1.00E-06 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NM_201597 CACNB2 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4748442 9.19E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_201630 LRRN2 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs12143943 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_201631 TGM5 19654303 http://www.ncbi.nlm.nih.gov/pubmed/19654303 Lung Neoplasms rs748404 1.00E-06 Deciphering the impact of common genetic variation on lung cancer risk: a genome-wide association study. NHGRI|-1
NM_201653 CHIA 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs17654531 1.16E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_203283 RBPJ 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs10517086 5.00E-10 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_203283 RBPJ 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs874040 1.00E-16 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_203284 RBPJ 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs10517086 5.00E-10 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_203284 RBPJ 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs874040 1.00E-16 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_203289 POU5F1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9501063 2.29E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_203289 POU5F1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs9263800 6.55E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_203289 POU5F1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3130931 1.14E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_203289 POU5F1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs9263804 1.34E-08 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_203289 POU5F1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs113112186 2.97E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_203289 POU5F1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3130501 3.87E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_203289 POU5F1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3132524 8.72E-09 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_203291 RBBP8 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs4331426 7.00E-09 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_203291 RBBP8 20364137 http://www.ncbi.nlm.nih.gov/pubmed/20364137 Intracranial Aneurysm rs11661542 1.00E-12 Genome-wide association study of intracranial aneurysm identifies three new risk loci. NHGRI|-1
NM_203292 RBBP8 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs4331426 7.00E-09 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_203292 RBBP8 20364137 http://www.ncbi.nlm.nih.gov/pubmed/20364137 Intracranial Aneurysm rs11661542 1.00E-12 Genome-wide association study of intracranial aneurysm identifies three new risk loci. NHGRI|-1
NM_203293 TRIM7 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs1279750 2.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_203294 TRIM7 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs1279750 2.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_203295 TRIM7 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs1279750 2.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_203296 TRIM7 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs1279750 2.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_203297 TRIM7 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs1279750 2.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_203301 FBXO33 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2415603 3.27E-06 NBL-GWAS version 2 dbGaP|2895
NM_203327 SLC23A2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6107541 1.72E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_203327 SLC23A2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6116558 5.62E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_203327 SLC23A2 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs6107546 8.27E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_203339 CLU 19734902 http://www.ncbi.nlm.nih.gov/pubmed/19734902 Alzheimer Disease rs11136000 9.00E-10 Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease. NHGRI|-1
NM_203339 CLU 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Heart Failure rs11136000 3.50E-04 Genome-wide association between genotype and incident heart failure in African-American participants dbGaP|2885
NM_203339 CLU 21460841 http://www.ncbi.nlm.nih.gov/pubmed/21460841 Alzheimer Disease rs1532278 8.00E-08 "Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease." NHGRI|-1
NM_203339 CLU 21627779 http://www.ncbi.nlm.nih.gov/pubmed/21627779 Alzheimer Disease rs569214 4.00E-08 "The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease." NHGRI|-1
NM_203339 CLU 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs17466684 7.00E-07 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_203349 SHC4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs8023445 1.12E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NM_203349 SHC4 21621269 http://www.ncbi.nlm.nih.gov/pubmed/21621269 "Depressive Disorder, Major" rs8023445 2.00E-06 Genome-wide association analysis of gender differences in major depressive disorder in the Netherlands NESDA and NTR population-based samples. NHGRI|-1
NM_203351 MAP3K3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs7209435 7.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_203371 FIBIN 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs4431984 4.62E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NM_203394 E2F7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1520799 3.08E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_203394 E2F7 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs1402279 5.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_203395 IYD 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic Disorder rs9372078 5.00E-07 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_203395 IYD 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Carbohydrates rs1591830 1.00E-07 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NM_203403 C9orf150 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs12379024 3.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_203403 C9orf150 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs13288636 5.70E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_203403 C9orf150 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs13288681 7.20E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_203416 CD163 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Creatine Kinase rs7136716 3.00E-26 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_203425 C17orf82 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs2079795 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_203425 C17orf82 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs757608 6.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_203444 ABCB9 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs7296418 2.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_203459 CAMSAP1L1 19389651 http://www.ncbi.nlm.nih.gov/pubmed/19389651 Electrocardiography rs7512898 5.00E-06 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. NHGRI|-1
NM_203463 LASS6 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 "Arthritis, Rheumatoid" rs13393173 4.00E-06 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_203463 LASS6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs10930335 9.60E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_203463 LASS6 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs2102808 4.00E-10 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_203463 LASS6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs16855271 9.00E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NM_203487 PCDH9 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17081231 7.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_203487 PCDH9 17903300 http://www.ncbi.nlm.nih.gov/pubmed/17903300 Body Mass Index rs1333026 8.00E-06 Genome-wide association to body mass index and waist circumference: the Framingham Heart Study 100K project. NHGRI|-1
NM_203487 PCDH9 20686608 http://www.ncbi.nlm.nih.gov/pubmed/20686608 Pancreatic Neoplasms rs1585440 9.00E-06 Genome-wide association study of pancreatic cancer in Japanese population. NHGRI|-1
NM_203506 GRB2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs16967789 1.10E-06 NBL-GWAS version 1 dbGaP|2845
NM_203506 GRB2 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs9892996 2.23E-07 NBL-GWAS version 1 dbGaP|2845
NM_205768 ZNF238 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs10927101 2.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_205768 ZNF238 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs476141 1.00E-07 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_205768 ZNF238 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1000543 1.25E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_205768 ZNF238 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2454222 6.14E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_205768 ZNF238 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2454221 8.28E-06 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_205768 ZNF238 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs2047137 9.15E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NM_205837 LST1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9267502 3.79E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_205838 LST1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9267502 3.79E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_205839 LST1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9267502 3.79E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_205840 LST1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9267502 3.79E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NM_205843 NFIC 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs7507204 4.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_205843 NFIC 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs11669592 4.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_205848 SYT6 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs2774292 3.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_205848 SYT6 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs6657718 3.38E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_205849 FAM9B 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs1024443 6.38E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_205850 SLC24A5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1426654 1.42E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_205850 SLC24A5 17999355 http://www.ncbi.nlm.nih.gov/pubmed/17999355 Skin Pigmentation rs1834640 1.00E-50 A genomewide association study of skin pigmentation in a South Asian population. NHGRI|-1
NM_205854 SFTA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2844652 7.62E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_205854 SFTA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2532934 2.37E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_205854 SFTA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs2532934 8.78E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NM_205854 SFTA2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2532929 1.51E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2737621 3.42E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs60636333 1.48E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs60636333 2.64E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs3790844 2.45E-10 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_205860 NR5A2 20101243 http://www.ncbi.nlm.nih.gov/pubmed/20101243 Pancreatic Neoplasms rs3790844 2.00E-10 "A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33." NHGRI|-1
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs3790843 6.69E-09 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2821367 1.89E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs3828112 3.78E-05 NBL-GWAS version 2 dbGaP|2895
NM_205860 NR5A2 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs16844716 9.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs17664308 1.48E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_205860 NR5A2 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs2363451 6.17E-07 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs12029406 1.04E-07 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4465241 4.79E-07 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10919791 6.37E-10 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs4244145 1.98E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2816939 9.58E-06 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_205860 NR5A2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs2821347 1.16E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NM_205862 UGT1A6 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1604144 4.75E-05 NBL-GWAS version 2 dbGaP|2895
NM_205862 UGT1A6 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin rs887829 1.00E-69 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_205862 UGT1A6 19414484 http://www.ncbi.nlm.nih.gov/pubmed/19414484 Bilirubin rs6742078 5E-324 Genome-wide association meta-analysis for total serum bilirubin levels. NHGRI|-1
NM_205862 UGT1A6 21646302 http://www.ncbi.nlm.nih.gov/pubmed/21646302 Bilirubin rs4148325 5.00E-62 Mayo genome consortia: a genotype-phenotype resource for genome-wide association studies with an application to the analysis of circulating bilirubin levels. NHGRI|-1
NM_205863 PARD3B 20694014 http://www.ncbi.nlm.nih.gov/pubmed/20694014 Tuberculosis rs2335704 2.00E-06 Genome-wide association analyses identifies a susceptibility locus for tuberculosis on chromosome 18q11.2. NHGRI|-1
NM_205863 PARD3B 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs2276677 8.56E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_205863 PARD3B 18471798 http://www.ncbi.nlm.nih.gov/pubmed/18471798 "Osteoarthritis, Knee" rs1207421 6.00E-06 Genome-wide association scan identifies a prostaglandin-endoperoxide synthase 2 variant involved in risk of knee osteoarthritis. NHGRI|-1
NM_205863 PARD3B 21502085 http://www.ncbi.nlm.nih.gov/pubmed/21502085 Acquired Immunodeficiency Syndrome rs11884476 3.00E-09 Genome-wide association study implicates PARD3B-based AIDS restriction. NHGRI|-1
NM_205863 PARD3B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7421114 9.89E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_206594 ESRRG 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs12757165 1.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_206594 ESRRG 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs1436900 7.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_206594 ESRRG 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs1497828 4.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_206595 ESRRG 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs12757165 1.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_206595 ESRRG 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs1436900 7.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NM_206595 ESRRG 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs1497828 4.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_206808 CLYBL 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs7992643 5.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_206809 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3135050 2.42E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206809 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071653 2.34E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206809 MOG 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal Neoplasms rs29232 9.00E-17 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_206809 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3131854 2.54E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206810 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3135050 2.42E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206810 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071653 2.34E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206810 MOG 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal Neoplasms rs29232 9.00E-17 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_206810 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3131854 2.54E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206811 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3135050 2.42E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206811 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071653 2.34E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206811 MOG 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal Neoplasms rs29232 9.00E-17 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_206811 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3131854 2.54E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206812 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3135050 2.42E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206812 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071653 2.34E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206812 MOG 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal Neoplasms rs29232 9.00E-17 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_206812 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3131854 2.54E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206813 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3135050 2.42E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206813 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071653 2.34E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206813 MOG 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal Neoplasms rs29232 9.00E-17 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_206813 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3131854 2.54E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206814 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3135050 2.42E-11 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206814 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2071653 2.34E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206814 MOG 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal Neoplasms rs29232 9.00E-17 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_206814 MOG 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3131854 2.54E-08 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NM_206824 VKORC1 19300499 http://www.ncbi.nlm.nih.gov/pubmed/19300499 Warfarin rs9923231 3.00E-181 "A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose." NHGRI|-1
NM_206824 VKORC1 20833655 http://www.ncbi.nlm.nih.gov/pubmed/20833655 Warfarin rs9923231 9.00E-31 Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese. NHGRI|-1
NM_206827 RASL11A 17903306 http://www.ncbi.nlm.nih.gov/pubmed/17903306 Electrocardiography rs10507380 8.00E-06 Genome-wide association study of electrocardiographic and heart rate variability traits: the Framingham Heart Study. NHGRI|-1
NM_206827 RASL11A 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs9512637 1.00E-07 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_206836 PECI 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs6942328 1.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NM_206837 OSCP1 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs6702784 4.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_206840 NVL 21042317 http://www.ncbi.nlm.nih.gov/pubmed/21042317 "Depressive Disorder, Major" rs11579964 4.00E-06 "Genome-wide association study of major depressive disorder: new results, meta-analysis, and lessons learned." NHGRI|-1
NM_206852 RTN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17804446 1.83E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_206852 RTN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11158264 2.54E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_206853 QKI 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 "Arthritis, Rheumatoid" rs10945919 3.00E-07 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_206853 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9356147 3.45E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206853 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs10428875 8.47E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206853 QKI 20516156 http://www.ncbi.nlm.nih.gov/pubmed/20516156 "Depressive Disorder, Major" rs4709845 9.00E-06 Genome-wide association study of major recurrent depression in the U.K. population. NHGRI|-1
NM_206853 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2201806 1.23E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206853 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6455970 2.15E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206853 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9459317 6.76E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206853 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1764053 5.00E-16 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206853 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1923608 7.61E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206853 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs16897566 2.75E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206854 QKI 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 "Arthritis, Rheumatoid" rs10945919 3.00E-07 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_206854 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9356147 3.45E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206854 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs10428875 8.47E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206854 QKI 20516156 http://www.ncbi.nlm.nih.gov/pubmed/20516156 "Depressive Disorder, Major" rs4709845 9.00E-06 Genome-wide association study of major recurrent depression in the U.K. population. NHGRI|-1
NM_206854 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2201806 1.23E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206854 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6455970 2.15E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206854 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9459317 6.76E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206854 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1764053 5.00E-16 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206854 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1923608 7.61E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206854 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs16897566 2.75E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206855 QKI 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 "Arthritis, Rheumatoid" rs10945919 3.00E-07 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_206855 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9356147 3.45E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206855 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs10428875 8.47E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206855 QKI 20516156 http://www.ncbi.nlm.nih.gov/pubmed/20516156 "Depressive Disorder, Major" rs4709845 9.00E-06 Genome-wide association study of major recurrent depression in the U.K. population. NHGRI|-1
NM_206855 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2201806 1.23E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206855 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6455970 2.15E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206855 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9459317 6.76E-14 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206855 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1764053 5.00E-16 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206855 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs1923608 7.61E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206855 QKI 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs16897566 2.75E-09 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NM_206857 RTN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs17804446 1.83E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_206857 RTN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs11158264 2.54E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_206909 PSD3 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4921617 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_206909 PSD3 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs4646249 7.28E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NM_206909 PSD3 21572414 http://www.ncbi.nlm.nih.gov/pubmed/21572414 Metabolism rs4921914 1.00E-28 A genome-wide association study of metabolic traits in human urine. NHGRI|-1
NM_206909 PSD3 20972438 http://www.ncbi.nlm.nih.gov/pubmed/20972438 Urinary Bladder Neoplasms rs1495741 4.00E-11 A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci. NHGRI|-1
NM_206918 DEGS2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs7157599 1.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_206921 C6orf204 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs12210810 2.00E-17 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_206921 C6orf204 19587794 http://www.ncbi.nlm.nih.gov/pubmed/19587794 "Arrhythmias, Cardiac" rs11153730 2.00E-29 Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies. NHGRI|-1
NM_206921 C6orf204 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs11153730 1.00E-18 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_206921 C6orf204 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs11970286 2.00E-24 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_206921 C6orf204 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs11970286 8.00E-07 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_206925 CA12 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart Failure rs10519210 1.00E-08 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_206937 LIG4 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention Deficit and Disruptive Behavior Disorders rs10492664 1.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_206943 LTBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs4670322 5.13E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NM_206943 LTBP1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs3769528 8.00E-08 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_206943 LTBP1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Body Height rs41464348 7.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_206944 TRPM3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4745062 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_206944 TRPM3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12350232 8.34E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_206945 TRPM3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4745062 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_206945 TRPM3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12350232 8.34E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_206946 TRPM3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4745062 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_206946 TRPM3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12350232 8.34E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_206947 TRPM3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4745062 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_206947 TRPM3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12350232 8.34E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_206948 TRPM3 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs4745062 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NM_206948 TRPM3 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs12350232 8.34E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_206949 IFI27L1 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Body Weight rs7157940 3.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_206996 SPAG17 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Body Height rs17038182 5.00E-07 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_206996 SPAG17 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs12735613 4.00E-11 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_206997 GPR152 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs949252 5.01E-07 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_206997 GPR152 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs1638558 1.44E-05 "Genome-Wide Allelic Association of AMD Status in Illumina 100k Chip (Pre-computed)" dbGaP|1
NM_206999 CNOT1 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs37062 1.00E-06 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_206999 CNOT1 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs37062 3.00E-25 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_206999 CNOT1 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs7188697 7.00E-25 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_207002 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_207002 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_207003 BCL2L11 21533175 http://www.ncbi.nlm.nih.gov/pubmed/21533175 Dehydroepiandrosterone Sulfate rs6738028 2.00E-08 Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms. NHGRI|-1
NM_207003 BCL2L11 21151127 http://www.ncbi.nlm.nih.gov/pubmed/21151127 "Cholangitis, Sclerosing" rs6720394 4.00E-08 Genome-wide association analysis in primary sclerosing cholangitis identifies two non-HLA susceptibility loci. NHGRI|-1
NM_207015 NAALADL2 19132087 http://www.ncbi.nlm.nih.gov/pubmed/19132087 Mucocutaneous Lymph Node Syndrome rs17531088 1.00E-06 A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease. NHGRI|-1
NM_207015 NAALADL2 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs1463525 8.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_207036 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7176873 1.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207036 TCF12 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2733332 4.41E-06 NBL-GWAS version 1 dbGaP|2845
NM_207036 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs16977243 2.74E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207036 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2733333 9.31E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207036 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7175191 1.64E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207037 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7176873 1.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207037 TCF12 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2733332 4.41E-06 NBL-GWAS version 1 dbGaP|2845
NM_207037 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs16977243 2.74E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207037 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2733333 9.31E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207037 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7175191 1.64E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207038 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7176873 1.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207038 TCF12 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2733332 4.41E-06 NBL-GWAS version 1 dbGaP|2845
NM_207038 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs16977243 2.74E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207038 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2733333 9.31E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207038 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7175191 1.64E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207040 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7176873 1.15E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207040 TCF12 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs2733332 4.41E-06 NBL-GWAS version 1 dbGaP|2845
NM_207040 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs16977243 2.74E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207040 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs2733333 9.31E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207040 TCF12 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs7175191 1.64E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NM_207111 RNF216 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2017620 2.76E-05 NBL-GWAS version 2 dbGaP|2895
NM_207113 SLC37A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7777468 6.51E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_207113 SLC37A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6955063 4.02E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_207113 SLC37A3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6947516 6.25E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NM_207116 RNF216 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs2017620 2.76E-05 NBL-GWAS version 2 dbGaP|2895
NM_207170 SYF2 21743469 http://www.ncbi.nlm.nih.gov/pubmed/21743469 "Spondylitis, Ankylosing" rs11249215 9.00E-11 Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. NHGRI|-1
NM_207170 SYF2 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs10903122 2.00E-10 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_207174 ABCG1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Personality rs425215 8.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_207299 LPPR1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs2417226 8.20E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_207303 ATRNL1 21130836 http://www.ncbi.nlm.nih.gov/pubmed/21130836 Neurobehavioral Manifestations rs10490919 2.00E-06 Whole genome association scan for genetic polymorphisms influencing information processing speed. NHGRI|-1
NM_207304 MBNL2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs9516905 5.94E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_207304 MBNL2 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs9556711 2.00E-06 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_207304 MBNL2 21529783 http://www.ncbi.nlm.nih.gov/pubmed/21529783 Alcoholism rs9556711 8.00E-07 A Quantitative-Trait Genome-Wide Association Study of Alcoholism Risk in the Community: Findings and Implications. NHGRI|-1
NM_207311 CCDC64 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs11064994 6.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_207322 C2CD4A 20818381 http://www.ncbi.nlm.nih.gov/pubmed/20818381 "Diabetes Mellitus, Type 2" rs7172432 9.00E-14 A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B. NHGRI|-1
NM_207322 C2CD4A 20862305 http://www.ncbi.nlm.nih.gov/pubmed/20862305 "Diabetes Mellitus, Type 2" rs1436955 7.00E-07 Identification of new genetic risk variants for type 2 diabetes. NHGRI|-1
NM_207322 C2CD4A 18057069 http://www.ncbi.nlm.nih.gov/pubmed/18057069 Amyotrophic Lateral Sclerosis rs6494311 2.18E-04 Genomewide Association in Population-Based Samples dbGaP|2851
NM_207322 C2CD4A 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs11071657 4.00E-08 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NM_207325 DPY19L3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2012353 2.42E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_207325 DPY19L3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs16967057 2.87E-06 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_207325 DPY19L3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2111504 1.57E-07 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NM_207325 DPY19L3 19488044 http://www.ncbi.nlm.nih.gov/pubmed/19488044 Bipolar Disorder rs2111504 2.00E-06 Genome-wide association study of bipolar disorder in European American and African American individuals. NHGRI|-1
NM_207332 ERICH1 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4876063 8.39E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_207332 ERICH1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1703940 1.12E-07 NBL-GWAS version 2 dbGaP|2895
NM_207342 MGC87042 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs17364464 4.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NM_207356 C1orf174 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs4400585 1.58E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NM_207356 C1orf174 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Factor VII rs966321 8.00E-06 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_207356 C1orf174 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6679220 1.00E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_207356 C1orf174 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4654432 7.20E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_207356 C1orf174 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs4654433 9.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_207361 FREM2 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Waist-Hip Ratio rs9315632 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_207362 C2orf55 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar Disorder rs6733011 3.00E-06 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_207363 NCKAP5 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1437898 8.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_207363 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6749561 3.67E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207363 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs17800749 1.81E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207363 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10496702 1.20E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207363 NCKAP5 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs10496702 7.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_207363 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13430905 1.07E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207363 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13431418 1.15E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207363 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7600871 1.20E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207363 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10193871 6.98E-06 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207363 NCKAP5 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs7577925 3.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_207363 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13399558 1.34E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207363 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13412008 2.65E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207363 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12469282 2.24E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207363 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6711228 6.58E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_207386 SHISA6 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs4792139 9.71E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NM_207396 RNF207 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs846111 1.00E-16 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_207396 RNF207 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs846111 4.00E-16 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_207410 GFRAL 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs9367630 1.00E-07 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_207412 C8orf86 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs16887478 1.63E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_207414 FLJ43860 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs13263959 8.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_207426 FOXI2 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11018214 2.99E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_207435 C12orf76 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs11064896 8.57E-05 Genome-wide association study of soluble E-selectin dbGaP|2871
NM_207440 C13orf35 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 "Hemoglobin A, Glycosylated" rs7998202 5.00E-09 Common variants at 10 genomic loci influence hemoglobin AG??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_207444 C15orf53 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs12899449 4.00E-07 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_207444 C15orf53 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2643217 6.67E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207444 C15orf53 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs2624265 4.31E-07 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_207444 C15orf53 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Triglycerides rs2624265 4.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_207444 C15orf53 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs12907914 1.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_207444 C15orf53 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs12912251 1.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NM_207445 C15orf54 18711365 http://www.ncbi.nlm.nih.gov/pubmed/18711365 Bipolar Disorder rs12899449 4.00E-07 Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder. NHGRI|-1
NM_207445 C15orf54 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2643217 6.67E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207445 C15orf54 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Triglycerides rs2624265 4.31E-07 Genomewide association analysis of triglycerides (TG) in a birth cohort from a founder population dbGaP|2904
NM_207445 C15orf54 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Triglycerides rs2624265 4.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_207445 C15orf54 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs12907914 1.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_207446 FAM174B 21160409 http://www.ncbi.nlm.nih.gov/pubmed/21160409 HIV-1 rs285757 7.00E-06 Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population. NHGRI|-1
NM_207446 FAM174B 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Vital Capacity rs1455782 4.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NM_207468 FAM177B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9286760 6.68E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NM_207468 FAM177B 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs6683071 4.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NM_207481 NCKAP5 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs1437898 8.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_207481 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6749561 3.67E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207481 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs17800749 1.81E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207481 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10496702 1.20E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207481 NCKAP5 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs10496702 7.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_207481 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13430905 1.07E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207481 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13431418 1.15E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207481 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7600871 1.20E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207481 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10193871 6.98E-06 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207481 NCKAP5 18821565 http://www.ncbi.nlm.nih.gov/pubmed/18821565 Attention Deficit Disorder with Hyperactivity rs7577925 3.00E-06 Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. NHGRI|-1
NM_207481 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13399558 1.34E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207481 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs13412008 2.65E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207481 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs12469282 2.24E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207481 NCKAP5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6711228 6.58E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_207491 FAM190A 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs41519045 1.48E-11 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NM_207491 FAM190A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7697633 9.31E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NM_207491 FAM190A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs12233759 8.45E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_207506 SAMD12 16252231 http://www.ncbi.nlm.nih.gov/pubmed/16252231 Parkinson Disease rs723268 8.86E-05 Tier1 Genome Association of Parkinson's Disease Using Discordant Sib-Pairs dbGaP|2840
NM_207517 ADAMTSL3 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs10906982 2.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_207517 ADAMTSL3 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs10906982 5.00E-07 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_207517 ADAMTSL3 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body Height rs7183263 4.00E-07 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_207517 ADAMTSL3 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs4842838 1.00E-07 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_207517 ADAMTSL3 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Body Height rs4842838 3.00E-08 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_207517 ADAMTSL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs7178655 7.22E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207517 ADAMTSL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs6603020 2.57E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NM_207517 ADAMTSL3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs2554380 9.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_207578 PRKACB 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs1085093 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_207627 ABCG1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Personality rs425215 8.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_207628 ABCG1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Personality rs425215 8.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_207629 ABCG1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Personality rs425215 8.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_207644 C22orf36 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs4820599 4.00E-11 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_207645 C11orf87 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs6589076 1.05E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_207645 C11orf87 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs875430 4.40E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_207645 C11orf87 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs2716040 6.90E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NM_212460 ARL4A 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs732577 4.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NM_212474 FN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1250255 3.21E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_212476 FN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1250255 3.21E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_212478 FN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1250255 3.21E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_212481 ARID5A 21046636 http://www.ncbi.nlm.nih.gov/pubmed/21046636 Brain Waves rs4907240 4.00E-06 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. NHGRI|-1
NM_212482 FN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs1250255 3.21E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NM_212556 ASB18 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, LDL" rs13390159 2.00E-07 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_213569 NEBL 21310492 http://www.ncbi.nlm.nih.gov/pubmed/21310492 Diabetic Retinopathy rs12219125 9.00E-09 Genome-wide association study of diabetic retinopathy in a Taiwanese population. NHGRI|-1
NM_213569 NEBL 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs12772794 7.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NM_213569 NEBL 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs16920624 7.00E-07 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NM_213569 NEBL 20610895 http://www.ncbi.nlm.nih.gov/pubmed/20610895 Vascular Diseases rs2359536 2.00E-06 Identification of evidence suggestive of an association with peripheral arterial disease at the OSBPL10 locus by genome-wide investigation in the Japanese population. NHGRI|-1
NM_213594 RFX4 21084426 http://www.ncbi.nlm.nih.gov/pubmed/21084426 Parkinson Disease rs4964469 2.00E-07 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. NHGRI|-1
NM_213594 RFX4 17903297 http://www.ncbi.nlm.nih.gov/pubmed/17903297 Neuropsychological Tests rs3891355 3.00E-06 Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study. NHGRI|-1
NM_213599 ANO5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12295951 2.04E-05 NBL-GWAS version 2 dbGaP|2895
NM_213631 C20orf132 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs8115854 2.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_213631 C20orf132 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs6031882 6.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_213632 C20orf132 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs8115854 2.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_213632 C20orf132 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampus rs6031882 6.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_213662 STAT3 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn Disease rs744166 7.00E-12 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_213662 STAT3 20159113 http://www.ncbi.nlm.nih.gov/pubmed/20159113 Multiple Sclerosis rs744166 3.00E-10 Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. NHGRI|-1
NM_213725 RPLP1 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs17374222 2.00E-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_213725 RPLP1 17903304 http://www.ncbi.nlm.nih.gov/pubmed/17903304 Atrial Fibrillation rs4776472 8.00E-06 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. NHGRI|-1
NM_213725 RPLP1 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs7176508 5.00E-12 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NR_000006 RPL5 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs6604026 3.00E-06 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NR_000006 RPL5 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs6604026 8.00E-06 Risk alleles for multiple sclerosis identified by a genomewide study. NHGRI|-1
NR_000006 RPL5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs6604026 1.01E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_000006 RPL5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10782945 7.36E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_000026 RPL3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs2413583 1.00E-26 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NR_000026 RPL3 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs968451 1.00E-09 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NR_000026 RPL3 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs54211 8.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NR_000028 RPL3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs2413583 1.00E-26 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NR_000028 RPL3 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs968451 1.00E-09 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NR_000028 RPL3 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs54211 8.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NR_002212 NUDT4 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs1836127 3.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NR_002439 RPL3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs2413583 1.00E-26 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NR_002439 RPL3 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs968451 1.00E-09 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NR_002439 RPL3 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs54211 8.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NR_002742 C6orf48 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4711279 1.06E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_002742 C6orf48 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 rs9368699 5.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NR_002742 C6orf48 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs17207629 3.36E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_002742 C6orf48 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs733539 4.64E-06 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NR_002742 C6orf48 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs733539 5.49E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_003065 BAT1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3115537 2.46E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NR_003065 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3093978 8.82E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_003065 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3093948 8.72E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_003065 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3093976 1.03E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_003065 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3130057 1.07E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_003065 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2734583 5.29E-68 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NR_003065 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3130058 6.23E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_003065 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2516393 8.82E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_003065 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2239709 4.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_003065 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2251824 5.97E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_003090 MOBP 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs1768208 5.00E-17 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NR_003090 MOBP 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs816488 4.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NR_003090 MOBP 18839057 http://www.ncbi.nlm.nih.gov/pubmed/18839057 Attention Deficit Disorder with Hyperactivity rs864643 1.00E-08 Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies. NHGRI|-1
NR_003092 E2F6 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs6716724 6.00E-07 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NR_003129 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3134945 1.24E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_003129 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3134945 4.06E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NR_003129 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs3132965 8.39E-16 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NR_003129 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130349 5.68E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_003129 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130349 9.28E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NR_003129 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3134943 2.82E-105 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NR_003129 RNF5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs8365 1.09E-17 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NR_003144 ANP32A 21642993 http://www.ncbi.nlm.nih.gov/pubmed/21642993 Esophageal Neoplasms rs8030672 1.00E-11 Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations. NHGRI|-1
NR_003189 SYS1 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs1008953 1.00E-07 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NR_003259 GNAS 21046636 http://www.ncbi.nlm.nih.gov/pubmed/21046636 Brain Waves rs13831 6.00E-06 Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. NHGRI|-1
NR_003512 IGF2 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 "Diabetes Mellitus, Type 1" rs3741208 2.00E-07 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NR_003512 IGF2 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 "Diabetes Mellitus, Type 1" rs1004446 4.00E-09 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NR_003955 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2036902 9.88E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_003955 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs13157992 9.03E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_003955 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7720960 7.28E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_003955 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7378969 6.04E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_003955 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1016620 9.80E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_003955 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs559096 9.08E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_003955 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs1674512 9.15E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_003955 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4865676 9.06E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_003955 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10064702 9.15E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_003955 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7710841 9.06E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_003955 EMB 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs10042504 9.15E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_023315 ASZ1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary Artery Disease rs7808424 1.00E-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NR_023316 ACSF3 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs3743979 2.02E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NR_023349 TSEN15 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs2274432 8.00E-09 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NR_023359 CABLES1 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs11082304 6.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NR_023359 CABLES1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs4800148 4.00E-09 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NR_023359 CABLES1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Body Height rs4369779 3.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NR_023359 CABLES1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs4369779 6.86E-04 Genome-wide association between genotype and incident stroke in participants of primarily self-described European ancestry dbGaP|2886
NR_024040 CSGALNACT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6983139 2.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NR_024040 CSGALNACT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs6983139 5.10E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NR_024094 RANBP6 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs1342326 9.00E-10 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NR_024095 RANBP6 20860503 http://www.ncbi.nlm.nih.gov/pubmed/20860503 Asthma rs1342326 9.00E-10 "A large-scale, consortium-based genomewide association study of asthma." NHGRI|-1
NR_024099 ESRRG 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs12757165 1.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NR_024099 ESRRG 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs1436900 7.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NR_024099 ESRRG 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 "Diabetes Mellitus, Type 2" rs1497828 4.00E-06 Genome-wide association scan for survival on dialysis in african-americans with type 2 diabetes. NHGRI|-1
NR_024122 PBX3 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs888219 2.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NR_024123 PBX3 19721433 http://www.ncbi.nlm.nih.gov/pubmed/19721433 Risperidone rs888219 2.00E-07 Genome-wide pharmacogenomic analysis of response to treatment with antipsychotics. NHGRI|-1
NR_024152 MFAP3 21701570 http://www.ncbi.nlm.nih.gov/pubmed/21701570 Body Mass Index rs2033195 6.00E-06 Genome-Wide Association of BMI in African Americans. NHGRI|-1
NR_024164 ZNF323 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs853679 2.52E-10 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NR_024164 ZNF323 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs853676 5.22E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NR_024164 ZNF323 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs853676 6.14E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NR_024168 TLR4 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Stomach Neoplasms rs876347 2.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NR_024168 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1335258 1.77E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024168 TLR4 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs1572299 4.00E-06 Common variants conferring risk of schizophrenia. NHGRI|-1
NR_024168 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10984107 4.62E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NR_024168 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11789399 4.30E-06 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NR_024168 TLR4 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11789399 6.00E-09 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NR_024168 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11789399 1.60E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024168 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11789407 1.69E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NR_024168 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11789407 2.17E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024168 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10759986 2.89E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024168 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10733631 2.07E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024168 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10759987 3.57E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024168 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7866602 5.24E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024168 TLR4 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12237612 9.36E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NR_024169 TLR4 19875103 http://www.ncbi.nlm.nih.gov/pubmed/19875103 Stomach Neoplasms rs876347 2.00E-06 Genomewide association study of movement-related adverse antipsychotic effects. NHGRI|-1
NR_024169 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs1335258 1.77E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024169 TLR4 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs1572299 4.00E-06 Common variants conferring risk of schizophrenia. NHGRI|-1
NR_024169 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs10984107 4.62E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NR_024169 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11789399 4.30E-06 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NR_024169 TLR4 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs11789399 6.00E-09 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NR_024169 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11789399 1.60E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024169 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs11789407 1.69E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NR_024169 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs11789407 2.17E-06 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024169 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10759986 2.89E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024169 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10733631 2.07E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024169 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs10759987 3.57E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024169 TLR4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs7866602 5.24E-05 "Genome Wide Association Study of Schizophrenia in European American Population (US) (Pre-computed)" dbGaP|2857
NR_024169 TLR4 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs12237612 9.36E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NR_024171 MDM4 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs12143943 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NR_024179 PDLIM5 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs12500426 1.00E-11 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NR_024179 PDLIM5 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostatic Neoplasms rs17021918 4.00E-15 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NR_024266 CCNT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7297499 5.97E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_024275 MGAT5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs3748900 5.77E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NR_024275 MGAT5 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs2118844 2.78E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NR_024275 MGAT5 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2118844 4.35E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NR_024275 MGAT5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Breast Neoplasms rs6711228 6.58E-05 A genome-wide association study identifies alleles associated with risk of sporadic postmenopausal breast cancer dbGaP|2853
NR_024320 LITAF 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs7203193 3.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NR_024320 LITAF 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 Electrocardiography rs8049607 5.00E-15 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NR_024320 LITAF 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 Electrocardiography rs8049607 6.00E-15 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NR_024386 PLEKHM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11012 2.85E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NR_024386 PLEKHM1 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs11012 6.00E-08 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NR_024386 PLEKHM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11012 8.77E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NR_024460 CCDC66 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip rs2054989 6.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NR_024514 ADAMTS13 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs4962153 8.00E-21 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NR_024514 ADAMTS13 19729612 http://www.ncbi.nlm.nih.gov/pubmed/19729612 E-Selectin rs4962153 8.05E-14 Genome-wide association study of soluble E-selectin dbGaP|2871
NR_024539 POPDC3 21654844 http://www.ncbi.nlm.nih.gov/pubmed/21654844 Multiple Sclerosis rs11962089 8.00E-06 Genome-wide association study of severity in multiple sclerosis. NHGRI|-1
NR_024546 TXNL1 17903305 http://www.ncbi.nlm.nih.gov/pubmed/17903305 Breast Neoplasms rs1978503 1.00E-06 A genome-wide association study of breast and prostate cancer in the NHLBI's Framingham Heart Study. NHGRI|-1
NR_024546 TXNL1 21160409 http://www.ncbi.nlm.nih.gov/pubmed/21160409 HIV-1 rs12604483 7.00E-06 Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population. NHGRI|-1
NR_024546 TXNL1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs2538026 8.91E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NR_024546 TXNL1 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs1229598 7.83E-07 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NR_024548 CRCP 21223598 http://www.ncbi.nlm.nih.gov/pubmed/21223598 Aorta rs875971 4.00E-06 Genome-wide joint SNP and CNV analysis of aortic root diameter in African Americans: the HyperGEN study. NHGRI|-1
NR_024549 DMTF1 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs11773103 1.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NR_024550 DMTF1 20351715 http://www.ncbi.nlm.nih.gov/pubmed/20351715 Bipolar Disorder rs11773103 1.00E-06 Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder. NHGRI|-1
NR_024554 RHOBTB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4132554 7.66E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NR_024555 RHOBTB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4132554 7.66E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NR_024556 RHOBTB1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs4132554 7.66E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NR_024596 C11orf73 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs6592284 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NR_024598 C11orf73 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs6592284 2.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NR_024625 API5 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Electrocardiography rs1484948 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NR_024625 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs12273344 6.51E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NR_024625 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9300039 5.99E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NR_024625 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs9300039 6.00E-08 A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants. NHGRI|-1
NR_024625 API5 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs10501281 5.29E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NR_024625 API5 17362836 http://www.ncbi.nlm.nih.gov/pubmed/17362836 Amyotrophic Lateral Sclerosis rs7928165 3.27E-05 Genome-Wide Genotypic Association of Amyotrophic Lateral Sclerosis dbGaP|2846
NR_024625 API5 19734545 http://www.ncbi.nlm.nih.gov/pubmed/19734545 Psychomotor Performance rs10501293 5.00E-06 A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB. NHGRI|-1
NR_026560 ZNF438 20195266 http://www.ncbi.nlm.nih.gov/pubmed/20195266 Clozapine rs2994684 3.00E-07 Genomewide pharmacogenomic study of metabolic side effects to antipsychotic drugs. NHGRI|-1
NR_026560 ZNF438 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs11008171 7.96E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_026570 MAPRE2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs595086 7.11E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NR_026571 NOX4 20801717 http://www.ncbi.nlm.nih.gov/pubmed/20801717 Amyotrophic Lateral Sclerosis rs1488902 3.00E-06 Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association study. NHGRI|-1
NR_026572 PDE2A 20395239 http://www.ncbi.nlm.nih.gov/pubmed/20395239 Eye rs12418204 5.00E-06 Genome-wide association identifies ATOH7 as a major gene determining human optic disc size. NHGRI|-1
NR_026572 PDE2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs341076 4.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NR_026572 PDE2A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs193170 3.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NR_026586 EFCAB2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4658673 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NR_026587 EFCAB2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4658673 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NR_026590 CDYL 21685187 http://www.ncbi.nlm.nih.gov/pubmed/21685187 "Pulmonary Disease, Chronic Obstructive" rs73717741 3.00E-07 Genome-wide association study of smoking behaviours in patients with COPD. NHGRI|-1
NR_026665 CD58 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple Sclerosis rs1335532 1.00E-07 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NR_026665 CD58 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple Sclerosis rs2300747 3.00E-10 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NR_026665 CD58 21244703 http://www.ncbi.nlm.nih.gov/pubmed/21244703 Multiple Sclerosis rs12025416 1.00E-07 Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data. NHGRI|-1
NR_026671 CD69 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs4763879 2.00E-11 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NR_026672 CD69 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs4763879 2.00E-11 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NR_026678 TMEM79 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs6684514 3.00E-09 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NR_026695 FGF1 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs152528 8.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NR_026696 FGF1 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiomegaly rs152528 8.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NR_026717 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs416002 9.33E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_026717 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs389884 8.47E-87 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NR_026717 STK19 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs389884 2.08E-18 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NR_026717 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs389884 9.42E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NR_026717 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs387608 1.91E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_026717 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs387608 6.95E-09 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NR_026717 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs389883 1.56E-05 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NR_026717 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs389512 2.34E-08 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_026717 STK19 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs389512 9.00E-09 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NR_026718 FOXO3 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple Sclerosis rs9480865 7.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NR_026718 FOXO3 21216879 http://www.ncbi.nlm.nih.gov/pubmed/21216879 Insulin-Like Growth Factor I rs2153960 5.00E-07 A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. NHGRI|-1
NR_026735 GPN1 21386085 http://www.ncbi.nlm.nih.gov/pubmed/21386085 Metabolic Syndrome X rs3749147 1.00E-09 A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. NHGRI|-1
NR_026745 COG6 18369459 http://www.ncbi.nlm.nih.gov/pubmed/18369459 Psoriasis rs7993214 2.00E-06 A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. NHGRI|-1
NR_026745 COG6 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 "Colitis, Ulcerative" rs9548988 3.00E-07 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NR_026745 COG6 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Alanine Transaminase rs10492681 2.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NR_026745 COG6 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs941823 4.00E-12 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NR_026745 COG6 20719862 http://www.ncbi.nlm.nih.gov/pubmed/20719862 Cornea rs2755237 1.00E-08 "New loci associated with central cornea thickness include COL5A1, AKAP13 and AVGR8." NHGRI|-1
NR_026745 COG6 20485516 http://www.ncbi.nlm.nih.gov/pubmed/20485516 Cornea rs2721051 5.00E-10 Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thickness. NHGRI|-1
NR_026799 SH3GL3 18391950 http://www.ncbi.nlm.nih.gov/pubmed/18391950 Body Height rs2562784 6.00E-08 Identification of ten loci associated with height highlights new biological pathways in human growth. NHGRI|-1
NR_026799 SH3GL3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Body Height rs2554380 9.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NR_026858 CHRNA7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4779984 1.58E-05 NBL-GWAS version 2 dbGaP|2895
NR_026858 CHRNA7 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1001555 3.75E-06 NBL-GWAS version 1 dbGaP|2845
NR_026918 PTPN3 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4978813 7.01E-06 NBL-GWAS version 1 dbGaP|2845
NR_027296 IFLTD1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4963910 8.37E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NR_027303 TRIB2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs17551939 8.49E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NR_027303 TRIB2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Mental Disorders rs10929808 4.00E-06 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NR_027303 TRIB2 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 "Diabetes Mellitus, Type 1" rs1534422 2.00E-06 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NR_027307 MEF2B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10896 1.65E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NR_027307 MEF2B 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11669988 6.75E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NR_027322 CAMK1D 20862305 http://www.ncbi.nlm.nih.gov/pubmed/20862305 "Diabetes Mellitus, Type 2" rs10906115 1.00E-08 Identification of new genetic risk variants for type 2 diabetes. NHGRI|-1
NR_027322 CAMK1D 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 "Diabetes Mellitus, Type 2" rs12779790 1.00E-10 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NR_027322 CAMK1D 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11257695 1.67E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NR_027322 CAMK1D 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs11257695 5.30E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NR_027368 POP4 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs6509542 5.41E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NR_027368 POP4 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic Retinopathy rs10403021 2.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NR_027390 GRINL1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs597804 5.59E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_027390 GRINL1A 19609347 http://www.ncbi.nlm.nih.gov/pubmed/19609347 Hypertension rs1550576 3.00E-06 A genome-wide association study of hypertension and blood pressure in African Americans. NHGRI|-1
NR_027409 GOLGA8B 20835239 http://www.ncbi.nlm.nih.gov/pubmed/20835239 Refractive Errors rs634990 2.00E-14 A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14. NHGRI|-1
NR_027410 GOLGA8B 20835239 http://www.ncbi.nlm.nih.gov/pubmed/20835239 Refractive Errors rs634990 2.00E-14 A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14. NHGRI|-1
NR_027449 TBC1D15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs328764 7.52E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NR_027470 CHRNA7 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs4779984 1.58E-05 NBL-GWAS version 2 dbGaP|2895
NR_027470 CHRNA7 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs1001555 3.75E-06 NBL-GWAS version 1 dbGaP|2845
NR_027474 AGXT2L1 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs4956211 1.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NR_027635 SPATA5L1 19430482 http://www.ncbi.nlm.nih.gov/pubmed/19430482 Creatinine rs2467853 6.00E-14 Multiple loci associated with indices of renal function and chronic kidney disease. NHGRI|-1
NR_027672 ADARB1 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Respiratory Function Tests rs2838815 3.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NR_027673 ADARB1 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Respiratory Function Tests rs2838815 3.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NR_027674 ADARB1 17903307 http://www.ncbi.nlm.nih.gov/pubmed/17903307 Respiratory Function Tests rs2838815 3.00E-06 Framingham Heart Study genome-wide association: results for pulmonary function measures. NHGRI|-1
NR_027702 CDK10 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs258322 2.00E-23 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NR_027702 CDK10 19578364 http://www.ncbi.nlm.nih.gov/pubmed/19578364 Melanoma rs258322 3.00E-27 Genome-wide association study identifies three loci associated with melanoma risk. NHGRI|-1
NR_027703 CDK10 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs258322 2.00E-23 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NR_027703 CDK10 19578364 http://www.ncbi.nlm.nih.gov/pubmed/19578364 Melanoma rs258322 3.00E-27 Genome-wide association study identifies three loci associated with melanoma risk. NHGRI|-1
NR_027767 TNIK 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary Disease rs11920719 4.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NR_027767 TNIK 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Schizophrenia rs2088885 6.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NR_027767 TNIK 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Schizophrenia rs13065441 3.16E-05 "Genome Wide Association Study of Schizophrenia in African American Population (US) (Pre-computed)" dbGaP|2859
NR_027774 PLEKHM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11012 2.85E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NR_027774 PLEKHM1 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs11012 6.00E-08 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NR_027774 PLEKHM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11012 8.77E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NR_027780 HMGXB4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2092331 2.28E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_027816 SDK1 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Thyrotropin rs6462411 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NR_027816 SDK1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs882362 6.07E-05 NBL-GWAS version 2 dbGaP|2895
NR_027850 MTX2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2969363 7.66E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NR_027867 PDCD6IP 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs11714343 9.59E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NR_027867 PDCD6IP 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1919624 4.01E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NR_027918 CCDC62 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson Disease rs12817488 3.00E-13 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NR_027932 CLLU1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10219495 5.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NR_027933 CLLU1 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10219495 5.00E-06 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NR_028041 GRM8 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Carotid Artery Diseases rs17691394 9.00E-07 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NR_028041 GRM8 20237162 http://www.ncbi.nlm.nih.gov/pubmed/20237162 Chemokines rs11971186 9.00E-06 "Chemerin, a novel adipokine in the regulation of angiogenesis." NHGRI|-1
NR_028041 GRM8 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression rs17864092 6.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NR_028102 THUMPD2 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs2716734 2.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NR_028102 THUMPD2 18957941 http://www.ncbi.nlm.nih.gov/pubmed/18957941 Personality rs2540226 3.00E-06 Genome-wide association scan for five major dimensions of personality. NHGRI|-1
NR_028292 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NR_028292 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 8.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NR_028292 PTGER3 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs10458561 4.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NR_028293 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NR_028293 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 8.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NR_028293 PTGER3 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs10458561 4.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NR_028294 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 4.65E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NR_028294 PTGER3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs12561944 8.87E-05 GWAS for age of onset of alcohol dependence in European-Americans dbGaP|2893
NR_028294 PTGER3 20921969 http://www.ncbi.nlm.nih.gov/pubmed/20921969 Antipsychotic Agents rs10458561 4.00E-07 Genome-wide association study of antipsychotic-induced QTc interval prolongation. NHGRI|-1
NR_028328 ELMOD1 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Personality rs10431058 8.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NR_028338 TRAF3IP2 20953186 http://www.ncbi.nlm.nih.gov/pubmed/20953186 "Arthritis, Psoriatic" rs33980500 1.00E-20 Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis. NHGRI|-1
NR_028338 TRAF3IP2 20953188 http://www.ncbi.nlm.nih.gov/pubmed/20953188 Psoriasis rs33980500 1.00E-16 Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. NHGRI|-1
NR_028395 DISC1 21483430 http://www.ncbi.nlm.nih.gov/pubmed/21483430 Neuranatomic and neurocognitive phenotypes rs12042938 4.00E-36 Impact of DISC1 variation on neuroanatomical and neurocognitive phenotypes. NHGRI|-1
NR_028395 DISC1 19118814 http://www.ncbi.nlm.nih.gov/pubmed/19118814 Alzheimer Disease rs12044355 9.00E-06 Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease. NHGRI|-1
NR_028395 DISC1 21659360 http://www.ncbi.nlm.nih.gov/pubmed/21659360 "Leukemia, Lymphocytic, Chronic, B-Cell" rs2793086 9.00E-06 Association between SNP-genotype and chronic lymphocytic leukemia outcome in a randomized chemotherapy trial. NHGRI|-1
NR_028395 DISC1 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs16856202 8.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NR_028402 CSRP2BP 21079607 http://www.ncbi.nlm.nih.gov/pubmed/21079607 Anorexia Nervosa rs17725255 2.00E-06 A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa. NHGRI|-1
NR_028406 FXYD5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2285515 7.66E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_028437 UBE2L3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs181359 5.00E-16 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NR_028437 UBE2L3 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs5754217 2.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NR_028437 UBE2L3 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Erythrocyte Indices rs4821112 1.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NR_028437 UBE2L3 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 "Lupus Erythematosus, Systemic" rs131654 1.00E-16 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NR_028588 PECI 21294900 http://www.ncbi.nlm.nih.gov/pubmed/21294900 Uric Acid rs6942328 1.00E-06 A genome-wide association study of serum uric acid in African Americans. NHGRI|-1
NR_029461 LST1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9267502 3.79E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NR_029462 LST1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs9267502 3.79E-19 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NR_029467 SELL 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs12938 6.33E-05 Genome-wide association study of HbA1C in intensive treatment group dbGaP|2881
NR_029467 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs964555 2.34E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_029467 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4987314 1.23E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_029467 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2229569 9.88E-06 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_029467 SELL 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic Lateral Sclerosis rs1131498 4.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NR_029467 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4987285 6.00E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_029467 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2205849 1.40E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_029467 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs4656703 4.48E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_029467 SELL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs3917449 5.35E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_029467 SELL 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Alzheimer Disease rs1569476 3.00E-07 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NR_029496 C9orf3 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs3802458 4.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NR_029696 RTL1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs3825569 3.69E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NR_029699 RTL1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs3825569 3.69E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NR_029965 RTL1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs3825569 3.69E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NR_029966 RTL1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs3825569 3.69E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NR_030173 RTL1 17463248 http://www.ncbi.nlm.nih.gov/pubmed/17463248 "Diabetes Mellitus, Type 2" rs3825569 3.69E-05 Genome-wide Association Analysis of Type 2 Diabetes in Finns dbGaP|2839
NR_030342 C11orf10 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs102275 6.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NR_030342 C11orf10 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn Disease rs102275 2.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NR_030342 C11orf10 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs102275 6.51E-06 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NR_030345 GPRC5A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs1056927 7.24E-05 NBL-GWAS version 2 dbGaP|2895
NR_030345 GPRC5A 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs704225 6.66E-06 NBL-GWAS version 1 dbGaP|2845
NR_030737 TTC3 20463881 http://www.ncbi.nlm.nih.gov/pubmed/20463881 Eye Color rs1003719 2.00E-10 Digital quantification of human eye color highlights genetic association of three new loci. NHGRI|-1
NR_030765 ATP5SL 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Body Height rs17318596 5.00E-16 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NR_030778 WDR65 21460395 http://www.ncbi.nlm.nih.gov/pubmed/21460395 Telomere length rs621559 2.00E-06 A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer. NHGRI|-1
NR_031593 FAM89A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4388693 3.06E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NR_031601 RDBP 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs2072633 1.47E-10 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NR_031601 RDBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4151672 1.74E-09 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_031601 RDBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs4151672 6.10E-10 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NR_031601 RDBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs438999 4.89E-18 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_031601 RDBP 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs438999 5.68E-19 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NR_031692 CPSF6 20673876 http://www.ncbi.nlm.nih.gov/pubmed/20673876 "Depressive Disorder, Major" rs9943849 3.00E-06 "Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression." NHGRI|-1
NR_031719 NFAT5 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs1364063 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NR_031729 FADS1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 "Cholesterol, HDL" rs174546 6.00E-07 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NR_031729 FADS1 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 "Cholesterol, LDL" rs174546 1.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NR_031729 FADS1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lipoproteins, LDL" rs174546 6.38E-06 Genomewide association analysis of low density lipoproteins (LDL) in a birth cohort from a founder population dbGaP|2902
NR_031729 FADS1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 "Cholesterol, HDL" rs174547 2.00E-12 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NR_031729 FADS1 20037589 http://www.ncbi.nlm.nih.gov/pubmed/20037589 Electrocardiography rs174547 7.00E-179 A genome-wide perspective of genetic variation in human metabolism. NHGRI|-1
NR_031729 FADS1 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Heart Rate rs174547 2.00E-09 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NR_031729 FADS1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs174547 2.00E-14 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NR_031729 FADS1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 "Lipoproteins, HDL" rs174548 1.00E-12 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NR_031729 FADS1 19043545 http://www.ncbi.nlm.nih.gov/pubmed/19043545 Phosphatidylcholines rs174548 5.00E-08 Genetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum. NHGRI|-1
NR_031729 FADS1 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs174548 5.00E-14 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NR_031729 FADS1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Tolerance Test rs174550 2.00E-15 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NR_031729 FADS1 20081858 http://www.ncbi.nlm.nih.gov/pubmed/20081858 Glucose Transporter Type 2 rs174550 5.00E-13 New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. NHGRI|-1
NR_033184 ZNF678 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Body Height rs1390401 5.00E-09 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NR_033289 GK5 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Kidney Diseases rs347685 3.00E-11 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NR_033290 FAM114A1 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs13150445 4.34E-07 NBL-GWAS version 1 dbGaP|2845
NR_033342 CELF5 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Nonalcoholic Fatty Liver Disease rs11669592 4.00E-06 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NR_033425 TSLP 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs3806932 3.00E-09 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NR_033488 BAT5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Psoriasis rs2295663 8.40E-24 "Genome Wide Association Study of Psoriasis (Pre-computed)" dbGaP|2855
NR_033659 STAT6 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Esophagitis rs167769 2.00E-06 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NR_033662 CSF3 20172861 http://www.ncbi.nlm.nih.gov/pubmed/20172861 Leukocyte Count rs4794822 6.00E-10 Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count. NHGRI|-1
NR_033662 CSF3 21738478 http://www.ncbi.nlm.nih.gov/pubmed/21738478 Neutrophils rs4794822 4.00E-16 Identification of nine novel Loci associated with white blood cell subtypes in a Japanese population. NHGRI|-1
NR_033716 SNX7 17068223 http://www.ncbi.nlm.nih.gov/pubmed/17068223 Inflammatory Bowel Diseases rs1351563 7.27E-05 A Genome-Wide Association Study on Inflammatory Bowel Disease dbGaP|2847
NR_033757 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 2.00E-11 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NR_033757 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 3.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NR_033757 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12138950 3.00E-18 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NR_033757 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs10917468 1.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NR_033758 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 2.00E-11 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NR_033758 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 3.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NR_033758 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12138950 3.00E-18 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NR_033758 C1orf151 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs10917468 1.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NR_033798 CAST 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4434401 6.76E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NR_033798 CAST 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs10053056 2.19E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NR_033798 CAST 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs27524 3.00E-11 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NR_033798 CAST 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs9918149 4.77E-05 " Whole Genome Association Study of Bipolar Disorder in the Population with African American ancestry (Pre-computed)" dbGaP|2863
NR_033799 NSF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs183211 1.05E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NR_033799 NSF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs169201 1.25E-07 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NR_033799 NSF 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson Disease rs199533 1.00E-14 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NR_033799 NSF 20711177 http://www.ncbi.nlm.nih.gov/pubmed/20711177 Parkinson Disease rs199533 1.00E-06 Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. NHGRI|-1
NR_033799 NSF 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs199533 5.05E-08 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NR_033815 ALS2CL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs7633016 3.19E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NR_033815 ALS2CL 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Leprosy rs4076927 2.53E-06 Genome-wide association study of leprosy in Chinese population dbGaP|2872
NR_033824 RXRG 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche rs466639 1.00E-13 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NR_033824 RXRG 21368711 http://www.ncbi.nlm.nih.gov/pubmed/21368711 Personality rs285480 4.00E-07 Genome-wide association study of personality traits in bipolar patients. NHGRI|-1
NR_033824 RXRG 19754311 http://www.ncbi.nlm.nih.gov/pubmed/19754311 Acquired Immunodeficiency Syndrome rs10800098 4.00E-06 Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). NHGRI|-1
NR_033971 RCN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs11031676 5.68E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NR_033971 RCN1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Depressive Disorder, Major" rs7944342 6.98E-05 "Genomewide Association in Population-Based Samples (Pre-computed)" dbGaP|2850
NR_034028 SLC6A13 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Creatinine rs10774021 1.00E-09 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NR_034053 TNPO3 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs12531711 9.00E-17 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NR_034053 TNPO3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs12531711 2.29E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NR_034053 TNPO3 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs12531711 6.00E-09 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NR_034053 TNPO3 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 "Arthritis, Rheumatoid" rs10488631 4.00E-11 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NR_034053 TNPO3 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 "Liver Cirrhosis, Biliary" rs10488631 2.00E-07 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NR_034053 TNPO3 20639880 http://www.ncbi.nlm.nih.gov/pubmed/20639880 "Liver Cirrhosis, Biliary" rs10488631 3.00E-10 Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis. NHGRI|-1
NR_034053 TNPO3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 1.65E-11 Whole Genome Association Study of Systemic Lupus Erythematosus dbGaP|2848
NR_034053 TNPO3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs10488631 2.48E-06 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NR_034053 TNPO3 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 "Lupus Erythematosus, Systemic" rs10488631 2.00E-11 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NR_034053 TNPO3 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 "Lupus Erythematosus, Systemic" rs10488631 7.00E-18 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NR_034053 TNPO3 20383147 http://www.ncbi.nlm.nih.gov/pubmed/20383147 "Scleroderma, Systemic" rs10488631 2.00E-13 Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. NHGRI|-1
NR_034053 TNPO3 21750679 http://www.ncbi.nlm.nih.gov/pubmed/21750679 Sclerosis rs10488631 4.00E-07 "Genome-Wide Scan Identifies TNIP1, PSORS1C1, and RHOB as Novel Risk Loci for Systemic Sclerosis" NHGRI|-1
NR_034164 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 2.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NR_034164 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NR_034165 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 2.75E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NR_034165 EXD2 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs11620883 5.75E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NR_036109 C9orf3 20932654 http://www.ncbi.nlm.nih.gov/pubmed/20932654 Erectile Dysfunction rs3802458 4.00E-06 Genome-wide association study to identify single nucleotide polymorphisms (SNPs) associated with the development of erectile dysfunction in African-American men after radiotherapy for prostate cancer. NHGRI|-1
NR_036125 MAML2 21658281 http://www.ncbi.nlm.nih.gov/pubmed/21658281 "Death, Sudden, Cardiac" rs10765792 8.00E-13 GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. NHGRI|-1
NR_036125 MAML2 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs7115578 8.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NR_036199 PLEKHM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11012 2.85E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NR_036199 PLEKHM1 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs11012 6.00E-08 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NR_036199 PLEKHM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11012 8.77E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NR_036255 AMOT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs547425 1.12E-04 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NR_036255 AMOT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alzheimer Disease rs648170 7.30E-05 Genotype-Phenotype Associations in Alzheimer’s disease dbGaP|2879
NR_036271 PLEKHM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11012 2.85E-06 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NR_036271 PLEKHM1 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson Disease rs11012 6.00E-08 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NR_036271 PLEKHM1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11012 8.77E-05 Genome Wide Association Study in Familial Parkinson Disease dbGaP|2865
NR_036441 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs1016771 1.26E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NR_036441 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2043890 1.53E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NR_036441 VRK2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Bipolar Disorder rs2717055 4.33E-05 "Genome Wide Association Study of Bipolar Disorder in the Population with European ancestry(Pre-computed)" dbGaP|2858
NR_036441 VRK2 19571808 http://www.ncbi.nlm.nih.gov/pubmed/19571808 Schizophrenia rs2312147 3.00E-07 Common variants conferring risk of schizophrenia. NHGRI|-1
NR_036448 DTNBP1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Stroke rs9296985 1.07E-04 Genome-wide association between genotype and incident stroke in African-American participants dbGaP|2887
NR_036514 C17orf62 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Insulin-Like Growth Factor I rs9303029 4.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NR_036516 C17orf62 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Insulin-Like Growth Factor I rs9303029 4.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NR_036517 C17orf62 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Insulin-Like Growth Factor I rs9303029 4.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NR_036542 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs729662 8.52E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NR_036542 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs7481584 9.54E-05 GWAS for alcohol dependence in European-Americans dbGaP|2892
NR_036542 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NR_036542 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 4.55E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NR_036542 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs739401 7.54E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NR_036542 CARS 20834067 http://www.ncbi.nlm.nih.gov/pubmed/20834067 Longevity rs739401 1.00E-06 Joint influence of small-effect genetic variants on human longevity. NHGRI|-1
NR_036542 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs438384 1.07E-04 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NR_036542 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 2.60E-05 "Genome wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2852
NR_036542 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 3.06E-06 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NR_036542 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs451041 9.80E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NR_036542 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs369461 2.50E-05 "GAIN-NIDDK: Genome-wide Association of Susceptibility Genes for Diabetic Nephropathy in Type 1 Diabetes (Pre-computed)" dbGaP|2866
NR_036542 CARS 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Diabetic Nephropathies rs369461 7.87E-05 Genome-wide association scan for diabetic nephropathy susceptibility genes in type 1 diabetes dbGaP|2864
NR_036576 APTX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10971259 1.34E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NR_036577 APTX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10971259 1.34E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NR_036578 APTX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10971259 1.34E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NR_036579 APTX 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs10971259 1.34E-04 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NR_036585 IRF4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Eye Color rs12203592 2.00E-15 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NR_036585 IRF4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12203592 2.00E-28 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NR_036585 IRF4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Hair Color rs12203592 4.00E-07 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NR_036585 IRF4 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs12203592 7.00E-127 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NR_036585 IRF4 18483556 http://www.ncbi.nlm.nih.gov/pubmed/18483556 Hair Color rs12203592 9.00E-28 A genome-wide association study identifies novel alleles associated with hair color and skin pigmentation. NHGRI|-1
NR_036585 IRF4 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Melanosis rs12203592 2.00E-91 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NR_036585 IRF4 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Neuroblastoma rs12203592 4.90E-05 NBL-GWAS version 2 dbGaP|2895
NR_036585 IRF4 21685912 http://www.ncbi.nlm.nih.gov/pubmed/21685912 "Supranuclear Palsy, Progressive" rs12203592 6.00E-15 Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy. NHGRI|-1
NR_036585 IRF4 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 "Leukemia, Lymphocytic, Chronic, B-Cell" rs872071 2.00E-20 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NR_036585 IRF4 21131588 http://www.ncbi.nlm.nih.gov/pubmed/21131588 "Leukemia, Lymphoid" rs9378805 2.00E-06 Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL. NHGRI|-1
NR_036585 IRF4 17952075 http://www.ncbi.nlm.nih.gov/pubmed/17952075 Melanosis rs1540771 4.00E-18 "Genetic determinants of hair, eye and skin pigmentation in Europeans." NHGRI|-1
NR_036585 IRF4 21700618 http://www.ncbi.nlm.nih.gov/pubmed/21700618 "Carcinoma, Basal Cell" rs12210050 1.00E-09 Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma. NHGRI|-1
NR_036585 IRF4 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Suntan rs12210050 5.00E-14 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NR_036585 IRF4 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs1033180 6.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NR_036614 DCLK2 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs2654831 8.63E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NR_036627 RBM5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Alcoholism rs2624834 4.44E-05 GWAS for alcohol dependence in African-Americans dbGaP|2891
NR_036634 TGFBR3 19249006 http://www.ncbi.nlm.nih.gov/pubmed/19249006 Bone Density rs17131547 1.00E-06 Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groups. NHGRI|-1
NR_036637 C1orf93 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs734999 3.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NR_036638 C1orf93 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs734999 3.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NR_036641 PDGFC 19786962 http://www.ncbi.nlm.nih.gov/pubmed/19786962 Speech Perception rs4234898 5.00E-08 First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. NHGRI|-1
NR_036682 BCL7B 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-Reactive Protein rs13233571 4.00E-09 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NR_036691 NFYC 21507922 http://www.ncbi.nlm.nih.gov/pubmed/21507922 Neutrophils rs4660456 4.00E-06 Duffy-null-associated low neutrophil counts influence HIV-1 susceptibility in high-risk South African black women. NHGRI|-1
NR_036693 CLEC2D 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 "Diabetes Mellitus, Type 1" rs3764021 5.00E-08 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NR_036752 NOL4 19846067 http://www.ncbi.nlm.nih.gov/pubmed/19846067 Citalopram rs7239368 9.00E-06 A genomewide association study of citalopram response in major depressive disorder. NHGRI|-1
NR_036752 NOL4 20360315 http://www.ncbi.nlm.nih.gov/pubmed/20360315 Antidepressive Agents rs1013696 4.00E-06 Genome-wide pharmacogenetics of antidepressant response in the GENDEP project. NHGRI|-1
NR_037150 CDKN1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs236449 9.40E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NR_037150 CDKN1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs236448 9.39E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NR_037150 CDKN1A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs1321311 3.00E-10 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NR_037150 CDKN1A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9470361 3.00E-27 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NR_037151 CDKN1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs236449 9.40E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NR_037151 CDKN1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs236448 9.39E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NR_037151 CDKN1A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs1321311 3.00E-10 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NR_037151 CDKN1A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9470361 3.00E-27 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NR_037152 CDKN1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs236449 9.40E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NR_037152 CDKN1A 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs236448 9.39E-05 A genome-wide association study identifies alleles associated with risk of Pancreatic cancer dbGaP|2874
NR_037152 CDKN1A 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiography rs1321311 3.00E-10 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NR_037152 CDKN1A 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Heart Function Tests rs9470361 3.00E-27 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NR_037163 POU2F1 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Alkaline Phosphatase rs9803659 4.00E-06 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NR_037166 SOD2 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Ferritins rs4516970 1.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NR_037171 PRRT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7383258 1.51E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_037171 PRRT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9296009 1.19E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_037172 PRRT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs7383258 1.51E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_037172 PRRT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9296009 1.19E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_037431 UCK2 19483681 http://www.ncbi.nlm.nih.gov/pubmed/19483681 Testicular Neoplasms rs4657482 2.00E-06 A genome-wide association study of testicular germ cell tumor. NHGRI|-1
NR_037465 PLCL2 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs1372072 2.00E-08 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NR_037482 SYTL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9364496 1.79E-11 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NR_037482 SYTL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs6455600 1.19E-07 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NR_037482 SYTL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs2129209 2.62E-08 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NR_037482 SYTL3 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Lipoprotein(a) rs9456350 2.32E-10 Genome-Wide Association Study of Plasma Lp(a) Levels dbGaP|2870
NR_037638 SLC28A3 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 "Cholesterol, HDL" rs10123041 6.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NR_037644 AS3MT 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Parkinson Disease rs11191425 3.96E-05 Genome-wide Association of Parkinson Disease in Samples Sharing Common Caucasian Ancestry dbGaP|2868
NR_037660 POC1B 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Pancreatic Neoplasms rs770374 5.30E-05 " Dichotomous (Pancreatic cancer cases vs. unaffected controls), trend, adjusted, CEU for PanScan I" dbGaP|2889
NR_037670 SNX10 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4563785 4.83E-06 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NR_037670 SNX10 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs4563785 6.51E-05 Genome-Wide Genotypic Association of Parkinson Disease in Additive model dbGaP|3
NR_037670 SNX10 17434096 http://www.ncbi.nlm.nih.gov/pubmed/17434096 Stroke rs4563785 3.60E-05 Genome-wide genotype associations in patients with ischaemic stroke dbGaP|2844
NR_037670 SNX10 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking rs886716 8.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NR_037687 PLXNC1 17052657 http://www.ncbi.nlm.nih.gov/pubmed/17052657 Parkinson Disease rs865569 8.93E-05 Genome-Wide Genotypic Association of Parkinson Disease dbGaP|4
NR_037791 EGLN2 20418890 http://www.ncbi.nlm.nih.gov/pubmed/20418890 Smoking rs3733829 1.00E-08 Genome-wide meta-analyses identify multiple loci associated with smoking behavior. NHGRI|-1
NR_037840 IL15 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs17007695 9.00E-07 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NR_037840 IL15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs746484 6.98E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NR_037840 IL15 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs9308140 5.26E-05 "Genome-Wide Allelic Association of AMD Status in Affy 100k Chip (Pre-computed)" dbGaP|2
NR_037840 IL15 18463370 http://www.ncbi.nlm.nih.gov/pubmed/18463370 Neuroblastoma rs4267812 6.73E-06 NBL-GWAS version 1 dbGaP|2845
NR_037846 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3749953 2.36E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_037846 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3131379 7.24E-85 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NR_037846 MSH5 18204446 http://www.ncbi.nlm.nih.gov/pubmed/18204446 "Lupus Erythematosus, Systemic" rs3131379 2.00E-52 "Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci." NHGRI|-1
NR_037846 MSH5 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Lupus Erythematosus, Systemic" rs3131379 4.89E-08 Genome-wide Association scan in women with systemic lupus erythematosus dbGaP|2867
NR_037852 BAT1 17660530 http://www.ncbi.nlm.nih.gov/pubmed/17660530 Multiple Sclerosis rs3115537 2.46E-13 Genome Wide Association Study of Multiple Sclerosis dbGaP|2854
NR_037852 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3093978 8.82E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_037852 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3093948 8.72E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_037852 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3093976 1.03E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_037852 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3130057 1.07E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_037852 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs2734583 5.29E-68 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NR_037852 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs3130058 6.23E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_037852 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2516393 8.82E-07 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_037852 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2239709 4.56E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_037852 BAT1 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs2251824 5.97E-06 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_037860 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3096697 2.16E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NR_037860 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3096697 5.66E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_037860 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130347 1.22E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_037860 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130347 3.62E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NR_037861 PPT2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 "Diabetes Mellitus, Type 1" rs3134603 3.36E-116 Genome-Wide Association Study in Type 1 Diabetes dbGaP|2862
NR_037861 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3096697 2.16E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NR_037861 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3096697 5.66E-06 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_037861 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130347 1.22E-05 Genome Wide Association Study in Age-related Macular Degeneration (AMD) using Logistic Regression Adjusting for First Two Principal Components dbGaP|2890
NR_037861 EGFL8 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Macular Degeneration rs3130347 3.62E-08 "CIDR: A Joint Genome Wide Association Study in Age related Macular Degeneration (AMD) (Pre-computed)" dbGaP|2869
NR_037882 RTEL1 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs6010620 2.00E-09 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NR_037882 RTEL1 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs6010620 3.00E-12 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NR_037882 RTEL1 19578366 http://www.ncbi.nlm.nih.gov/pubmed/19578366 Glioma rs6010620 3.00E-09 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. NHGRI|-1
NR_037882 RTEL1 19578366 http://www.ncbi.nlm.nih.gov/pubmed/19578366 Glioma rs4809324 2.00E-09 Variants in the CDKN2B and RTEL1 regions are associated with high-grade glioma susceptibility. NHGRI|-1
NR_037882 RTEL1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 "Colitis, Ulcerative" rs2297441 2.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NR_037910 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286411 2.12E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NR_037910 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 5.38E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NR_037910 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286405 6.67E-07 Genome-wide association study of HbA1C in combined group dbGaP|2882
NR_037910 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs169587 1.61E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NR_037910 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs1605683 1.20E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NR_037910 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs286388 1.39E-06 Genome-wide association study of HbA1C in combined group dbGaP|2882
NR_037910 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 1.29E-05 Genome-wide association study of HbA1C in combined group dbGaP|2882
NR_037910 PRLR 19875614 http://www.ncbi.nlm.nih.gov/pubmed/19875614 "Hemoglobin A, Glycosylated" rs10512623 3.17E-05 Genome-wide association study of HbA1C in conventional treatment group dbGaP|2880
NR_037947 NSUN2 0 http://www.ncbi.nlm.nih.gov/pubmed/0 Behcet Syndrome rs563624 6.12E-05 Genome-wide Association Study of Behçet’s Disease dbGaP|2888
NR_037951 C1QTNF3 11022011 http://www.ncbi.nlm.nih.gov/pubmed/11022011 Asthma rs10075914 7.33E-05 Genome-wide Association Study of YKL-40 Levels in the Hutterites dbGaP|2843
NR_037951 C1QTNF3 19454037 http://www.ncbi.nlm.nih.gov/pubmed/19454037 Hypertension rs409045 8.00E-07 Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: the HyperGEN Study. NHGRI|-1
NR_038121 ELMO1 17653210 http://www.ncbi.nlm.nih.gov/pubmed/17653210 Diabetic Nephropathies rs741301 8.00E-06 Genetic variations associated with diabetic nephropathy and type II diabetes in a Japanese population. NHGRI|-1
NR_038121 ELMO1 20031603 http://www.ncbi.nlm.nih.gov/pubmed/20031603 Heart Rate rs10488031 2.00E-06 A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project. NHGRI|-1
NR_038121 ELMO1 19176441 http://www.ncbi.nlm.nih.gov/pubmed/19176441 Precursor Cell Lymphoblastic Leukemia-Lymphoma rs4723619 3.00E-06 Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia. NHGRI|-1
NR_038121 ELMO1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac Disease rs6974491 2.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NR_038121 ELMO1 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 "Liver Cirrhosis, Biliary" rs6974491 4.00E-08 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NR_038121 ELMO1 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Autoimmune Diseases rs11984075 5.00E-08 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NR_038125 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 2.00E-11 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NR_038125 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12045440 3.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NR_038125 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs12138950 3.00E-18 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NR_038125 CAPZB 21565293 http://www.ncbi.nlm.nih.gov/pubmed/21565293 Goiter rs10917468 1.00E-14 Genome-wide association study identifies four genetic loci associated with thyroid volume and goiter risk. NHGRI|-1
NR_038167 FUT8 20585324 http://www.ncbi.nlm.nih.gov/pubmed/20585324 Conduct Disorder rs1256531 4.00E-06 Genome-wide association study of conduct disorder symptomatology. NHGRI|-1
NM_000545 HNF1A 21647738 http://www.ncbi.nlm.nih.gov/pubmed/21647738 C-reactive protein rs7305618 1.00E-08 Genome-wide Association with C-Reactive Protein Levels in CLHNS: Evidence for the CRP and HNF1A Loci and their Interaction with Exposure to a Pathogenic Environment. NHGRI|-1
NM_018401 STK32B 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Coronary heart disease rs7697839 2.00E-11 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_018401 STK32B 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Coronary heart disease rs7673097 2.00E-11 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NR_037425 HSP90B1 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Coronary heart disease rs1165668 3.00E-09 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NR_037425 HSP90B1 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Coronary heart disease rs1165669 3.00E-09 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_004936 CDKN2B 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Coronary heart disease rs1333048 7.00E-14 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_004936 CDKN2B 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Coronary heart disease rs1333049 7.00E-14 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_000077 CDKN2A 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Coronary heart disease rs1333048 7.00E-14 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_000077 CDKN2A 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Coronary heart disease rs1333049 7.00E-14 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_001174158 ZFAT 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Hypertension rs7827545 2.00E-44 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_001174158 ZFAT 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Hypertension rs1372662 2.00E-44 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_002514 NOV 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Hypertension rs2469997 3.00E-16 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_002514 NOV 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Hypertension rs6469823 3.00E-16 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_004999 MYO6 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Hypertension rs3798440 3.00E-10 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_004999 MYO6 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Hypertension rs9350602 3.00E-10 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_145000 RANBP3L 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Hypertension rs7735940 5.00E-13 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_145000 RANBP3L 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Hypertension rs12522034 5.00E-13 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_022406 XRCC4 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Hypertension rs6452524 2.00E-07 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_022406 XRCC4 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Hypertension rs6887846 2.00E-07 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_001508 GPR39 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Hypertension rs13420028 1.00E-10 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_001508 GPR39 21626137 http://www.ncbi.nlm.nih.gov/pubmed/21626137 Hypertension rs10188442 1.00E-10 Two-marker association tests yield new disease associations for coronary artery disease and hypertension. NHGRI|-1
NM_002451 MTAP 21606135 http://www.ncbi.nlm.nih.gov/pubmed/21606135 Coronary heart disease rs7865618 2.00E-27 A Genome-wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease. NHGRI|-1
NM_012153 EHF 21602797 http://www.ncbi.nlm.nih.gov/pubmed/21602797 Cystic fibrosis severity rs12793173 1.00E-09 Genome-wide association and linkage identify modifier loci of lung disease severity in cystic fibrosis at 11p13 and 20q13.2. NHGRI|-1
NM_000545 HNF1A 21573907 http://www.ncbi.nlm.nih.gov/pubmed/21573907 Type 2 diabetes rs7305618 2.00E-08 "Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas." NHGRI|-1
NM_000077 CDKN2A 21573907 http://www.ncbi.nlm.nih.gov/pubmed/21573907 Type 2 diabetes rs1333051 6.00E-10 "Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas." NHGRI|-1
NM_004936 CDKN2B 21573907 http://www.ncbi.nlm.nih.gov/pubmed/21573907 Type 2 diabetes rs1333051 6.00E-10 "Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas." NHGRI|-1
NR_024096 C14ORF70 21573907 http://www.ncbi.nlm.nih.gov/pubmed/21573907 Type 2 diabetes rs730570 8.00E-06 "Genome-wide association study of type 2 diabetes in a sample from Mexico City and a meta-analysis of a Mexican-American sample from Starr County, Texas." NHGRI|-1
NM_002150 HPD 21572414 http://www.ncbi.nlm.nih.gov/pubmed/21572414 Urinary metabolites rs830124 1.00E-46 A genome-wide association study of metabolic traits in human urine. NHGRI|-1
NM_173827 COX18 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 Dialysis-related mortality rs6816344 1.00E-06 Genome-Wide Association Scan for Survival on Dialysis in African-Americans with Type 2 Diabetes. NHGRI|-1
NM_007038 ADAMTS5 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 Dialysis-related mortality rs1452093 2.00E-06 Genome-Wide Association Scan for Survival on Dialysis in African-Americans with Type 2 Diabetes. NHGRI|-1
NM_007038 ADAMTS5 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 Dialysis-related mortality rs9977499 4.00E-06 Genome-Wide Association Scan for Survival on Dialysis in African-Americans with Type 2 Diabetes. NHGRI|-1
NM_005853 IRX5 21546767 http://www.ncbi.nlm.nih.gov/pubmed/21546767 Dialysis-related mortality rs9921518 9.00E-06 Genome-Wide Association Scan for Survival on Dialysis in African-Americans with Type 2 Diabetes. NHGRI|-1
NM_015440 MTHFD1L 21540461 http://www.ncbi.nlm.nih.gov/pubmed/21540461 Chronic myeloid leukemia rs4869742 2.00E-06 A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia. NHGRI|-1
NM_144497 AKAP12 21540461 http://www.ncbi.nlm.nih.gov/pubmed/21540461 Chronic myeloid leukemia rs4869742 2.00E-06 A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia. NHGRI|-1
NM_020861 ZBTB2 21540461 http://www.ncbi.nlm.nih.gov/pubmed/21540461 Chronic myeloid leukemia rs4869742 2.00E-06 A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia. NHGRI|-1
NM_017909 RMND1 21540461 http://www.ncbi.nlm.nih.gov/pubmed/21540461 Chronic myeloid leukemia rs4869742 2.00E-06 A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia. NHGRI|-1
NM_001122740 ESR1 21540461 http://www.ncbi.nlm.nih.gov/pubmed/21540461 Chronic myeloid leukemia rs4869742 2.00E-06 A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia. NHGRI|-1
NM_015626 WSB1 21540461 http://www.ncbi.nlm.nih.gov/pubmed/21540461 Chronic myeloid leukemia rs4795519 1.00E-12 A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia. NHGRI|-1
NR_028336 FAM27L 21540461 http://www.ncbi.nlm.nih.gov/pubmed/21540461 Chronic myeloid leukemia rs4795519 1.00E-12 A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia. NHGRI|-1
NM_000077 CDKN2A 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs2157719 5.00E-16 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_004936 CDKN2B 21531791 http://www.ncbi.nlm.nih.gov/pubmed/21531791 Glioma rs2157719 5.00E-16 Chromosome 7p11.2 (EGFR) variation influences glioma risk. NHGRI|-1
NM_012399 PITPNB 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs5762430 7.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_177924 ASAH1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 8.00E-08 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_182678 UBE2E3 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs16867321 2.00E-06 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_177924 ASAH1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 2.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_177924 ASAH1 21552555 http://www.ncbi.nlm.nih.gov/pubmed/21552555 Obesity rs17126232 4.00E-07 A genome-wide association study on obesity and obesity-related traits. NHGRI|-1
NM_005577 LPA 21493818 http://www.ncbi.nlm.nih.gov/pubmed/21493818 Monocyte early outgrowth colony forming units rs402219 6.00E-07 Genetic and clinical correlates of early-outgrowth colony-forming units. NHGRI|-1
NM_002626 PFKL 21505073 http://www.ncbi.nlm.nih.gov/pubmed/21505073 Rheumatoid arthritis rs2075876 4.00E-09 The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population. NHGRI|-1
NM_002122 HLA-DQA1 21502966 http://www.ncbi.nlm.nih.gov/pubmed/21502966 Response to interferon beta therapy rs9272105 4.00E-10 Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients. NHGRI|-1
NM_002124 HLA-DRB1 21502966 http://www.ncbi.nlm.nih.gov/pubmed/21502966 Response to interferon beta therapy rs9272105 4.00E-10 Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients. NHGRI|-1
NM_014957 DENND3 21502966 http://www.ncbi.nlm.nih.gov/pubmed/21502966 Response to interferon beta therapy rs4961252 3.00E-08 Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients. NHGRI|-1
NM_153831 PTK2 21502966 http://www.ncbi.nlm.nih.gov/pubmed/21502966 Response to interferon beta therapy rs4961252 3.00E-08 Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients. NHGRI|-1
NM_001177519 MICA 21499248 http://www.ncbi.nlm.nih.gov/pubmed/21499248 Hepatocellular carcinoma rs2596542 4.00E-13 Genome-wide association study identifies a susceptibility locus for HCV-induced hepatocellular carcinoma. NHGRI|-1
NM_002116 HLA-A 21570397 http://www.ncbi.nlm.nih.gov/pubmed/21570397 Drug-induced liver injury (amoxicillin-clavulanate) rs2523822 2.00E-10 Susceptibility to Amoxicillin-Clavulanate-Induced Liver Injury Is Influenced by Multiple HLA Class I and II Alleles. NHGRI|-1
NM_138787 C11ORF74 21478494 http://www.ncbi.nlm.nih.gov/pubmed/21478494 Cutaneous nevi rs16930685 2.00E-06 Genome-wide association study identifies nidogen 1 (NID1) as a susceptibility locus to cutaneous nevi and melanoma risk. NHGRI|-1
NM_153371 LNX2 21471979 http://www.ncbi.nlm.nih.gov/pubmed/21471979 Large B-cell lymphoma rs7097 7.00E-06 Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility. NHGRI|-1
NM_021932 RIC8A 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs2280543 4.00E-12 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_001017524 SIRT3 21460842 http://www.ncbi.nlm.nih.gov/pubmed/21460842 Uterine fibroids rs2280543 4.00E-12 A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids. NHGRI|-1
NM_002269 KPNA5 21460395 http://www.ncbi.nlm.nih.gov/pubmed/21460395 Telomere length rs654128 3.00E-06 A genome-wide association study identifies a locus on chromosome 14q21 as a predictor of leukocyte telomere length and as a marker of susceptibility for bladder cancer. NHGRI|-1
NM_002124 HLA-DRB1 21452313 http://www.ncbi.nlm.nih.gov/pubmed/21452313 Rheumatoid arthritis rs7765379 5.00E-23 Genome-wide association study of rheumatoid arthritis in Koreans: population-specific loci as well as overlap with European susceptibility loci. NHGRI|-1
NM_001143829 CCDC68 21441570 http://www.ncbi.nlm.nih.gov/pubmed/21441570 Diabetic retinopathy rs1970671 3.00E-06 Genome-wide meta-analysis for severe diabetic retinopathy. NHGRI|-1
NM_139076 FAM175A 21437268 http://www.ncbi.nlm.nih.gov/pubmed/21437268 Upper aerodigestive tract cancers rs1494961 1.00E-08 A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. NHGRI|-1
NM_000690 ALDH2 21437268 http://www.ncbi.nlm.nih.gov/pubmed/21437268 Upper aerodigestive tract cancers rs4767364 2.00E-08 A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium. NHGRI|-1
NM_002124 HLA-DRB1 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 Nephropathy rs9275596 2.00E-26 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_002122 HLA-DQA1 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 Nephropathy rs9275596 2.00E-26 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_033554 HLA-DPA1 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 Nephropathy rs1883414 5.00E-09 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_002121 HLA-DPB1 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 Nephropathy rs1883414 5.00E-09 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_021090 MTMR3 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 Nephropathy rs2412971 2.00E-09 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_002309 LIF 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 Nephropathy rs2412971 2.00E-09 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_020530 OSM 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 Nephropathy rs2412971 2.00E-09 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_018833 TAP2 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 Nephropathy rs9357155 2.00E-12 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_000593 TAP1 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 Nephropathy rs9357155 2.00E-12 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_002800 PSMB9 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 Nephropathy rs9357155 2.00E-12 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_021023 CFHR3 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 Nephropathy rs6677604 3.00E-10 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_030787 CFHR5 21399633 http://www.ncbi.nlm.nih.gov/pubmed/21399633 Nephropathy rs6677604 3.00E-10 Genome-wide association study identifies susceptibility loci for IgA nephropathy. NHGRI|-1
NM_139280 ORMDL3 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 Primary biliary cirrhosis rs7208487 8.00E-07 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_001195215 DENND1B 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 Primary biliary cirrhosis rs12134279 2.00E-14 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_006291 TNFAIP2 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 Primary biliary cirrhosis rs8017161 3.00E-13 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_003151 STAT4 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 Primary biliary cirrhosis rs10931468 2.00E-19 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_002185 IL7R 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 Primary biliary cirrhosis rs860413 1.00E-11 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_005191 CD80 21399635 http://www.ncbi.nlm.nih.gov/pubmed/21399635 Primary biliary cirrhosis rs2293370 3.00E-11 Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis. NHGRI|-1
NM_000102 CYP17A1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs12413409 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001134373 NT5C2 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs12413409 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_021947 SRR 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs216172 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_007241 SNF8 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs46522 2.00E-08 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_032476 MRPS6 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs9982601 4.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001195799 LDLR 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs1122608 1.00E-09 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_000077 CDKN2A 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs4977574 1.00E-22 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_004936 CDKN2B 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs4977574 1.00E-22 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_016084 RASD1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs12936587 4.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001166598 APOA5 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs964184 1.00E-17 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_000482 APOA4 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs964184 1.00E-17 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_000040 APOC3 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs964184 1.00E-17 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_000039 APOA1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs964184 1.00E-17 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_002959 SORT1 21378990 http://www.ncbi.nlm.nih.gov/pubmed/21378990 Coronary heart disease rs599839 3.00E-10 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. NHGRI|-1
NM_001005290 PSRC1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary heart disease rs646776 6.00E-10 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_002959 SORT1 21378988 http://www.ncbi.nlm.nih.gov/pubmed/21378988 Coronary heart disease rs646776 6.00E-10 A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease. NHGRI|-1
NM_020056 HLA-DQA2 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 Systemic lupus erythematosus rs2301271 2.00E-12 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_002122 HLA-DQA1 21408207 http://www.ncbi.nlm.nih.gov/pubmed/21408207 Systemic lupus erythematosus rs2647012 8.00E-06 Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. NHGRI|-1
NM_006768 BRAP 21372407 http://www.ncbi.nlm.nih.gov/pubmed/21372407 Drinking behavior rs671 4.00E-211 Confirmation of ALDH2 as a Major locus of drinking behavior and of its variants regulating multiple metabolic phenotypes in a Japanese population. NHGRI|-1
NM_012425 RSU1 21355061 http://www.ncbi.nlm.nih.gov/pubmed/21355061 Urinary albumin excretion rs1801239 1.00E-11 CUBN is a gene locus for albuminuria. NHGRI|-1
NM_005658 TRAF1 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Celiac disease and Rheumatoid arthritis rs1953126 4.00E-11 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NR_028437 UBE2L3 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Celiac disease and Rheumatoid arthritis rs2298428 3.00E-10 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_000075 CDK4 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Celiac disease and Rheumatoid arthritis rs10876993 4.00E-06 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_024669 ANKRD55 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Celiac disease and Rheumatoid arthritis rs1020388 3.00E-07 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_005475 SH2B3 21383967 http://www.ncbi.nlm.nih.gov/pubmed/21383967 Celiac disease and Rheumatoid arthritis rs653178 3.00E-19 Meta-analysis of genome-wide association studies in celiac disease and rheumatoid arthritis identifies fourteen non-HLA shared loci. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs10189857 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs6545816 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs6545817 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs1427407 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs7599488 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs1896294 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs766432 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs11886868 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs10195871 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs10172646 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs4671393 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs7584113 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs7557939 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs6706648 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs6738440 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs7565301 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs6729815 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs1896295 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs1896296 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs7606173 2.00E-07 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs10189857 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs6545816 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs6545817 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs1427407 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs7599488 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs1896294 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs766432 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs11886868 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs10195871 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs10172646 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs4671393 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs7584113 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs7557939 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs6706648 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs6738440 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs7565301 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs6729815 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs1896295 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs1896296 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_018014 BCL11A 21326311 http://www.ncbi.nlm.nih.gov/pubmed/21326311 F-cell distribution rs7606173 2.00E-16 Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients. NHGRI|-1
NM_006781 C6ORF10 21326295 http://www.ncbi.nlm.nih.gov/pubmed/21326295 Vitiligo rs7758128 8.00E-11 Genome-Wide Analysis Identifies a Quantitative Trait Locus in the MHC Class II Region Associated with Generalized Vitiligo Age of Onset. NHGRI|-1
NM_182488 USP12 21314694 http://www.ncbi.nlm.nih.gov/pubmed/21314694 Alcohol dependence rs12020569 5.00E-06 Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample. NHGRI|-1
NM_005288 GPR12 21314694 http://www.ncbi.nlm.nih.gov/pubmed/21314694 Alcohol dependence rs12020569 5.00E-06 Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample. NHGRI|-1
NM_138807 C3ORF31 21314694 http://www.ncbi.nlm.nih.gov/pubmed/21314694 Alcohol dependence rs6777876 4.00E-07 Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample. NHGRI|-1
NM_000078 CETP 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary heart disease rs16965039 6.00E-07 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_021194 SLC30A1 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary heart disease rs7526425 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_183059 RD3 21347282 http://www.ncbi.nlm.nih.gov/pubmed/21347282 Coronary heart disease rs7526425 1.00E-06 "Genome-wide association study of coronary heart disease and its risk factors in 8,090 African Americans: the NHLBI CARe Project." NHGRI|-1
NM_001134419 CDC7 21307088 http://www.ncbi.nlm.nih.gov/pubmed/21307088 Optic disc parameters rs1192415 8.00E-17 "Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area." NHGRI|-1
NM_001195684 TGFBR3 21307088 http://www.ncbi.nlm.nih.gov/pubmed/21307088 Optic disc parameters rs1192415 8.00E-17 "Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area." NHGRI|-1
NM_001135653 PABPC4 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-reactive protein rs12037222 6.00E-11 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_002303 LEPR 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-reactive protein rs4420065 4.00E-62 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_003720 PSMG1 21300955 http://www.ncbi.nlm.nih.gov/pubmed/21300955 C-reactive protein rs2836878 2.00E-07 Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels. NHGRI|-1
NM_001244 TNFSF8 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs4246905 6.00E-12 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_019892 INPP5E 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs10781499 3.00E-19 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_006643 SDCCAG3 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs10781499 3.00E-19 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_014866 SEC16A 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs10781499 3.00E-19 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_003086 SNAPC4 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs10781499 3.00E-19 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_153758 IL19 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs3024505 6.00E-17 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001002274 FCGR2B 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs1801274 2.00E-20 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_002155 HSPA6 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs1801274 2.00E-20 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_002122 HLA-DQA1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs9268853 1.00E-55 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_002124 HLA-DRB1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs9268853 1.00E-55 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_019111 HLA-DRA 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs9268853 1.00E-55 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_019602 BTNL2 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs9268853 1.00E-55 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_012481 IKZF3 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs2872507 5.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_139280 ORMDL3 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs2872507 5.00E-11 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001001852 PIM3 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs5771069 2.00E-07 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001561 TNFRSF9 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs35675666 5.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_006786 UTS2 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs35675666 5.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_020998 MST1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs9822268 2.00E-17 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_003335 UBA7 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs9822268 2.00E-17 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_198722 AMIGO3 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs9822268 2.00E-17 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_021971 GMPPB 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs9822268 2.00E-17 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_003458 BSN 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs9822268 2.00E-17 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_021803 IL21 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs17388568 9.00E-07 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_018402 IL26 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs7134599 1.00E-16 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_014638 PLCH2 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs734999 3.00E-09 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_000578 SLC11A1 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs11676348 1.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_001087 AAMP 21297633 http://www.ncbi.nlm.nih.gov/pubmed/21297633 Ulcerative colitis rs11676348 1.00E-10 "Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47." NHGRI|-1
NM_016841 MAPT 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson's disease rs2942168 1.00E-28 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_152280 SYT11 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson's disease rs34372695 4.00E-12 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_004334 BST1 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson's disease rs11724635 1.00E-16 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_005255 GAK 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson's disease rs6599388 4.00E-12 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_003959 HIP1R 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson's disease rs12817488 3.00E-13 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_002125 HLA-DRB5 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson's disease NR 2.00E-14 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_013233 STK39 21292315 http://www.ncbi.nlm.nih.gov/pubmed/21292315 Parkinson's disease rs2102808 4.00E-10 Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies. NHGRI|-1
NM_018189 DPPA4 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiac hypertrophy rs769554 3.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_006355 TRIM38 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiac hypertrophy rs10947055 2.00E-07 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_003107 SOX4 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiac hypertrophy rs4236016 4.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_178539 FAM19A2 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiac hypertrophy rs10506410 2.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_001165947 HTR2A 21348951 http://www.ncbi.nlm.nih.gov/pubmed/21348951 Cardiac hypertrophy rs1575891 6.00E-06 Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. NHGRI|-1
NM_014577 BRD1 21273288 http://www.ncbi.nlm.nih.gov/pubmed/21273288 Natriuretic peptide levels rs6009824 7.00E-06 Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. NHGRI|-1
NR_026997 C22ORF34 21273288 http://www.ncbi.nlm.nih.gov/pubmed/21273288 Natriuretic peptide levels rs6009824 7.00E-06 Genome-wide association analysis and fine mapping of NT-proBNP level provide novel insight into the role of the MTHFR-CLCN6-NPPA-NPPB gene cluster. NHGRI|-1
NM_001122740 ESR1 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast cancer rs3734805 1.00E-07 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_000141 FGFR2 21263130 http://www.ncbi.nlm.nih.gov/pubmed/21263130 Breast cancer rs10510102 2.00E-06 Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. NHGRI|-1
NM_002185 IL7R 21244703 http://www.ncbi.nlm.nih.gov/pubmed/21244703 Multiple sclerosis rs931555 4.00E-07 Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data. NHGRI|-1
NM_006725 CD6 21244703 http://www.ncbi.nlm.nih.gov/pubmed/21244703 Multiple sclerosis rs4939490 1.00E-09 Modeling the cumulative genetic risk for multiple sclerosis from genome-wide association data. NHGRI|-1
NM_021080 DAB1 21221998 http://www.ncbi.nlm.nih.gov/pubmed/21221998 Kawasaki disease rs527409 1.00E-06 A genome-wide association analysis reveals 1p31 and 2p13.3 as susceptibility loci for Kawasaki disease. NHGRI|-1
NR_027389 IGFALS 21216879 http://www.ncbi.nlm.nih.gov/pubmed/21216879 Insulin-like growth factors rs1065656 1.00E-11 A genome-wide association study identifies novel loci associated with circulating IGF-I and IGFBP-3. NHGRI|-1
NM_006614 CHL1 21216876 http://www.ncbi.nlm.nih.gov/pubmed/21216876 Scoliosis rs10510181 8.00E-07 Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genes. NHGRI|-1
NM_000051 ATM 21186350 http://www.ncbi.nlm.nih.gov/pubmed/21186350 Response to metformin rs11212617 3.00E-09 Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes. NHGRI|-1
NM_001040701 FUT6 21203500 http://www.ncbi.nlm.nih.gov/pubmed/21203500 N-glycan levels rs3760776 4.00E-17 Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation. NHGRI|-1
NM_001040701 FUT6 21203500 http://www.ncbi.nlm.nih.gov/pubmed/21203500 N-glycan levels rs3760776 9.00E-10 Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation. NHGRI|-1
NM_178156 FUT8 21203500 http://www.ncbi.nlm.nih.gov/pubmed/21203500 N-glycan levels rs10483776 1.00E-08 Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation. NHGRI|-1
NM_178156 FUT8 21203500 http://www.ncbi.nlm.nih.gov/pubmed/21203500 N-glycan levels rs7159888 3.00E-18 Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation. NHGRI|-1
NM_000545 HNF1A 21203500 http://www.ncbi.nlm.nih.gov/pubmed/21203500 N-glycan levels rs735396 4.00E-08 Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation. NHGRI|-1
NM_001040701 FUT6 21203500 http://www.ncbi.nlm.nih.gov/pubmed/21203500 N-glycan levels rs3760776 3.00E-12 Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation. NHGRI|-1
NM_001040701 FUT6 21203500 http://www.ncbi.nlm.nih.gov/pubmed/21203500 N-glycan levels rs3760776 1.00E-12 Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation. NHGRI|-1
NM_198253 TERT 21160077 http://www.ncbi.nlm.nih.gov/pubmed/21160077 Serum prostate-specific antigen levels rs401681 1.00E-10 Genetic correction of PSA values using sequence variants associated with PSA levels. NHGRI|-1
NM_139011 HFE 21149283 http://www.ncbi.nlm.nih.gov/pubmed/21149283 Serum markers of iron status rs17342717 9.00E-10 Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. NHGRI|-1
NM_139011 HFE 21149283 http://www.ncbi.nlm.nih.gov/pubmed/21149283 Serum markers of iron status rs1408272 9.00E-09 Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels. NHGRI|-1
NM_002116 HLA-A 21149285 http://www.ncbi.nlm.nih.gov/pubmed/21149285 Adverse response to carbamapezine NR 1.00E-16 Genome-wide association study identifies HLA-A*3101 allele as a genetic risk factor for carbamazepine-induced cutaneous adverse drug reactions in Japanese population. NHGRI|-1
NM_003483 HMGA2 21150874 http://www.ncbi.nlm.nih.gov/pubmed/21150874 Diabetic nephropathy rs2358944 4.00E-06 A genome-wide association study for diabetic nephropathy genes in African Americans. NHGRI|-1
NM_017774 CDKAL1 21139019 http://www.ncbi.nlm.nih.gov/pubmed/21139019 Ileal carcinoids rs2206734 8.00E-06 A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum. NHGRI|-1
NM_002125 HLA-DRB5 21131588 http://www.ncbi.nlm.nih.gov/pubmed/21131588 Chronic lymphocytic leukemia rs674313 7.00E-09 Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL. NHGRI|-1
NM_182577 ODF3L2 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger disorder rs892055 5.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_001012761 RGMB 21182207 http://www.ncbi.nlm.nih.gov/pubmed/21182207 Asperger disorder rs4703129 1.00E-06 Variants in several genomic regions associated with asperger disorder. NHGRI|-1
NM_032242 PLXNA1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 MRI atrophy measures rs9871760 4.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_182962 BIRC3 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 MRI atrophy measures rs2852894 1.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_175607 CNTN4 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Total ventricular volume rs10510217 3.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_006237 POU4F1 21116278 http://www.ncbi.nlm.nih.gov/pubmed/21116278 Total ventricular volume rs9574199 7.00E-06 Genome-wide association with MRI atrophy measures as a quantitative trait locus for Alzheimer's disease. NHGRI|-1
NM_004454 ETV5 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche (age at onset) rs2002675 1.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NR_027317 C3ORF65 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche (age at onset) rs2002675 1.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_014048 MKL2 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche (age at onset) rs1659127 4.00E-09 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_018112 TMEM38B 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche (age at onset) rs2090409 2.00E-33 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_001031712 TRMT11 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche (age at onset) rs1361108 2.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_145735 ARHGEF7 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche (age at onset) rs9555810 6.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NR_037804 NPHP3 21102462 http://www.ncbi.nlm.nih.gov/pubmed/21102462 Menarche (age at onset) rs6439371 1.00E-08 Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. NHGRI|-1
NM_000581 GPX1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs3197999 6.00E-17 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_003458 BSN 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs3197999 6.00E-17 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_005698 SCAMP3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs3180018 2.00E-13 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001018016 MUC1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs3180018 2.00E-13 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_004451 ESRRA 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs694739 6.00E-10 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001201402 GALC 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs8005161 4.00E-18 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_145659 IL27 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs151181 2.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001145795 SH2B1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs151181 2.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001014989 LAT 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs151181 2.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001770 CD19 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs151181 2.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_017805 RASIP1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs281379 7.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001244 TNFSF8 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs3810936 1.00E-15 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_003086 SNAPC4 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs4077515 1.00E-36 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_013402 FADS1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs102275 2.00E-11 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_153758 IL19 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs3024505 2.00E-14 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_003059 SLC22A4 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs12521868 1.00E-20 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_003060 SLC22A5 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs12521868 1.00E-20 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_002198 IRF1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs12521868 1.00E-20 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_000588 IL3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs12521868 1.00E-20 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_000201 ICAM1 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs12720356 1.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001017964 YDJC 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs181359 5.00E-16 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_021090 MTMR3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs713875 7.00E-12 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_004781 VAMP3 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs2797685 7.00E-09 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_198578 LRRK2 21102463 http://www.ncbi.nlm.nih.gov/pubmed/21102463 Crohn's disease rs11564258 6.00E-21 Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci. NHGRI|-1
NM_001142307 GTF2H1 21124955 http://www.ncbi.nlm.nih.gov/pubmed/21124955 Amyloid A Levels rs4353250 2.00E-51 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. NHGRI|-1
NM_017448 LDHC 21124955 http://www.ncbi.nlm.nih.gov/pubmed/21124955 Amyloid A Levels rs2896526 4.00E-22 Genome-wide association study identifies two novel regions at 11p15.5-p13 and 1p31 with major impact on acute-phase serum amyloid A. NHGRI|-1
NM_004334 BST1 21084426 http://www.ncbi.nlm.nih.gov/pubmed/21084426 Parkinson's disease rs4698412 2.00E-06 Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population. NHGRI|-1
NM_003162 STRN 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Ventricular conduction rs17020136 2.00E-09 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_212539 PRKCD 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Ventricular conduction rs4687718 6.00E-09 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_001128840 CACNA1D 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Ventricular conduction rs4687718 6.00E-09 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_012242 DKK1 21076409 http://www.ncbi.nlm.nih.gov/pubmed/21076409 Ventricular conduction rs1733724 3.00E-08 Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. NHGRI|-1
NM_000384 APOB 21059979 http://www.ncbi.nlm.nih.gov/pubmed/21059979 LDL cholesterol rs4971516 2.00E-52 Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish. NHGRI|-1
NM_000384 APOB 21059979 http://www.ncbi.nlm.nih.gov/pubmed/21059979 LDL cholesterol rs4971516 2.00E-40 Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amish. NHGRI|-1
NM_001177519 MICA 21051598 http://www.ncbi.nlm.nih.gov/pubmed/21051598 HIV-1 control rs4418214 1.00E-34 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. NHGRI|-1
NM_002117 HLA-C 21051598 http://www.ncbi.nlm.nih.gov/pubmed/21051598 HIV-1 control rs9264942 3.00E-35 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. NHGRI|-1
NM_005514 HLA-B 21051598 http://www.ncbi.nlm.nih.gov/pubmed/21051598 HIV-1 control rs2395029 1.00E-25 The major genetic determinants of HIV-1 control affect HLA class I peptide presentation. NHGRI|-1
NM_002908 REL 21037568 http://www.ncbi.nlm.nih.gov/pubmed/21037568 Hodgkin's lymphoma rs1432295 2.00E-08 "A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)." NHGRI|-1
NM_019111 HLA-DRA 21037568 http://www.ncbi.nlm.nih.gov/pubmed/21037568 Hodgkin's lymphoma rs6903608 3.00E-50 "A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)." NHGRI|-1
NM_014171 CRIPT 20966902 http://www.ncbi.nlm.nih.gov/pubmed/20966902 Height rs17818399 3.00E-07 Genome-wide association study of anthropometric traits and evidence of interactions with age and study year in Filipino women. NHGRI|-1
NM_002117 HLA-C 20953188 http://www.ncbi.nlm.nih.gov/pubmed/20953188 Psoriasis rs12191877 4.00E-32 Genome-wide association study identifies a psoriasis susceptibility locus at TRAF3IP2. NHGRI|-1
NM_001164281 TRAF3IP2 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs240993 5.00E-20 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_022168 IFIH1 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs17716942 1.00E-13 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_002117 HLA-C 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs10484554 4.00E-214 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_020529 NFKBIA 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs8016947 2.00E-11 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_001164281 TRAF3IP2 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs458017 2.00E-16 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_001164281 TRAF3IP2 20953190 http://www.ncbi.nlm.nih.gov/pubmed/20953190 Psoriasis rs465969 2.00E-16 A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1. NHGRI|-1
NM_020529 NFKBIA 20953189 http://www.ncbi.nlm.nih.gov/pubmed/20953189 Psoriasis rs12586317 2.00E-08 Genome-wide association analysis identifies three psoriasis susceptibility loci. NHGRI|-1
NM_030751 ZEB1 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-hip ratio rs7081678 6.00E-06 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_201263 WARS2 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-hip ratio rs984222 9.00E-25 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_153747 PIGC 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-hip ratio rs1011731 1.00E-17 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_032045 KREMEN1 20935629 http://www.ncbi.nlm.nih.gov/pubmed/20935629 Waist-hip ratio rs4823006 3.00E-11 Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. NHGRI|-1
NM_012306 FAIM2 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs7138803 2.00E-17 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_000164 GIPR 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs2287019 2.00E-16 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_018062 FANCL 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs887912 2.00E-12 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_018557 LRP1B 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs2890652 1.00E-10 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_145902 HMGA1 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs206936 3.00E-08 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_177528 SULT1A2 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs7359397 2.00E-20 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_148415 ATXN2L 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs7359397 2.00E-20 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_003321 TUFM 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs7359397 2.00E-20 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_004551 NDUFS3 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs3817334 2.00E-12 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_153208 IQCK 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs12444979 3.00E-21 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_173808 NEGR1 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs2815752 2.00E-22 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_001035256 POMC 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs713586 6.00E-22 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_003838 TNNI3K 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs1514175 8.00E-14 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_000859 HMGCR 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs2112347 2.00E-13 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_002097 GTF3A 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs4771122 9.00E-10 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_000990 RPL27A 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs4929949 3.00E-09 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_003320 TUB 20935630 http://www.ncbi.nlm.nih.gov/pubmed/20935630 Body mass index rs4929949 3.00E-09 "Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index." NHGRI|-1
NM_177414 PPAP2B 20932310 http://www.ncbi.nlm.nih.gov/pubmed/20932310 AB1-42 rs11206801 6.00E-08 Genome-wide association reveals genetic effects on human Aβ42 and Ï? protein levels in cerebrospinal fluids: a case control study. NHGRI|-1
NM_001128916 TOMM40 20932310 http://www.ncbi.nlm.nih.gov/pubmed/20932310 AB1-42 rs2075650 3.00E-07 Genome-wide association reveals genetic effects on human Aβ42 and Ï? protein levels in cerebrospinal fluids: a case control study. NHGRI|-1
NM_003728 UNC5C 20932310 http://www.ncbi.nlm.nih.gov/pubmed/20932310 P-tau181p rs12643654 5.00E-07 Genome-wide association reveals genetic effects on human Aβ42 and Ï? protein levels in cerebrospinal fluids: a case control study. NHGRI|-1
NM_020864 KIAA1486 20932310 http://www.ncbi.nlm.nih.gov/pubmed/20932310 P-tau181p rs7558386 1.00E-07 Genome-wide association reveals genetic effects on human Aβ42 and Ï? protein levels in cerebrospinal fluids: a case control study. NHGRI|-1
NM_005544 IRS1 20932310 http://www.ncbi.nlm.nih.gov/pubmed/20932310 P-tau181p rs7558386 1.00E-07 Genome-wide association reveals genetic effects on human Aβ42 and Ï? protein levels in cerebrospinal fluids: a case control study. NHGRI|-1
NM_001135098 UPP2 20932310 http://www.ncbi.nlm.nih.gov/pubmed/20932310 P-tau181p rs2074955 1.00E-07 Genome-wide association reveals genetic effects on human Aβ42 and Ï? protein levels in cerebrospinal fluids: a case control study. NHGRI|-1
NM_001201465 NETO1 20932310 http://www.ncbi.nlm.nih.gov/pubmed/20932310 P-tau181p rs1943816 1.00E-07 Genome-wide association reveals genetic effects on human Aβ42 and Ï? protein levels in cerebrospinal fluids: a case control study. NHGRI|-1
NM_152676 FBXO15 20932310 http://www.ncbi.nlm.nih.gov/pubmed/20932310 P-tau181p rs1943816 1.00E-07 Genome-wide association reveals genetic effects on human Aβ42 and Ï? protein levels in cerebrospinal fluids: a case control study. NHGRI|-1
NM_001098535 RFPL3 20932310 http://www.ncbi.nlm.nih.gov/pubmed/20932310 T-tau rs5998432 9.00E-07 Genome-wide association reveals genetic effects on human Aβ42 and Ï? protein levels in cerebrospinal fluids: a case control study. NHGRI|-1
NM_014673 TTC35 20932310 http://www.ncbi.nlm.nih.gov/pubmed/20932310 T-tau rs2935776 6.00E-07 Genome-wide association reveals genetic effects on human Aβ42 and Ï? protein levels in cerebrospinal fluids: a case control study. NHGRI|-1
NM_153015 TMEM74 20932310 http://www.ncbi.nlm.nih.gov/pubmed/20932310 T-tau rs2935776 6.00E-07 Genome-wide association reveals genetic effects on human Aβ42 and Ï? protein levels in cerebrospinal fluids: a case control study. NHGRI|-1
NM_182528 C1QL2 20932310 http://www.ncbi.nlm.nih.gov/pubmed/20932310 T-tau rs17189298 3.00E-07 Genome-wide association reveals genetic effects on human Aβ42 and Ï? protein levels in cerebrospinal fluids: a case control study. NHGRI|-1
NM_194286 SRRM4 20932310 http://www.ncbi.nlm.nih.gov/pubmed/20932310 T-tau rs1997111 1.00E-08 Genome-wide association reveals genetic effects on human Aβ42 and Ï? protein levels in cerebrospinal fluids: a case control study. NHGRI|-1
NM_002042 GABRR1 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Bipolar disorder and schizophrenia rs12201676 4.00E-08 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001184734 ASTN2 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Bipolar disorder and schizophrenia rs11789399 6.00E-09 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_001164436 TMEM212 20889312 http://www.ncbi.nlm.nih.gov/pubmed/20889312 Bipolar disorder and schizophrenia rs6444931 6.00E-07 A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. NHGRI|-1
NM_004827 ABCG2 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Serum urate rs2199936 1.00E-75 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_004827 ABCG2 20884846 http://www.ncbi.nlm.nih.gov/pubmed/20884846 Serum urate rs2199936 3.00E-23 Multiple genetic loci influence serum urate levels and their relationship with gout and cardiovascular disease risk factors. NHGRI|-1
NM_030957 ADAMTS10 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Height rs4072910 4.00E-13 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_022648 TNS1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Height rs1351164 2.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_006548 IGF2BP2 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Height rs720390 2.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NR_027317 C3ORF65 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Height rs720390 2.00E-14 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_006717 SPIN1 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Height rs2778031 9.00E-13 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_001201 BMP3 20881960 http://www.ncbi.nlm.nih.gov/pubmed/20881960 Height rs788867 9.00E-28 Hundreds of variants clustered in genomic loci and biological pathways affect human height. NHGRI|-1
NM_003904 ZNF259 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 LDL cholesterol rs1558861 2.00E-06 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_153706 C5ORF35 20864672 http://www.ncbi.nlm.nih.gov/pubmed/20864672 Triglycerides rs6867983 3.00E-06 Genetic variants influencing circulating lipid levels and risk of coronary artery disease. NHGRI|-1
NM_022158 FN3K 20858683 http://www.ncbi.nlm.nih.gov/pubmed/20858683 Glycated hemoglobin levels rs1046896 2.00E-26 Common variants at 10 genomic loci influence hemoglobin Aâ??(C) levels via glycemic and nonglycemic pathways. NHGRI|-1
NM_178156 FUT8 20802204 http://www.ncbi.nlm.nih.gov/pubmed/20802204 Multiple sclerosis--Brain Glutamate Levels rs8007846 9.00E-06 Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. NHGRI|-1
NR_026731 C14ORF23 20802204 http://www.ncbi.nlm.nih.gov/pubmed/20802204 Multiple sclerosis--Brain Glutamate Levels rs2038256 2.00E-06 Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. NHGRI|-1
NM_000454 SOD1 20801718 http://www.ncbi.nlm.nih.gov/pubmed/20801718 Amyotrophic lateral sclerosis rs13048019 3.00E-08 Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. NHGRI|-1
NM_001195790 SLFN12L 20800221 http://www.ncbi.nlm.nih.gov/pubmed/20800221 Depression--quantitative trait rs8070473 2.00E-06 Genome-wide association scan of trait depression. NHGRI|-1
NM_016841 MAPT 20711177 http://www.ncbi.nlm.nih.gov/pubmed/20711177 Parkinson's disease rs199533 1.00E-06 Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. NHGRI|-1
NM_023067 FOXL2 20711176 http://www.ncbi.nlm.nih.gov/pubmed/20711176 Keloid rs1511412 2.00E-13 A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population. NHGRI|-1
NM_004932 CDH6 20709820 http://www.ncbi.nlm.nih.gov/pubmed/20709820 Emphysema-related traits rs9292394 2.00E-06 Genome-wide Association Study Identifies BICD1 as a Susceptibility Gene for Emphysema. NHGRI|-1
NM_021070 LTBP3 20708005 http://www.ncbi.nlm.nih.gov/pubmed/20708005 Non-alcoholic fatty liver disease histology (lobular) rs6591182 9.00E-07 Genome-wide association study identifies variants associated with histologic features of nonalcoholic Fatty liver disease. NHGRI|-1
NM_001012334 MDK 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11038871 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_017749 AMBRA1 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11038871 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_173811 HARBI1 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11038871 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NR_024588 ATG13 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11038871 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_000506 F2 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11038871 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_001008938 CKAP5 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11038871 2.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_002124 HLA-DRB1 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs2187668 2.00E-33 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_173464 L3MBTL4 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs11662763 5.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_020124 IFNK 20694011 http://www.ncbi.nlm.nih.gov/pubmed/20694011 Immunoglobulin A rs7029145 9.00E-06 Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency. NHGRI|-1
NM_001682 ATP2B1 20700443 http://www.ncbi.nlm.nih.gov/pubmed/20700443 Serum magnesium levels rs7965584 1.00E-16 "Genome-wide association studies of serum magnesium, potassium, and sodium concentrations identify six Loci influencing serum magnesium levels." NHGRI|-1
NM_002959 SORT1 20686565 http://www.ncbi.nlm.nih.gov/pubmed/20686565 Blood lipid traits rs629301 1.00E-170 "Biological, clinical and population relevance of 95 loci for blood lipids." NHGRI|-1
NM_201269 ZNF644 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Metabolic syndrome rs164898 6.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_021127 PMAIP1 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Metabolic syndrome rs12957347 7.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_016433 GLTP 20694148 http://www.ncbi.nlm.nih.gov/pubmed/20694148 Metabolic syndrome rs1085093 3.00E-06 A genome-wide association study of the metabolic syndrome in Indian Asian men. NHGRI|-1
NM_000384 APOB 20707712 http://www.ncbi.nlm.nih.gov/pubmed/20707712 Self-rated health rs17043947 2.00E-07 A genome-wide association study of self-rated health. NHGRI|-1
NM_052920 KLHL29 20707712 http://www.ncbi.nlm.nih.gov/pubmed/20707712 Self-rated health rs17043947 2.00E-07 A genome-wide association study of self-rated health. NHGRI|-1
NM_016179 TRPC4 20707712 http://www.ncbi.nlm.nih.gov/pubmed/20707712 Self-rated health rs9548119 9.00E-06 A genome-wide association study of self-rated health. NHGRI|-1
NM_001145851 PROM1 20707712 http://www.ncbi.nlm.nih.gov/pubmed/20707712 Self-rated health rs17478107 9.00E-06 A genome-wide association study of self-rated health. NHGRI|-1
NM_006826 YWHAQ 20707712 http://www.ncbi.nlm.nih.gov/pubmed/20707712 Self-rated health rs2357266 4.00E-06 A genome-wide association study of self-rated health. NHGRI|-1
NM_005680 TAF1B 20707712 http://www.ncbi.nlm.nih.gov/pubmed/20707712 Self-rated health rs2357266 4.00E-06 A genome-wide association study of self-rated health. NHGRI|-1
NM_001001665 CYP27C1 20707712 http://www.ncbi.nlm.nih.gov/pubmed/20707712 Self-rated health rs7567389 2.00E-06 A genome-wide association study of self-rated health. NHGRI|-1
NM_000122 ERCC3 20707712 http://www.ncbi.nlm.nih.gov/pubmed/20707712 Self-rated health rs7567389 2.00E-06 A genome-wide association study of self-rated health. NHGRI|-1
NM_031914 SYT16 20707712 http://www.ncbi.nlm.nih.gov/pubmed/20707712 Self-rated health rs6573416 3.00E-06 A genome-wide association study of self-rated health. NHGRI|-1
NR_036437 KCNC4 20707712 http://www.ncbi.nlm.nih.gov/pubmed/20707712 Self-rated health rs958798 4.00E-07 A genome-wide association study of self-rated health. NHGRI|-1
NM_014903 NAV3 20707712 http://www.ncbi.nlm.nih.gov/pubmed/20707712 Self-rated health rs300489 5.00E-06 A genome-wide association study of self-rated health. NHGRI|-1
NM_000312 PROC 20707712 http://www.ncbi.nlm.nih.gov/pubmed/20707712 Self-rated health rs1799810 9.00E-06 A genome-wide association study of self-rated health. NHGRI|-1
NM_001005502 CPM 20673876 http://www.ncbi.nlm.nih.gov/pubmed/20673876 Major depressive disorder rs9943849 3.00E-06 "Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression." NHGRI|-1
NM_004272 HOMER1 20673876 http://www.ncbi.nlm.nih.gov/pubmed/20673876 Major depressive disorder rs7713917 1.00E-06 "Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression." NHGRI|-1
NM_002473 MYH9 20668430 http://www.ncbi.nlm.nih.gov/pubmed/20668430 Glomerulosclerosis rs2239785 5.00E-13 A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9. NHGRI|-1
NM_152588 TMTC2 20662065 http://www.ncbi.nlm.nih.gov/pubmed/20662065 Neonatal lupus rs2403106 3.00E-06 Identification of candidate loci at 6p21 and 21q22 in a genome-wide association study of cardiac manifestations of neonatal lupus. NHGRI|-1
NM_001166598 APOA5 20657596 http://www.ncbi.nlm.nih.gov/pubmed/20657596 Hypertriglyceridemia rs964184 5.00E-24 Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia. NHGRI|-1
NM_002124 HLA-DRB1 20639878 http://www.ncbi.nlm.nih.gov/pubmed/20639878 Lumiracoxib-related liver injury rs3129900 7.00E-25 A genome-wide study identifies HLA alleles associated with lumiracoxib-related liver injury. NHGRI|-1
NM_000165 GJA1 20639392 http://www.ncbi.nlm.nih.gov/pubmed/20639392 Resting heart rate rs9398652 4.00E-15 Genome-wide association analysis identifies multiple loci related to resting heart rate. NHGRI|-1
NM_000545 HNF1A 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 Type 2 diabetes rs7957197 2.00E-08 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_003483 HMGA2 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 Type 2 diabetes rs1531343 4.00E-09 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_138712 PPARG 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 Type 2 diabetes rs13081389 2.00E-07 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_032367 ZBED3 20581827 http://www.ncbi.nlm.nih.gov/pubmed/20581827 Type 2 diabetes rs4457053 3.00E-12 Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. NHGRI|-1
NM_007113 TCHH 20585627 http://www.ncbi.nlm.nih.gov/pubmed/20585627 Common traits (Other) rs17646946 2.00E-42 "Web-based, participant-driven studies yield novel genetic associations for common traits." NHGRI|-1
NM_020374 C12ORF4 20558539 http://www.ncbi.nlm.nih.gov/pubmed/20558539 Serum phosphorus levels rs2970818 4.00E+09 Common genetic variants associate with serum phosphorus concentration. NHGRI|-1
NM_002968 SALL1 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Optic disc parameters rs1362756 5.00E-09 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_020680 SCYL1 20548946 http://www.ncbi.nlm.nih.gov/pubmed/20548946 Vertical cup-disc ratio rs17146964 4.00E-09 A genome-wide association study of optic disc parameters. NHGRI|-1
NM_002473 MYH9 20532800 http://www.ncbi.nlm.nih.gov/pubmed/20532800 End-stage renal disease (non-diabetic) rs4821469 2.00E-19 Candidate genes for non-diabetic ESRD in African Americans: a genome-wide association study using pooled DNA. NHGRI|-1
NM_006510 TRIM27 20526338 http://www.ncbi.nlm.nih.gov/pubmed/20526338 Platelet aggregation rs4947339 2.00E-06 Genome-wide meta-analyses identifies seven loci associated with platelet aggregation in response to agonists. NHGRI|-1
NM_007045 FGFR1OP 20526339 http://www.ncbi.nlm.nih.gov/pubmed/20526339 Vitiligo rs2236313 1.00E-16 Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. NHGRI|-1
NM_031409 CCR6 20526339 http://www.ncbi.nlm.nih.gov/pubmed/20526339 Vitiligo rs2236313 1.00E-16 Genome-wide association study for vitiligo identifies susceptibility loci at 6q27 and the MHC. NHGRI|-1
NM_002116 HLA-A 20512145 http://www.ncbi.nlm.nih.gov/pubmed/20512145 Nasopharyngeal carcinoma rs2860580 5.00E-67 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci. NHGRI|-1
NR_026554 CALCOCO1 20460270 http://www.ncbi.nlm.nih.gov/pubmed/20460270 Biliary atresia rs2120991 9.00E-06 Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. NHGRI|-1
NM_002124 HLA-DRB1 20453841 http://www.ncbi.nlm.nih.gov/pubmed/20453841 Rheumatoid arthritis rs13192471 2.00E-58 A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility. NHGRI|-1
NM_012481 IKZF3 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 Rheumatoid arthritis rs2872507 9.00E-07 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_003820 TNFRSF14 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 Rheumatoid arthritis rs3890745 4.00E-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_002989 CCL21 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 Rheumatoid arthritis rs951005 4.00E-10 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NR_024481 C9ORF144 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 Rheumatoid arthritis rs951005 4.00E-10 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_017771 PXK 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 Rheumatoid arthritis rs13315591 5.00E-08 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_002124 HLA-DRB1 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 Rheumatoid arthritis rs6910071 1.00E-299 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_006257 PRKCQ 20453842 http://www.ncbi.nlm.nih.gov/pubmed/20453842 Rheumatoid arthritis rs4750316 2.00E-06 Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. NHGRI|-1
NM_002339 LSP1 20453838 http://www.ncbi.nlm.nih.gov/pubmed/20453838 Breast cancer rs909116 7.00E-07 Genome-wide association study identifies five new breast cancer susceptibility loci. NHGRI|-1
NM_001193451 TMTC1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart failure rs2046383 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_024761 MOBKL2B 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart failure rs10812610 5.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_152837 SNX16 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart failure rs6473383 3.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_001144881 PRICKLE1 20445134 http://www.ncbi.nlm.nih.gov/pubmed/20445134 Heart failure rs1520832 1.00E-06 Association of genome-wide variation with the risk of incident heart failure in adults of European and African ancestry: a prospective meta-analysis from the cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium. NHGRI|-1
NM_000888 ITGB6 20418489 http://www.ncbi.nlm.nih.gov/pubmed/20418489 Type 2 diabetes rs7593730 4.00E-08 Genetic variants at 2q24 are associated with susceptibility to type 2 diabetes. NHGRI|-1
NM_022054 KCNK13 20400778 http://www.ncbi.nlm.nih.gov/pubmed/20400778 Mortality among heart failure patients rs8017423 7.00E-06 Genomic variation associated with mortality among adults of European and African ancestry with heart failure: the cohorts for heart and aging research in genomic epidemiology consortium. NHGRI|-1
NM_000362 TIMP3 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Age-related macular degeneration rs9621532 1.00E-11 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_000204 CFI 20385819 http://www.ncbi.nlm.nih.gov/pubmed/20385819 Age-related macular degeneration rs2285714 3.00E-07 Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration. NHGRI|-1
NM_000362 TIMP3 20385826 http://www.ncbi.nlm.nih.gov/pubmed/20385826 Age-related macular degeneration rs9621532 4.00E-09 Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC). NHGRI|-1
NM_001126335 SLC7A9 20383145 http://www.ncbi.nlm.nih.gov/pubmed/20383145 Serum creatinine rs4805834 5.00E-11 Genetic loci influencing kidney function and chronic kidney disease. NHGRI|-1
NM_006286 TFDP2 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Chronic kidney disease rs347685 3.00E-11 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001122633 CPS1 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Chronic kidney disease rs7422339 1.00E-15 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_015662 IFT172 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Chronic kidney disease rs1260326 3.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_022823 FNDC4 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Chronic kidney disease rs1260326 3.00E-14 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001042784 CCDC158 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Chronic kidney disease rs17319721 1.00E-19 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_001122847 SLC6A12 20383146 http://www.ncbi.nlm.nih.gov/pubmed/20383146 Chronic kidney disease rs10774021 1.00E-09 New loci associated with kidney function and chronic kidney disease. NHGRI|-1
NM_022454 SOX17 20364137 http://www.ncbi.nlm.nih.gov/pubmed/20364137 Intracranial aneurysm rs9298506 1.00E-12 Genome-wide association study of intracranial aneurysm identifies three new risk loci. NHGRI|-1
NM_000426 LAMA2 20397748 http://www.ncbi.nlm.nih.gov/pubmed/20397748 Body mass index rs2275215 4.00E-07 Genome-wide association study of height and body mass index in Australian twin families. NHGRI|-1
NM_015254 KIF13B 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs10091038 3.00E-08 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_024945 RMI1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs10123041 6.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001616 ACVR2A 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs7584099 5.00E-07 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001080480 MBOAT1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs16883019 7.00E-07 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_175611 GRIK1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs9305406 8.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_199328 CLDN8 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs9305406 8.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_002959 SORT1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs646776 4.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001164538 DISC1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs10746514 1.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_182828 GDF7 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs541041 8.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_006614 CHL1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs4684585 9.00E-07 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_000128 F11 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs13148903 3.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_000892 KLKB1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs13148903 3.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001178094 BCAT1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs7979575 2.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_004490 GRB14 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs10221833 6.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_177438 DICER1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs8014194 2.00E-08 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_013402 FADS1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs1535 7.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001083112 GPD2 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs16839962 9.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_013402 FADS1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs174583 3.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_021727 FADS3 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs174583 3.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001080497 MEGF9 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs16909449 1.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_173685 NSMCE2 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs2954038 7.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_018368 LMBRD1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs3757057 4.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_001858 COL19A1 20339536 http://www.ncbi.nlm.nih.gov/pubmed/20339536 Response to statin therapy rs3757057 4.00E-06 Genome-wide association of lipid-lowering response to statins in combined study populations. NHGRI|-1
NM_020056 HLA-DQA2 20305777 http://www.ncbi.nlm.nih.gov/pubmed/20305777 Knee osteoarthritis rs10947262 5.00E-09 New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study. NHGRI|-1
NM_002123 HLA-DQB1 20305777 http://www.ncbi.nlm.nih.gov/pubmed/20305777 Knee osteoarthritis rs10947262 5.00E-09 New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study. NHGRI|-1
NM_019111 HLA-DRA 20228798 http://www.ncbi.nlm.nih.gov/pubmed/20228798 Ulcerative colitis rs9268923 4.00E-15 Genome-wide association study for ulcerative colitis identifies risk loci at 7q22 and 22q13 (IL17REL). NHGRI|-1
NM_139281 WDR36 20208534 http://www.ncbi.nlm.nih.gov/pubmed/20208534 Eosinophilic esophagitis (pediatric) rs3806932 3.00E-09 Common variants at 5q22 associate with pediatric eosinophilic esophagitis. NHGRI|-1
NM_003855 IL18R1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs917997 1.00E-15 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_016232 IL1RL1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs917997 1.00E-15 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_003854 IL1RL2 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs917997 1.00E-15 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_005214 CTLA4 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs4675374 6.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_006139 CD28 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs4675374 6.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001123396 CCR2 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs13098911 3.00E-17 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_003965 CCRL2 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs13098911 3.00E-17 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_178329 CCR3 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs13098911 3.00E-17 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001100168 CCR5 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs13098911 3.00E-17 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_031200 CCR9 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs13098911 3.00E-17 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_021803 IL21 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs13151961 2.00E-27 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_002123 HLA-DQB1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs2187668 1.00E-50 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_005475 SH2B3 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs653178 7.00E-21 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_003820 TNFRSF14 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs3748816 3.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001561 TNFRSF9 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs12727642 9.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_003326 TNFSF4 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs859637 2.00E-06 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_002908 REL 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs13003464 4.00E-13 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_152392 AHSA2 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs13003464 4.00E-13 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_005191 CD80 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs11712165 8.00E-09 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_003188 MAP3K7 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs10806425 4.00E-10 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_001164685 THEMIS 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs802734 3.00E-14 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NR_028437 UBE2L3 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs2298428 2.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_016562 TLR7 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs5979785 6.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_000246 CIITA 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs12928822 3.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_003745 SOCS1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs12928822 3.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_015226 CLEC16A 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs12928822 3.00E-08 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_004926 ZFP36L1 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs4899260 4.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_207442 C14ORF181 20190752 http://www.ncbi.nlm.nih.gov/pubmed/20190752 Celiac disease rs4899260 4.00E-07 Multiple common variants for celiac disease influencing immune gene expression. NHGRI|-1
NM_022346 NCAPG 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Height rs7678436 8.00E-15 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_153686 LCORL 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Height rs7678436 8.00E-15 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_178138 LHX3 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Height rs12338076 2.00E-08 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_002181 IHH 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Height rs16859517 5.00E-06 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_145902 HMGA1 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Height rs7742369 1.00E-13 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_006856 ATF7 20189936 http://www.ncbi.nlm.nih.gov/pubmed/20189936 Height rs11170631 9.00E-07 A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci. NHGRI|-1
NM_022475 HHIP 20173748 http://www.ncbi.nlm.nih.gov/pubmed/20173748 Chronic obstructive pulmonary disease rs13118928 5.00E-07 Variants in FAM13A are associated with chronic obstructive pulmonary disease. NHGRI|-1
NM_201252 AKR7L 20171287 http://www.ncbi.nlm.nih.gov/pubmed/20171287 Brain structure rs710865 1.00E-07 Voxelwise genome-wide association study (vGWAS). NHGRI|-1
NM_001122633 CPS1 20154341 http://www.ncbi.nlm.nih.gov/pubmed/20154341 Homocysteine levels rs7422339 5.00E-09 Genome-wide association study of homocysteine levels in Filipinos provides evidence for CPS1 in women and a stronger MTHFR effect in young adults. NHGRI|-1
NM_031938 BCO2 20150558 http://www.ncbi.nlm.nih.gov/pubmed/20150558 Interleukin-18 levels rs1834481 1.00E-08 Genome-wide association study identifies variants at the IL18-BCO2 locus associated with interleukin-18 levels. NHGRI|-1
NM_015094 HIC2 20139978 http://www.ncbi.nlm.nih.gov/pubmed/20139978 Hematological and biochemical traits rs4821112 1.00E-08 Genome-wide association study of hematological and biochemical traits in a Japanese population. NHGRI|-1
NM_001166167 NEK6 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs2807580 3.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_003821 RIPK2 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs4397449 3.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_005941 MMP16 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs4397449 3.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_004980 KCND3 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs7555668 3.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_005421 TAL2 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs1463984 3.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_018112 TMEM38B 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs1463984 3.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_002236 KCNF1 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs6739054 2.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001134437 PHLDB2 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs4450776 5.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_153268 PLCXD2 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs4450776 5.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_138960 TGIF2LX 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs5941436 5.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_004796 NRXN3 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs6574433 6.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_002417 MKI67 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs9804317 7.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_002412 MGMT 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs9804317 7.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001099439 EPHA10 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs12117544 8.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001113482 MANEAL 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs12117544 8.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NR_026814 C8ORF12 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs2002030 5.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_182946 NIN 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs8020441 5.00E-07 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_014989 RIMS1 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs10455248 4.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_004196 CDKL1 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs1265879 4.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001166550 IDS 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs530501 4.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_016358 IRX4 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs17586674 5.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001134222 IRX2 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs17586674 5.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001040630 NCALD 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs517811 5.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_002095 GTF2E2 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs2978263 8.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NR_027049 ZNF788 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs17638629 7.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001257 CDH13 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs3784962 3.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_015912 FAM135B 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs9657451 2.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001098500 KIAA1217 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs2484873 4.00E-07 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_007028 TRIM31 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs34704616 6.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_013381 TRHDE 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs10879517 4.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_004571 PKNOX1 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs234720 2.00E-07 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_015279 TBC1D30 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs939876 2.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_014619 GRIK4 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs12797755 8.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_032550 AFAP1L2 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs4751674 4.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001941 DSC3 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs4145170 3.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_139056 ADAMTS16 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs492478 4.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_033225 CSMD1 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs2616984 4.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001130849 CAB39 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs17275498 8.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_001002919 FAM150B 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs4643574 5.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_152834 TMEM18 20125193 http://www.ncbi.nlm.nih.gov/pubmed/20125193 Cognitive test performance rs4643574 5.00E-06 Common genetic variation and performance on standardized cognitive tests. NHGRI|-1
NM_005272 GNAT2 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 Major depressive disorder rs6537837 1.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_139156 AMPD2 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 Major depressive disorder rs6537837 1.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_001040709 SYPL2 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 Major depressive disorder rs12049330 6.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_001134402 CYB561D1 20125088 http://www.ncbi.nlm.nih.gov/pubmed/20125088 Major depressive disorder rs12049330 6.00E-06 Genome-wide association study of recurrent early-onset major depressive disorder. NHGRI|-1
NM_001730 KLF5 20101243 http://www.ncbi.nlm.nih.gov/pubmed/20101243 Pancreatic cancer rs9543325 3.00E-11 "A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33." NHGRI|-1
NM_001128916 TOMM40 20100581 http://www.ncbi.nlm.nih.gov/pubmed/20100581 Brain imaging rs2075650 NS Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort. NHGRI|-1
NM_003722 TP63 20100581 http://www.ncbi.nlm.nih.gov/pubmed/20100581 Brain imaging rs7610017 NS Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort. NHGRI|-1
NM_004438 EPHA4 20100581 http://www.ncbi.nlm.nih.gov/pubmed/20100581 Brain imaging rs10932886 E Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort. NHGRI|-1
NM_016841 MAPT 20070850 http://www.ncbi.nlm.nih.gov/pubmed/20070850 Parkinson's disease rs11012 6.00E-08 Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. NHGRI|-1
NM_015847 MBD1 20062064 http://www.ncbi.nlm.nih.gov/pubmed/20062064 Chronic lymphocytic leukemia rs1036935 2.00E-06 "Common variants at 2q37.3, 8q24.21, 15q21.3 and 16q24.1 influence chronic lymphocytic leukemia risk." NHGRI|-1
NM_012242 DKK1 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiographic traits rs1733724 7.00E-08 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_001130487 NDRG4 20062063 http://www.ncbi.nlm.nih.gov/pubmed/20062063 Electrocardiographic traits rs37062 1.00E-06 "Several common variants modulate heart rate, PR interval and QRS duration." NHGRI|-1
NM_004387 NKX2-5 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 PR interval rs251253 9.00E-13 Genome-wide association study of PR interval. NHGRI|-1
NM_181486 TBX5 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 PR interval rs1896312 3.00E-17 Genome-wide association study of PR interval. NHGRI|-1
NM_152989 SOX5 20062060 http://www.ncbi.nlm.nih.gov/pubmed/20062060 PR interval rs11047543 3.00E-13 Genome-wide association study of PR interval. NHGRI|-1
NM_003720 PSMG1 20062062 http://www.ncbi.nlm.nih.gov/pubmed/20062062 Ankylosing spondylitis rs2242944 8.00E-20 Genome-wide association study of ankylosing spondylitis identifies non-MHC susceptibility loci. NHGRI|-1
NM_172140 IL29 20060832 http://www.ncbi.nlm.nih.gov/pubmed/20060832 Chronic Hepatitis C infection rs8099917 6.00E-09 Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study. NHGRI|-1
NM_001166019 AP1B1 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Carotid atherosclerosis in HIV infection rs13053817 2.00E-06 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_001002879 THOC5 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Carotid atherosclerosis in HIV infection rs13053817 2.00E-06 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_000268 NF2 20009918 http://www.ncbi.nlm.nih.gov/pubmed/20009918 Carotid atherosclerosis in HIV infection rs13053817 2.00E-06 A genome-wide association study of carotid atherosclerosis in HIV-infected men. NHGRI|-1
NM_005514 HLA-B 20045101 http://www.ncbi.nlm.nih.gov/pubmed/20045101 CD4:CD8 lymphocyte ratio rs2524054 6.00E-21 Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. NHGRI|-1
NM_005514 HLA-B 20045101 http://www.ncbi.nlm.nih.gov/pubmed/20045101 CD4:CD8 lymphocyte ratio rs2524054 2.00E-28 Quantitative trait loci for CD4:CD8 lymphocyte ratio are associated with risk of type 1 diabetes and HIV-1 immune control. NHGRI|-1
NM_001142324 SLC18A1 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 Major depressive disorder (broad) rs1106634 7.00E-07 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_021020 LZTS1 20038947 http://www.ncbi.nlm.nih.gov/pubmed/20038947 Major depressive disorder (broad) rs1106634 7.00E-07 Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies. NHGRI|-1
NM_004453 ETFDH 20037589 http://www.ncbi.nlm.nih.gov/pubmed/20037589 Serum metabolites rs8396 4.00E-24 A genome-wide perspective of genetic variation in human metabolism. NHGRI|-1
NM_004557 NOTCH4 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 control rs3763313 2.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_170783 ZNRD1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 control rs259919 3.00E-07 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_005514 HLA-B 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 control rs2395029 5.00E-35 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_002117 HLA-C 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 control rs9264942 6.00E-12 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001264 CDSN 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 control rs3815087 8.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_002117 HLA-C 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 control rs9264942 6.00E-32 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_005514 HLA-B 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 control rs2395029 1.00E-11 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_170783 ZNRD1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 control rs7758512 2.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_025236 RNF39 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 control rs7758512 2.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_002116 HLA-A 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 control rs7758512 2.00E-08 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_020442 VARS2 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 control rs7756521 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_080870 DPCR1 20041166 http://www.ncbi.nlm.nih.gov/pubmed/20041166 HIV-1 control rs7756521 1.00E-06 Common genetic variation and the control of HIV-1 in humans. NHGRI|-1
NM_001195215 DENND1B 20032318 http://www.ncbi.nlm.nih.gov/pubmed/20032318 Asthma rs2786098 2.00E-13 Variants of DENND1B associated with asthma in children. NHGRI|-1
NM_005450 NOG 20023658 http://www.ncbi.nlm.nih.gov/pubmed/20023658 Nonsyndromic cleft lip with or without cleft palate rs17760296 7.00E-06 Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate. NHGRI|-1
NM_022475 HHIP 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Pulmonary function rs1980057 3.00E-20 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_001184690 NPNT 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Pulmonary function rs11727189 5.00E-17 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_024751 GSTCD 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Pulmonary function rs11727189 5.00E-17 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_138717 PPT2 20010835 http://www.ncbi.nlm.nih.gov/pubmed/20010835 Pulmonary function rs2070600 3.00E-14 Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function. NHGRI|-1
NM_022475 HHIP 20010834 http://www.ncbi.nlm.nih.gov/pubmed/20010834 Pulmonary function rs12504628 6.00E-13 Genome-wide association study identifies five loci associated with lung function. NHGRI|-1
NM_003836 DLK1 19966805 http://www.ncbi.nlm.nih.gov/pubmed/19966805 Type 1 diabetes rs941576 1.00E-10 The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes. NHGRI|-1
NM_001362 DIO3 19966805 http://www.ncbi.nlm.nih.gov/pubmed/19966805 Type 1 diabetes rs941576 1.00E-10 The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes. NHGRI|-1
NM_005330 HBE1 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Beta thalassemia/hemoglobin E disease rs2071348 3.00E-15 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_000184 HBG2 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Beta thalassemia/hemoglobin E disease rs2071348 3.00E-15 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_000559 HBG1 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Beta thalassemia/hemoglobin E disease rs2071348 3.00E-15 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_000519 HBD 20183929 http://www.ncbi.nlm.nih.gov/pubmed/20183929 Beta thalassemia/hemoglobin E disease rs2071348 3.00E-15 A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E. NHGRI|-1
NM_004972 JAK2 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 Ulcerative colitis rs10975003 1.00E-06 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_182488 USP12 19915573 http://www.ncbi.nlm.nih.gov/pubmed/19915573 Ulcerative colitis rs17085007 7.00E-08 A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population. NHGRI|-1
NM_020998 MST1 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 Ulcerative colitis rs9858542 7.00E-09 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_017596 KIF21B 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 Ulcerative colitis rs7554511 1.00E-06 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_004360 CDH1 19915572 http://www.ncbi.nlm.nih.gov/pubmed/19915572 Ulcerative colitis rs1728785 3.00E-08 "Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region." NHGRI|-1
NM_021090 MTMR3 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory bowel disease (early onset) rs2412973 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_002309 LIF 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory bowel disease (early onset) rs2412973 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_145659 IL27 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory bowel disease (early onset) rs8049439 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_138414 CCDC101 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory bowel disease (early onset) rs8049439 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_001042432 CLN3 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory bowel disease (early onset) rs8049439 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_012385 NUPR1 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory bowel disease (early onset) rs8049439 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_177536 SULT1A1 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory bowel disease (early onset) rs8049439 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_177528 SULT1A2 19915574 http://www.ncbi.nlm.nih.gov/pubmed/19915574 Inflammatory bowel disease (early onset) rs8049439 2.00E-09 Common variants at five new loci associated with early-onset inflammatory bowel disease. NHGRI|-1
NM_033102 SLC45A3 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson's disease rs947211 2.00E-12 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_022731 NUCKS1 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson's disease rs947211 2.00E-12 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_198578 LRRK2 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson's disease rs1994090 3.00E-08 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_004334 BST1 19915576 http://www.ncbi.nlm.nih.gov/pubmed/19915576 Parkinson's disease rs4538475 3.00E-09 Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease. NHGRI|-1
NM_003943 STBD1 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson's disease rs6812193 4.00E-07 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_016841 MAPT 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson's disease rs393152 2.00E-16 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_001193465 KIAA1267 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson's disease rs393152 2.00E-16 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_001136200 C10ORF32 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson's disease rs17115100 7.00E-08 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_199077 CNNM2 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson's disease rs17115100 7.00E-08 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_178858 SFXN2 19915575 http://www.ncbi.nlm.nih.gov/pubmed/19915575 Parkinson's disease rs17115100 7.00E-08 Genome-wide association study reveals genetic risk underlying Parkinson's disease. NHGRI|-1
NM_001037172 ACPL2 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Height rs10513137 8.00E-08 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_005994 TBX2 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Height rs2079795 3.00E-06 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_145902 HMGA1 19893584 http://www.ncbi.nlm.nih.gov/pubmed/19893584 Height rs6918981 2.00E-08 Identification of 15 loci influencing height in a Korean population. NHGRI|-1
NM_005603 ATP8B1 19890347 http://www.ncbi.nlm.nih.gov/pubmed/19890347 Vitiligo rs10503019 3.00E-06 "Genome-wide association study of generalized vitiligo in an isolated European founder population identifies SMOC2, in close proximity to IDDM8." NHGRI|-1
NM_139011 HFE 19853236 http://www.ncbi.nlm.nih.gov/pubmed/19853236 Hematology traits rs1408272 1.00E-11 Sequence variants in three loci influence monocyte counts and erythrocyte volume. NHGRI|-1
NM_015094 HIC2 19838193 http://www.ncbi.nlm.nih.gov/pubmed/19838193 Systemic lupus erythematosus rs131654 1.00E-16 Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus. NHGRI|-1
NM_019101 APOM 19836008 http://www.ncbi.nlm.nih.gov/pubmed/19836008 Lung adenocarcinoma rs3117582 5.00E-12 A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma. NHGRI|-1
NM_139011 HFE 19820698 http://www.ncbi.nlm.nih.gov/pubmed/19820698 Hemoglobin rs198846 1.00E-08 Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels. NHGRI|-1
NM_005475 SH2B3 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hematocrit rs11065987 1.00E-12 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001143906 TRAFD1 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Hemoglobin rs11065987 1.00E-11 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_004053 BYSL 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Mean corpuscular hemoglobin rs9349205 8.00E-20 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_004053 BYSL 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Mean corpuscular volume rs9349205 1.00E-31 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_001142403 CD164 19862010 http://www.ncbi.nlm.nih.gov/pubmed/19862010 Mean corpuscular volume rs9374080 4.00E-10 Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium. NHGRI|-1
NM_004053 BYSL 19820697 http://www.ncbi.nlm.nih.gov/pubmed/19820697 Hematological parameters rs11970772 7.00E-19 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. NHGRI|-1
NM_003966 SEMA5A 19812673 http://www.ncbi.nlm.nih.gov/pubmed/19812673 Autism rs10513025 3.00E-07 A genome-wide linkage and association scan reveals novel loci for autism. NHGRI|-1
NM_001098210 CTNNB1 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone mineral density (hip) rs87938 8.00E-10 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_016248 AKAP11 19801982 http://www.ncbi.nlm.nih.gov/pubmed/19801982 Bone mineral density (spine) rs9533090 5.00E-25 Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies. NHGRI|-1
NM_030791 SGPP1 19798445 http://www.ncbi.nlm.nih.gov/pubmed/19798445 Sphingolipid levels rs7157785 9.00E-66 Genetic determinants of circulating sphingolipid concentrations in European populations. NHGRI|-1
NM_001334 CTSO 19786962 http://www.ncbi.nlm.nih.gov/pubmed/19786962 Speech perception in dyslexia rs4234898 5.00E-08 First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children. NHGRI|-1
NM_001142615 EHBP1 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostate cancer rs6545977 5.00E-07 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001127598 IGF2 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostate cancer rs7127900 3.00E-33 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NR_028043 IGF2AS 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostate cancer rs7127900 3.00E-33 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001185098 INS 19767753 http://www.ncbi.nlm.nih.gov/pubmed/19767753 Prostate cancer rs7127900 3.00E-33 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study. NHGRI|-1
NM_001831 CLU 19734903 http://www.ncbi.nlm.nih.gov/pubmed/19734903 Alzheimer's disease rs2279590 6.00E-10 Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. NHGRI|-1
NM_001831 CLU 19734903 http://www.ncbi.nlm.nih.gov/pubmed/19734903 Alzheimer's disease rs11136000 6.00E-10 Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. NHGRI|-1
NM_001831 CLU 19734903 http://www.ncbi.nlm.nih.gov/pubmed/19734903 Alzheimer's disease rs9331888 6.00E-10 Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease. NHGRI|-1
NM_181876 PPP2R2C 19734900 http://www.ncbi.nlm.nih.gov/pubmed/19734900 Type 2 diabetes and other traits rs4689388 1.00E-08 "Genetic variant near IRS1 is associated with type 2 diabetes, insulin resistance and hyperinsulinemia." NHGRI|-1
NM_024761 MOBKL2B 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic lateral sclerosis rs3849942 1.00E-08 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_024761 MOBKL2B 19734901 http://www.ncbi.nlm.nih.gov/pubmed/19734901 Amyotrophic lateral sclerosis rs2814707 7.00E-09 Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. NHGRI|-1
NR_023928 C18ORF2 19727025 http://www.ncbi.nlm.nih.gov/pubmed/19727025 Exercise (leisure time) rs8097348 7.00E-06 Genome-Wide Association Study of Exercise Behavior in Dutch and American Adults. NHGRI|-1
NM_000771 CYP2C9 19706858 http://www.ncbi.nlm.nih.gov/pubmed/19706858 Response to clopidogrel therapy rs12777823 2.00E-13 Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy. NHGRI|-1
NM_001198853 CYP2C8 19706858 http://www.ncbi.nlm.nih.gov/pubmed/19706858 Response to clopidogrel therapy rs12777823 2.00E-13 Association of cytochrome P450 2C19 genotype with the antiplatelet effect and clinical efficacy of clopidogrel therapy. NHGRI|-1
NM_006768 BRAP 19698717 http://www.ncbi.nlm.nih.gov/pubmed/19698717 Esophageal cancer rs671 3.00E-24 Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk. NHGRI|-1
NM_001102470 ADH6 19698717 http://www.ncbi.nlm.nih.gov/pubmed/19698717 Esophageal cancer rs1229984 8.00E-24 Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk. NHGRI|-1
NR_023928 C18ORF2 19684603 http://www.ncbi.nlm.nih.gov/pubmed/19684603 Acute lymphoblastic leukemia (childhood) rs1879352 9.00E-06 Germline genomic variants associated with childhood acute lymphoblastic leukemia. NHGRI|-1
NM_005779 LHFPL2 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampal atrophy rs6881634 2.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_152641 ARID2 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampal atrophy rs1373549 8.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_018448 CAND1 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampal atrophy rs1082714 5.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_152330 FRMD6 19668339 http://www.ncbi.nlm.nih.gov/pubmed/19668339 Hippocampal atrophy rs11626056 1.00E-06 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease. NHGRI|-1
NM_021903 GABBR1 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal carcinoma rs29232 9.00E-17 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_018950 HLA-F 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal carcinoma rs3129055 7.00E-11 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_002116 HLA-A 19664746 http://www.ncbi.nlm.nih.gov/pubmed/19664746 Nasopharyngeal carcinoma rs2517713 4.00E-20 Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21.3. NHGRI|-1
NM_017738 CNTLN 19648919 http://www.ncbi.nlm.nih.gov/pubmed/19648919 Ovarian cancer rs3814113 5.00E-19 A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2. NHGRI|-1
NM_001191016 CASP12 20031604 http://www.ncbi.nlm.nih.gov/pubmed/20031604 Serum matrix metalloproteinase rs11226373 2.00E-18 Genome-wide association scan identifies variants near Matrix Metalloproteinase (MMP) genes on chromosome 11q21-22 strongly associated with serum MMP-1 levels. NHGRI|-1
NM_001029858 SLC35F1 19587794 http://www.ncbi.nlm.nih.gov/pubmed/19587794 QT interval rs11153730 2.00E-29 Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies. NHGRI|-1
NM_002667 PLN 19587794 http://www.ncbi.nlm.nih.gov/pubmed/19587794 QT interval rs11153730 2.00E-29 Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies. NHGRI|-1
NM_021947 SRR 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aortic root size rs10852932 2.00E-11 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_018128 TSR1 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aortic root size rs10852932 2.00E-11 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_014853 SGSM2 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aortic root size rs10852932 2.00E-11 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_000943 PPIC 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Aortic root size rs17470137 1.00E-11 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_001042475 C6ORF204 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Cardiac structure and function rs89107 1.00E-09 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_002667 PLN 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Cardiac structure and function rs89107 1.00E-09 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_138773 SLC25A46 19584346 http://www.ncbi.nlm.nih.gov/pubmed/19584346 Cardiac structure and function rs17132261 9.00E-07 Genetic variants associated with cardiac structure and function: a meta-analysis and replication of genome-wide association data. NHGRI|-1
NM_000077 CDKN2A 19578364 http://www.ncbi.nlm.nih.gov/pubmed/19578364 Melanoma rs7023329 4.00E-07 Genome-wide association study identifies three loci associated with melanoma risk. NHGRI|-1
NM_000077 CDKN2A 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs4977756 7.00E-15 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_004936 CDKN2B 19578367 http://www.ncbi.nlm.nih.gov/pubmed/19578367 Glioma rs4977756 7.00E-15 Genome-wide association study identifies five susceptibility loci for glioma. NHGRI|-1
NM_175607 CNTN4 19578179 http://www.ncbi.nlm.nih.gov/pubmed/19578179 Acenocoumarol maintenance dosage rs10935268 8.00E-07 A genome-wide association study of acenocoumarol maintenance dosage. NHGRI|-1
NM_000908 NPR3 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Height rs10472828 3.00E-07 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_001193537 TMEM126B 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Height rs10898392 3.00E-06 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_000026 ADSL 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Height rs139909 2.00E-07 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_001632 ALPP 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Height rs6717918 3.00E-09 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_024409 NPPC 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Height rs6717918 3.00E-09 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_015705 SGSM3 19570815 http://www.ncbi.nlm.nih.gov/pubmed/19570815 Height rs5757949 4.00E-06 A genome-wide association study of northwestern Europeans involves the C-type natriuretic peptide signaling pathway in the etiology of human height variation. NHGRI|-1
NM_005087 FXR1 19571811 http://www.ncbi.nlm.nih.gov/pubmed/19571811 Schizophrenia rs6782299 1.00E-07 Common polygenic variation contributes to risk of schizophrenia and bipolar disorder. NHGRI|-1
NM_005074 SLC17A1 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs13194053 1.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_001098486 SLC17A3 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs13194053 1.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_001197247 BTN3A2 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs13194053 1.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_001197238 BTN2A2 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs13194053 1.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_194441 BTN3A1 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs13194053 1.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_005865 PRSS16 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs13194053 1.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_007149 ZNF184 19571809 http://www.ncbi.nlm.nih.gov/pubmed/19571809 Schizophrenia rs13194053 1.00E-08 Common variants on chromosome 6p22.1 are associated with schizophrenia. NHGRI|-1
NM_001042440 CAST 19581569 http://www.ncbi.nlm.nih.gov/pubmed/19581569 Alcohol dependence rs13160562 7.00E-06 Genome-wide association study of alcohol dependence. NHGRI|-1
NM_138694 PKHD1 19557197 http://www.ncbi.nlm.nih.gov/pubmed/19557197 Waist circumference rs1555967 3.00E-06 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. NHGRI|-1
NM_012306 FAIM2 19557197 http://www.ncbi.nlm.nih.gov/pubmed/19557197 Waist circumference rs7138803 8.00E-07 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. NHGRI|-1
NM_012331 MSRA 19557161 http://www.ncbi.nlm.nih.gov/pubmed/19557161 Adiposity rs7826222 9.00E-09 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. NHGRI|-1
NM_003747 TNKS 19557161 http://www.ncbi.nlm.nih.gov/pubmed/19557161 Adiposity rs7826222 9.00E-09 Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution. NHGRI|-1
NM_007008 RTN4 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity (extreme) rs6726292 1.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_145650 MUC15 19553259 http://www.ncbi.nlm.nih.gov/pubmed/19553259 Obesity (extreme) rs12295638 4.00E-06 Common body mass index-associated variants confer risk of extreme obesity. NHGRI|-1
NM_005665 EVI5 19525955 http://www.ncbi.nlm.nih.gov/pubmed/19525955 Multiple sclerosis rs6604026 3.00E-06 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. NHGRI|-1
NM_005514 HLA-B 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple sclerosis rs2523393 1.00E-17 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_002124 HLA-DRB1 19525953 http://www.ncbi.nlm.nih.gov/pubmed/19525953 Multiple sclerosis rs3135388 4.00E-225 "Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci." NHGRI|-1
NM_006998 SCGN 19503597 http://www.ncbi.nlm.nih.gov/pubmed/19503597 Serum uric acid rs742132 9.00E-09 "Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations." NHGRI|-1
NM_005514 HLA-B 19483685 http://www.ncbi.nlm.nih.gov/pubmed/19483685 Drug-induced liver injury (flucloxacillin) rs2395029 9.00E-33 HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. NHGRI|-1
NM_177976 ARL6 19478329 http://www.ncbi.nlm.nih.gov/pubmed/19478329 Male infertility rs9814870 7.00E-07 Genome-wide study of single-nucleotide polymorphisms associated with azoospermia and severe oligozoospermia. NHGRI|-1
NM_006781 C6ORF10 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs2395148 7.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_006781 C6ORF10 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs3135363 7.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_006781 C6ORF10 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs2856683 7.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_006781 C6ORF10 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs9357152 7.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_019602 BTNL2 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs2395148 7.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_019602 BTNL2 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs3135363 7.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_019602 BTNL2 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs2856683 7.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_019602 BTNL2 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs9357152 7.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_002123 HLA-DQB1 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs2395148 7.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_002123 HLA-DQB1 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs3135363 7.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_002123 HLA-DQB1 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs2856683 7.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_002123 HLA-DQB1 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs9357152 7.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_006781 C6ORF10 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs2395148 1.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_006781 C6ORF10 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs3135363 1.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_006781 C6ORF10 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs2856683 1.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_006781 C6ORF10 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs9357152 1.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_019602 BTNL2 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs2395148 1.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_019602 BTNL2 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs3135363 1.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_019602 BTNL2 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs2856683 1.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_019602 BTNL2 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs9357152 1.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_002123 HLA-DQB1 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs2395148 1.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_002123 HLA-DQB1 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs3135363 1.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_002123 HLA-DQB1 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs2856683 1.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_002123 HLA-DQB1 19458352 http://www.ncbi.nlm.nih.gov/pubmed/19458352 Primary biliary cirrhosis rs9357152 1.00E-10 "Primary biliary cirrhosis associated with HLA, IL12A, and IL12RB2 variants." NHGRI|-1
NM_000655 SELL 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic lateral sclerosis rs3177980 4.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_001044722 CSNK1G3 19451621 http://www.ncbi.nlm.nih.gov/pubmed/19451621 Amyotrophic lateral sclerosis rs11241713 3.00E-06 Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis. NHGRI|-1
NM_004752 GCM2 19448621 http://www.ncbi.nlm.nih.gov/pubmed/19448621 Menarche and menopause (age at onset) rs2153157 5.00E-08 Genome-wide association studies identify loci associated with age at menarche and age at natural menopause. NHGRI|-1
NM_018112 TMEM38B 19448620 http://www.ncbi.nlm.nih.gov/pubmed/19448620 Menarche (age at onset) rs2090409 2.00E-09 Meta-analysis of genome-wide association data identifies two loci influencing age at menarche. NHGRI|-1
NM_080546 SLC44A1 19448620 http://www.ncbi.nlm.nih.gov/pubmed/19448620 Menarche (age at onset) rs2090409 2.00E-09 Meta-analysis of genome-wide association data identifies two loci influencing age at menarche. NHGRI|-1
NM_001079802 FKTN 19448620 http://www.ncbi.nlm.nih.gov/pubmed/19448620 Menarche (age at onset) rs2090409 2.00E-09 Meta-analysis of genome-wide association data identifies two loci influencing age at menarche. NHGRI|-1
NM_207647 FSD1L 19448620 http://www.ncbi.nlm.nih.gov/pubmed/19448620 Menarche (age at onset) rs2090409 2.00E-09 Meta-analysis of genome-wide association data identifies two loci influencing age at menarche. NHGRI|-1
NM_005421 TAL2 19448620 http://www.ncbi.nlm.nih.gov/pubmed/19448620 Menarche (age at onset) rs2090409 2.00E-09 Meta-analysis of genome-wide association data identifies two loci influencing age at menarche. NHGRI|-1
NM_032701 SUV420H2 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause (age at onset) rs1172822 6.00E-11 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_145735 ARHGEF7 19448619 http://www.ncbi.nlm.nih.gov/pubmed/19448619 Menopause (age at onset) rs7333181 3.00E-08 "Loci at chromosomes 13, 19 and 20 influence age at natural menopause." NHGRI|-1
NM_147147 BVES 19448622 http://www.ncbi.nlm.nih.gov/pubmed/19448622 Menarche (age at onset) rs314280 2.00E-14 Genome-wide association study identifies sequence variants on 6q21 associated with age at menarche. NHGRI|-1
NM_000417 IL2RA 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 Type 1 diabetes rs12251307 1.00E-13 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_207442 C14ORF181 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 Type 1 diabetes rs1465788 2.00E-12 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_139280 ORMDL3 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 Type 1 diabetes rs2290400 6.00E-13 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_001185098 INS 19430480 http://www.ncbi.nlm.nih.gov/pubmed/19430480 Type 1 diabetes rs7111341 4.00E-48 Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetes. NHGRI|-1
NM_181486 TBX5 19430479 http://www.ncbi.nlm.nih.gov/pubmed/19430479 Diastolic blood pressure rs2384550 4.00E-08 Genome-wide association study of blood pressure and hypertension. NHGRI|-1
NM_002634 PHB 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Diastolic blood pressure rs16948048 5.00E-09 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_178505 TMEM26 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Diastolic blood pressure rs1530440 1.00E-09 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_145307 RTKN2 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Diastolic blood pressure rs1530440 1.00E-09 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NR_024554 RHOBTB1 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Diastolic blood pressure rs1530440 1.00E-09 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_032199 ARID5B 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Diastolic blood pressure rs1530440 1.00E-09 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_005475 SH2B3 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Diastolic blood pressure rs653178 3.00E-18 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_152770 C4ORF22 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Diastolic blood pressure rs16998073 1.00E-21 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_000102 CYP17A1 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Systolic blood pressure rs11191548 7.00E-24 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_199077 CNNM2 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Systolic blood pressure rs11191548 7.00E-24 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_006460 HEXIM1 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Systolic blood pressure rs12946454 1.00E-08 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_001286 CLCN6 19430483 http://www.ncbi.nlm.nih.gov/pubmed/19430483 Systolic blood pressure rs17367504 2.00E-13 Genome-wide association study identifies eight loci associated with blood pressure. NHGRI|-1
NM_015475 FAM98A 19421330 http://www.ncbi.nlm.nih.gov/pubmed/19421330 Hypertension (young onset) rs9308945 3.00E-10 Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. NHGRI|-1
NM_015475 FAM98A 19421330 http://www.ncbi.nlm.nih.gov/pubmed/19421330 Hypertension (young onset) rs6711736 3.00E-10 Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. NHGRI|-1
NM_015475 FAM98A 19421330 http://www.ncbi.nlm.nih.gov/pubmed/19421330 Hypertension (young onset) rs6729869 3.00E-10 Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. NHGRI|-1
NM_015475 FAM98A 19421330 http://www.ncbi.nlm.nih.gov/pubmed/19421330 Hypertension (young onset) rs10495809 3.00E-10 Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. NHGRI|-1
NM_170672 RASGRP3 19421330 http://www.ncbi.nlm.nih.gov/pubmed/19421330 Hypertension (young onset) rs9308945 3.00E-10 Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. NHGRI|-1
NM_170672 RASGRP3 19421330 http://www.ncbi.nlm.nih.gov/pubmed/19421330 Hypertension (young onset) rs6711736 3.00E-10 Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. NHGRI|-1
NM_170672 RASGRP3 19421330 http://www.ncbi.nlm.nih.gov/pubmed/19421330 Hypertension (young onset) rs6729869 3.00E-10 Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. NHGRI|-1
NM_170672 RASGRP3 19421330 http://www.ncbi.nlm.nih.gov/pubmed/19421330 Hypertension (young onset) rs10495809 3.00E-10 Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. NHGRI|-1
NM_000402 G6PD 19419973 http://www.ncbi.nlm.nih.gov/pubmed/19419973 Bilirubin levels rs766420 9.00E-09 Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia. NHGRI|-1
NM_003157 NEK4 19416921 http://www.ncbi.nlm.nih.gov/pubmed/19416921 Bipolar disorder rs1042779 2.00E-07 Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry. NHGRI|-1
NM_000077 CDKN2A 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 Type 2 diabetes rs2383208 2.00E-29 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_004936 CDKN2B 19401414 http://www.ncbi.nlm.nih.gov/pubmed/19401414 Type 2 diabetes rs2383208 2.00E-29 Confirmation of multiple risk Loci and genetic impacts by a genome-wide association study of type 2 diabetes in the Japanese population. NHGRI|-1
NM_002389 CD46 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Biomedical quantitative traits rs12731740 3.00E-09 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_145902 HMGA1 19396169 http://www.ncbi.nlm.nih.gov/pubmed/19396169 Height rs6918981 3.00E-08 A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits. NHGRI|-1
NM_000908 NPR3 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Height rs10472828 3.00E-07 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001114634 PLAG1 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Height rs7815788 5.00E-06 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_005514 HLA-B 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Height rs13437082 5.00E-08 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NM_001177519 MICA 19343178 http://www.ncbi.nlm.nih.gov/pubmed/19343178 Height rs13437082 5.00E-08 Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. NHGRI|-1
NR_026554 CALCOCO1 19340012 http://www.ncbi.nlm.nih.gov/pubmed/19340012 Tanning rs7969151 2.00E-06 Genome-wide association study of tanning phenotype in a population of European ancestry. NHGRI|-1
NM_003059 SLC22A4 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs1016988 1.00E-12 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_002198 IRF1 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs1016988 1.00E-12 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_000508 FGA 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs6056 8.00E-39 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_000509 FGG 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs6056 8.00E-39 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_004252 SLC9A3R1 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs10512597 8.00E-11 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_015654 NAT9 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs10512597 8.00E-11 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_001122633 CPS1 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs7422339 9.00E-09 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_000565 IL6R 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs8192284 2.00E-11 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_003060 SLC22A5 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs10479002 1.00E-06 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_003059 SLC22A4 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs10479002 1.00E-06 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_002198 IRF1 20031577 http://www.ncbi.nlm.nih.gov/pubmed/20031577 Fibrinogen rs10479002 1.00E-06 "Novel loci, including those related to Crohn disease, psoriasis, and inflammation, identified in a genome-wide association study of fibrinogen in 17 686 women: the Women's Genome Health Study." NHGRI|-1
NM_181864 ACOT7 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 QT interval rs846111 1.00E-16 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_198681 PLEKHG5 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 QT interval rs846111 1.00E-16 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_002667 PLN 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 QT interval rs11756438 5.00E-22 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001130487 NDRG4 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 QT interval rs37062 3.00E-25 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_018231 SLC38A7 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 QT interval rs37062 3.00E-25 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_002080 GOT2 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 QT interval rs37062 3.00E-25 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_014153 ZC3H7A 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 QT interval rs8049607 5.00E-15 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_001192 TNFRSF17 19305408 http://www.ncbi.nlm.nih.gov/pubmed/19305408 QT interval rs8049607 5.00E-15 Common variants at ten loci influence QT interval duration in the QTGEN Study. NHGRI|-1
NM_000891 KCNJ2 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 QT interval rs17779747 6.00E-12 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_002667 PLN 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 QT interval rs11970286 2.00E-24 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_001130487 NDRG4 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 QT interval rs7188697 7.00E-25 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_002667 PLN 19305409 http://www.ncbi.nlm.nih.gov/pubmed/19305409 QT interval rs12210810 2.00E-17 Common variants at ten loci modulate the QT interval duration in the QTSCD Study. NHGRI|-1
NM_022475 HHIP 19300482 http://www.ncbi.nlm.nih.gov/pubmed/19300482 Chronic obstructive pulmonary disease rs1828591 1.00E-07 A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci. NHGRI|-1
NM_022475 HHIP 19300500 http://www.ncbi.nlm.nih.gov/pubmed/19300500 Pulmonary function measures rs13147758 8.00E-11 A genome-wide association study of pulmonary function measures in the Framingham Heart Study. NHGRI|-1
NM_001127501 ALPL 19303062 http://www.ncbi.nlm.nih.gov/pubmed/19303062 Folate pathway vitamin levels rs4654748 8.00E-18 "Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations." NHGRI|-1
NM_019111 HLA-DRA 19287509 http://www.ncbi.nlm.nih.gov/pubmed/19287509 Anti-cyclic Citrullinated Peptide Antibody rs1980493 5.00E-07 Genome-wide association study of determinants of anti-cyclic citrullinated peptide antibody titer in adults with rheumatoid arthritis. NHGRI|-1
NR_027317 C3ORF65 19247474 http://www.ncbi.nlm.nih.gov/pubmed/19247474 Smoking behavior rs6444087 9.00E-06 Genome-wide and candidate gene association study of cigarette smoking behaviors. NHGRI|-1
NM_001099405 SCN5A 19389651 http://www.ncbi.nlm.nih.gov/pubmed/19389651 Electrocardiographic conduction measures rs2070488 4.00E-06 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. NHGRI|-1
NM_002448 MSX1 19389651 http://www.ncbi.nlm.nih.gov/pubmed/19389651 Electrocardiographic conduction measures rs2008242 3.00E-06 Genome-wide association study of electrocardiographic conduction measures in an isolated founder population: Kosrae. NHGRI|-1
NM_033035 TSLP 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Plasma eosinophil count rs2416257 1.00E-06 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_001145662 GATA2 19198610 http://www.ncbi.nlm.nih.gov/pubmed/19198610 Plasma eosinophil count rs4857855 9.00E-17 Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. NHGRI|-1
NM_001005290 PSRC1 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial infarction (early onset) rs646776 8.00E-12 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_002959 SORT1 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial infarction (early onset) rs646776 8.00E-12 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_001195799 LDLR 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial infarction (early onset) rs1122608 2.00E-09 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_000077 CDKN2A 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial infarction (early onset) rs4977574 3.00E-44 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_004936 CDKN2B 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial infarction (early onset) rs4977574 3.00E-44 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_006933 SLC5A3 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial infarction (early onset) rs9982601 6.00E-11 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_032476 MRPS6 19198609 http://www.ncbi.nlm.nih.gov/pubmed/19198609 Myocardial infarction (early onset) rs9982601 6.00E-11 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. NHGRI|-1
NM_003317 NKX2-1 19198613 http://www.ncbi.nlm.nih.gov/pubmed/19198613 Thyroid cancer rs944289 2.00E-09 Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations. NHGRI|-1
NM_212550 BLOC1S3 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Quantitative traits rs2159324 4.00E-07 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_005713 COL4A3BP 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Quantitative traits rs3846663 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_212550 BLOC1S3 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Quantitative traits rs2159324 2.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_002014 FKBP4 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Quantitative traits rs10848704 2.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001128916 TOMM40 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Quantitative traits rs4420638 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001646 APOC4 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Quantitative traits rs4420638 5.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001128916 TOMM40 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Quantitative traits rs4420638 3.00E-07 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001646 APOC4 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Quantitative traits rs4420638 3.00E-07 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_005713 COL4A3BP 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Quantitative traits rs3846663 6.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_054033 FKBP1B 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Quantitative traits rs7561273 6.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_016481 C9ORF156 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Quantitative traits rs755109 1.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001128916 TOMM40 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Quantitative traits rs4420638 2.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_001646 APOC4 19197348 http://www.ncbi.nlm.nih.gov/pubmed/19197348 Quantitative traits rs4420638 2.00E-06 Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae. NHGRI|-1
NM_016441 CRIM1 19260139 http://www.ncbi.nlm.nih.gov/pubmed/19260139 Anthropometric traits rs1863080 8.00E-06 "Genome-wide association study of anthropometric traits in Korcula Island, Croatia." NHGRI|-1
NM_014669 NUP93 20031564 http://www.ncbi.nlm.nih.gov/pubmed/20031564 HDL cholesterol rs1800775 4.00E-93 "Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study." NHGRI|-1
NM_001126108 SLC12A3 20031564 http://www.ncbi.nlm.nih.gov/pubmed/20031564 HDL cholesterol rs1800775 4.00E-93 "Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study." NHGRI|-1
NM_014685 HERPUD1 20031564 http://www.ncbi.nlm.nih.gov/pubmed/20031564 HDL cholesterol rs1800775 4.00E-93 "Polymorphism in the CETP gene region, HDL cholesterol, and risk of future myocardial infarction: Genomewide analysis among 18 245 initially healthy women from the Women's Genome Health Study." NHGRI|-1
NM_015236 LPHN3 19260141 http://www.ncbi.nlm.nih.gov/pubmed/19260141 Biochemical measures rs4599440 2.00E-06 "Genome-wide association study of biochemical traits in Korcula Island, Croatia." NHGRI|-1
NM_001166598 APOA5 19185284 http://www.ncbi.nlm.nih.gov/pubmed/19185284 Plasma carotenoid and tocopherol levels rs12272004 8.00E-10 "Common variation in the beta-carotene 15,15'-monooxygenase 1 gene affects circulating levels of carotenoids: a genome-wide association study." NHGRI|-1
NM_002117 HLA-C 19169254 http://www.ncbi.nlm.nih.gov/pubmed/19169254 Psoriasis rs12191877 1.00E-100 Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways. NHGRI|-1
NR_026554 CALCOCO1 19165232 http://www.ncbi.nlm.nih.gov/pubmed/19165232 Panic disorder rs941184 3.00E-07 Genome-wide association study of panic disorder in the Japanese population. NHGRI|-1
NM_018402 IL26 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 Ulcerative colitis rs1558744 3.00E-12 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_019602 BTNL2 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 Ulcerative colitis rs2395185 1.00E-16 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_019111 HLA-DRA 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 Ulcerative colitis rs2395185 1.00E-16 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_002124 HLA-DRB1 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 Ulcerative colitis rs2395185 1.00E-16 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_002122 HLA-DQA1 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 Ulcerative colitis rs2395185 1.00E-16 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_002123 HLA-DQB1 19122664 http://www.ncbi.nlm.nih.gov/pubmed/19122664 Ulcerative colitis rs2395185 1.00E-16 Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. NHGRI|-1
NM_025236 RNF39 19115949 http://www.ncbi.nlm.nih.gov/pubmed/19115949 AIDS progression rs8321 5.00E-07 Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). NHGRI|-1
NM_005931 MICB 19115949 http://www.ncbi.nlm.nih.gov/pubmed/19115949 AIDS progression rs2395029 3.00E-19 Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). NHGRI|-1
NM_001011700 MCCD1 19115949 http://www.ncbi.nlm.nih.gov/pubmed/19115949 AIDS progression rs2395029 3.00E-19 Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). NHGRI|-1
NM_002341 LTB 19115949 http://www.ncbi.nlm.nih.gov/pubmed/19115949 AIDS progression rs2395029 3.00E-19 Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). NHGRI|-1
NM_000594 TNF 19115949 http://www.ncbi.nlm.nih.gov/pubmed/19115949 AIDS progression rs2395029 3.00E-19 Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). NHGRI|-1
NM_002117 HLA-C 19115949 http://www.ncbi.nlm.nih.gov/pubmed/19115949 AIDS progression rs10484554 6.00E-08 Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). NHGRI|-1
NM_001759 CCND2 19107115 http://www.ncbi.nlm.nih.gov/pubmed/19107115 Major depressive disorder rs4238010 6.00E-06 Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts. NHGRI|-1
NM_001063 TF 19084217 http://www.ncbi.nlm.nih.gov/pubmed/19084217 Serum markers of iron status rs1867504 2.00E-06 Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels. NHGRI|-1
NM_000039 APOA1 19074352 http://www.ncbi.nlm.nih.gov/pubmed/19074352 Triglycerides rs10892151 3.00E-29 A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. NHGRI|-1
NM_000040 APOC3 19074352 http://www.ncbi.nlm.nih.gov/pubmed/19074352 Triglycerides rs10892151 3.00E-29 A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. NHGRI|-1
NM_000482 APOA4 19074352 http://www.ncbi.nlm.nih.gov/pubmed/19074352 Triglycerides rs10892151 3.00E-29 A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. NHGRI|-1
NM_001166598 APOA5 19074352 http://www.ncbi.nlm.nih.gov/pubmed/19074352 Triglycerides rs10892151 3.00E-29 A null mutation in human APOC3 confers a favorable plasma lipid profile and apparent cardioprotection. NHGRI|-1
NM_001122740 ESR1 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone mineral density (hip) rs1038304 4.00E-10 New sequence variants associated with bone mineral density. NHGRI|-1
NM_002334 LRP4 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone mineral density (hip) rs1007738 7.00E-07 New sequence variants associated with bone mineral density. NHGRI|-1
NM_001122740 ESR1 19079262 http://www.ncbi.nlm.nih.gov/pubmed/19079262 Bone mineral density (spine) rs6929137 2.00E-10 New sequence variants associated with bone mineral density. NHGRI|-1
NM_012306 FAIM2 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body mass index rs7138803 1.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_004841 RASAL2 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body mass index rs10913469 6.00E-08 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001127895 CHST8 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body mass index rs29941 7.00E-12 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170734 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body mass index rs925946 9.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_173201 ATP2A1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body mass index rs7498665 3.00E-10 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170734 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Body mass index rs7481311 8.00E-06 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170734 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Weight rs925946 4.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_001127895 CHST8 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Weight rs29941 5.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_173201 ATP2A1 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Weight rs7498665 1.00E-09 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_012306 FAIM2 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Weight rs7138803 2.00E-07 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_170734 BDNF 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Weight rs7481311 3.00E-06 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_004841 RASAL2 19079260 http://www.ncbi.nlm.nih.gov/pubmed/19079260 Weight rs10913469 1.00E-08 Genome-wide association yields new sequence variants at seven loci that associate with measures of obesity. NHGRI|-1
NM_173808 NEGR1 19079261 http://www.ncbi.nlm.nih.gov/pubmed/19079261 Body mass index rs2815752 6.00E-08 Six new loci associated with body mass index highlight a neuronal influence on body weight regulation. NHGRI|-1
NM_007029 STMN2 19081515 http://www.ncbi.nlm.nih.gov/pubmed/19081515 Creutzfeldt-Jakob disease rs1460163 6.00E-08 Genetic risk factors for variant Creutzfeldt-Jakob disease: a genome-wide association study. NHGRI|-1
NM_004386 NCAN 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, total" rs2304130 2.00E-15 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_021727 FADS3 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, total" rs174570 2.00E-10 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000039 APOA1 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, total" rs12272004 7.00E-07 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000482 APOA4 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, total" rs12272004 7.00E-07 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001166598 APOA5 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, total" rs12272004 7.00E-07 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000040 APOC3 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 "Cholesterol, total" rs12272004 7.00E-07 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_021727 FADS3 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 HDL cholesterol rs174570 4.00E-06 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_130470 MADD 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 HDL cholesterol rs7395662 6.00E-11 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_004476 FOLH1 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 HDL cholesterol rs7395662 6.00E-11 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_006565 CTCF 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 HDL cholesterol rs2271293 8.00E-16 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_019854 PRMT8 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 HDL cholesterol rs2271293 8.00E-16 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_021727 FADS3 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 LDL cholesterol rs174570 4.00E-13 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000039 APOA1 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 LDL cholesterol rs12272004 5.00E-13 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000482 APOA4 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 LDL cholesterol rs12272004 5.00E-13 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001166598 APOA5 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 LDL cholesterol rs12272004 5.00E-13 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000040 APOC3 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 LDL cholesterol rs12272004 5.00E-13 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_004386 NCAN 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 LDL cholesterol rs2304130 3.00E-06 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_001128916 TOMM40 19060911 http://www.ncbi.nlm.nih.gov/pubmed/19060911 Triglycerides rs439401 2.00E-09 Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts. NHGRI|-1
NM_000039 APOA1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 HDL cholesterol rs964184 1.00E-12 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000040 APOC3 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 HDL cholesterol rs964184 1.00E-12 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000482 APOA4 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 HDL cholesterol rs964184 1.00E-12 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001166598 APOA5 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 HDL cholesterol rs964184 1.00E-12 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_004265 FADS2 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 HDL cholesterol rs174547 2.00E-12 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_021727 FADS3 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 HDL cholesterol rs174547 2.00E-12 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_139314 ANGPTL4 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 HDL cholesterol rs2967605 1.00E-08 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_004386 NCAN 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 LDL cholesterol rs10401969 2.00E-08 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_153221 CILP2 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 LDL cholesterol rs10401969 2.00E-08 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001005290 PSRC1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 LDL cholesterol rs12740374 2.00E-42 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_002959 SORT1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 LDL cholesterol rs12740374 2.00E-42 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000545 HNF1A 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 LDL cholesterol rs2650000 2.00E-08 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001646 APOC4 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 LDL cholesterol rs4420638 4.00E-27 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_014495 ANGPTL3 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs10889353 3.00E-07 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_054028 AMAC1L2 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs7819412 3.00E-08 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_004265 FADS2 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs174547 2.00E-14 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_021727 FADS3 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs174547 2.00E-14 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000039 APOA1 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs964184 4.00E-62 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000040 APOC3 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs964184 4.00E-62 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_000482 APOA4 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs964184 4.00E-62 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001166598 APOA5 19060906 http://www.ncbi.nlm.nih.gov/pubmed/19060906 Triglycerides rs964184 4.00E-62 Common variants at 30 loci contribute to polygenic dyslipidemia. NHGRI|-1
NM_001005290 PSRC1 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 LDL cholesterol rs646776 2.00E-12 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_002959 SORT1 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 LDL cholesterol rs646776 2.00E-12 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_004265 FADS2 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 LDL cholesterol rs174546 1.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_016269 LEF1 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Other metabolic traits rs2650000 3.00E-11 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_002303 LEPR 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Other metabolic traits rs12753193 4.00E-07 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_003742 ABCB11 19060910 http://www.ncbi.nlm.nih.gov/pubmed/19060910 Other metabolic traits rs560887 6.00E-10 Genome-wide association analysis of metabolic traits in a birth cohort from a founder population. NHGRI|-1
NM_004936 CDKN2B 19056611 http://www.ncbi.nlm.nih.gov/pubmed/19056611 Type 2 diabetes rs10811661 7.00E-07 Adiposity-related heterogeneity in patterns of type 2 diabetes susceptibility observed in genome-wide association data. NHGRI|-1
NM_013256 ZNF180 18957941 http://www.ncbi.nlm.nih.gov/pubmed/18957941 Personality dimensions rs644148 8.00E-06 Genome-wide association scan for five major dimensions of personality. NHGRI|-1
NM_013256 ZNF180 18957941 http://www.ncbi.nlm.nih.gov/pubmed/18957941 Personality dimensions rs644148 9.00E-07 Genome-wide association scan for five major dimensions of personality. NHGRI|-1
NM_002941 ROBO1 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Brain imaging in schizophrenia (interaction) rs9836484 4.00E-06 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_001046 SLC12A2 19023125 http://www.ncbi.nlm.nih.gov/pubmed/19023125 Brain imaging in schizophrenia (interaction) rs245201 9.00E-08 A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype. NHGRI|-1
NM_000751 CHRND 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Brain lesion load rs2602397 4.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_003412 ZIC1 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple sclerosis rs1841770 8.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_018155 SLC25A36 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple sclerosis rs908821 3.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_004973 JARID2 19010793 http://www.ncbi.nlm.nih.gov/pubmed/19010793 Multiple sclerosis (severity) rs6941421 6.00E-06 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. NHGRI|-1
NM_022454 SOX17 18997786 http://www.ncbi.nlm.nih.gov/pubmed/18997786 Intracranial aneurysm rs9298506 2.00E-09 Susceptibility loci for intracranial aneurysm in European and Japanese populations. NHGRI|-1
NM_000077 CDKN2A 18997786 http://www.ncbi.nlm.nih.gov/pubmed/18997786 Intracranial aneurysm rs1333040 1.00E-10 Susceptibility loci for intracranial aneurysm in European and Japanese populations. NHGRI|-1
NM_004936 CDKN2B 18997786 http://www.ncbi.nlm.nih.gov/pubmed/18997786 Intracranial aneurysm rs1333040 1.00E-10 Susceptibility loci for intracranial aneurysm in European and Japanese populations. NHGRI|-1
NM_006226 PLCL1 18997786 http://www.ncbi.nlm.nih.gov/pubmed/18997786 Intracranial aneurysm rs700651 4.00E-08 Susceptibility loci for intracranial aneurysm in European and Japanese populations. NHGRI|-1
NM_001347 DGKQ 18985386 http://www.ncbi.nlm.nih.gov/pubmed/18985386 Parkinson's disease (familial) rs1564282 7.00E-07 Genomewide association study for susceptibility genes contributing to familial Parkinson disease. NHGRI|-1
NM_000417 IL2RA 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 Type 1 diabetes rs12251307 2.00E-06 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_006257 PRKCQ 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 Type 1 diabetes rs947474 4.00E-09 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_152308 C16ORF75 18978792 http://www.ncbi.nlm.nih.gov/pubmed/18978792 Type 1 diabetes rs416603 3.00E-06 Meta-analysis of genome-wide association study data identifies additional type 1 diabetes risk loci. NHGRI|-1
NM_198253 TERT 18978790 http://www.ncbi.nlm.nih.gov/pubmed/18978790 Lung cancer rs402710 4.00E-06 Lung cancer susceptibility locus at 5p15.33. NHGRI|-1
NM_130847 AMOTL1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention deficit hyperactivity disorder and conduct disorder rs10831284 2.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_005603 ATP8B1 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention deficit hyperactivity disorder and conduct disorder rs7236632 6.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_014761 KIAA0174 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention deficit hyperactivity disorder and conduct disorder rs16973500 7.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001361 DHODH 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention deficit hyperactivity disorder and conduct disorder rs16973500 7.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_015101 GLT25D2 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention deficit hyperactivity disorder and conduct disorder rs10797919 9.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_032859 ABHD13 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention deficit hyperactivity disorder and conduct disorder rs10492664 1.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001100873 C16ORF46 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention deficit hyperactivity disorder and conduct disorder rs4889240 7.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001004341 ETV3L 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention deficit hyperactivity disorder and conduct disorder rs6427356 8.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_001145312 ETV3 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention deficit hyperactivity disorder and conduct disorder rs6427356 8.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_003507 FZD7 18951430 http://www.ncbi.nlm.nih.gov/pubmed/18951430 Attention deficit hyperactivity disorder and conduct disorder rs1521882 8.00E-06 Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study. NHGRI|-1
NM_002124 HLA-DRB1 18941528 http://www.ncbi.nlm.nih.gov/pubmed/18941528 Multiple sclerosis rs3129934 9.00E-11 "Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms." NHGRI|-1
NM_012387 PADI4 18849993 http://www.ncbi.nlm.nih.gov/pubmed/18849993 Basal cell carcinoma (cutaneous) rs7538876 4.00E-12 Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits. NHGRI|-1
NM_018125 ARHGEF10L 18849993 http://www.ncbi.nlm.nih.gov/pubmed/18849993 Basal cell carcinoma (cutaneous) rs7538876 4.00E-12 Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traits. NHGRI|-1
NM_002885 RAP1GAP 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Plasma levels of liver enzymes rs1780324 7.00E-15 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_000545 HNF1A 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Plasma levels of liver enzymes rs1169313 2.00E-10 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_015380 SAMM50 18940312 http://www.ncbi.nlm.nih.gov/pubmed/18940312 Plasma levels of liver enzymes rs2281135 8.00E-16 Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes. NHGRI|-1
NM_019111 HLA-DRA 18836448 http://www.ncbi.nlm.nih.gov/pubmed/18836448 Ulcerative colitis rs9268877 6.00E-18 "Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility." NHGRI|-1
NM_019602 BTNL2 18836448 http://www.ncbi.nlm.nih.gov/pubmed/18836448 Ulcerative colitis rs9268877 6.00E-18 "Sequence variants in IL10, ARPC2 and multiple other loci contribute to ulcerative colitis susceptibility." NHGRI|-1
NM_001128916 TOMM40 18823527 http://www.ncbi.nlm.nih.gov/pubmed/18823527 Alzheimer's disease rs6859 6.00E-14 A genome-wide association study for late-onset Alzheimer's disease using DNA pooling. NHGRI|-1
NM_001646 APOC4 18802019 http://www.ncbi.nlm.nih.gov/pubmed/18802019 LDL cholesterol rs4420638 2.00E-07 Common SNPs in HMGCR in micronesians and whites associated with LDL-cholesterol levels affect alternative splicing of exon13. NHGRI|-1
NM_006257 PRKCQ 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 Rheumatoid arthritis rs4750316 4.00E-06 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_002124 HLA-DRB1 18794853 http://www.ncbi.nlm.nih.gov/pubmed/18794853 Rheumatoid arthritis rs6457620 4.00E-186 Common variants at CD40 and other loci confer risk of rheumatoid arthritis. NHGRI|-1
NM_017491 WDR1 18759275 http://www.ncbi.nlm.nih.gov/pubmed/18759275 Serum uric acid rs16890979 1.00E-11 Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish. NHGRI|-1
NM_080424 SP110 18758461 http://www.ncbi.nlm.nih.gov/pubmed/18758461 Chronic lymphocytic leukemia rs13397985 6.00E-10 A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia. NHGRI|-1
NM_003720 PSMG1 18758464 http://www.ncbi.nlm.nih.gov/pubmed/18758464 Inflammatory bowel disease rs2836878 4.00E-12 Loci on 20q13 and 21q22 are associated with pediatric-onset inflammatory bowel disease. NHGRI|-1
NM_002122 HLA-DQA1 18668548 http://www.ncbi.nlm.nih.gov/pubmed/18668548 Rheumatoid arthritis rs6457617 1.00E-09 Genome-wide association study of rheumatoid arthritis in the Spanish population: KLF12 as a risk locus for rheumatoid arthritis susceptibility. NHGRI|-1
NM_020124 IFNK 18615156 http://www.ncbi.nlm.nih.gov/pubmed/18615156 Response to TNF antagonist treatment rs7046653 5.00E-07 Genome-wide association scan identifies candidate polymorphisms associated with differential response to anti-TNF treatment in rheumatoid arthritis. NHGRI|-1
NM_006530 YEATS4 18591461 http://www.ncbi.nlm.nih.gov/pubmed/18591461 Response to diuretic therapy rs317689 3.00E-07 Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diuretic. NHGRI|-1
NM_006530 YEATS4 18591461 http://www.ncbi.nlm.nih.gov/pubmed/18591461 Response to diuretic therapy rs315135 3.00E-07 Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diuretic. NHGRI|-1
NM_006530 YEATS4 18591461 http://www.ncbi.nlm.nih.gov/pubmed/18591461 Response to diuretic therapy rs7297610 3.00E-07 Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diuretic. NHGRI|-1
NM_006654 FRS2 18591461 http://www.ncbi.nlm.nih.gov/pubmed/18591461 Response to diuretic therapy rs317689 3.00E-07 Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diuretic. NHGRI|-1
NM_006654 FRS2 18591461 http://www.ncbi.nlm.nih.gov/pubmed/18591461 Response to diuretic therapy rs315135 3.00E-07 Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diuretic. NHGRI|-1
NM_006654 FRS2 18591461 http://www.ncbi.nlm.nih.gov/pubmed/18591461 Response to diuretic therapy rs7297610 3.00E-07 Genomic association analysis suggests chromosome 12 locus influencing antihypertensive response to thiazide diuretic. NHGRI|-1
NM_139280 ORMDL3 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn's disease rs2872507 5.00E-09 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_031409 CCR6 18587394 http://www.ncbi.nlm.nih.gov/pubmed/18587394 Crohn's disease rs2301436 1.00E-12 Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. NHGRI|-1
NM_002124 HLA-DRB1 18576341 http://www.ncbi.nlm.nih.gov/pubmed/18576341 Arthritis (juvenile idiopathic) rs2395148 2.00E-10 Association of the TRAF1-C5 locus on chromosome 9 with juvenile idiopathic arthritis. NHGRI|-1
NM_206824 VKORC1 18535201 http://www.ncbi.nlm.nih.gov/pubmed/18535201 Warfarin maintenance dose rs10871454 5.00E-34 A genome-wide scan for common genetic variants with a large influence on warfarin maintenance dose. NHGRI|-1
NM_001562 IL18 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Protein quantitative trait loci rs2250417 7.00E-13 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_002941 ROBO1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Protein quantitative trait loci rs9834373 4.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_002117 HLA-C 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Protein quantitative trait loci rs9461688 4.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_018112 TMEM38B 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Protein quantitative trait loci rs4742971 8.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_198827 GPR133 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Protein quantitative trait loci rs10466868 1.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001146279 SHBG 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Protein quantitative trait loci rs6761 3.00E-07 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_173843 IL1RN 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Protein quantitative trait loci rs6761276 7.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_016623 FAM49B 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Protein quantitative trait loci rs10092658 6.00E-06 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_006041 HS3ST3B1 18464913 http://www.ncbi.nlm.nih.gov/pubmed/18464913 Protein quantitative trait loci rs3848445 8.00E-09 A genome-wide association study identifies protein quantitative trait loci (pQTLs). NHGRI|-1
NM_001122740 ESR1 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone mineral density (hip) rs4870044 2.00E-07 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_001122740 ESR1 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone mineral density (hip) rs1038304 5.00E-09 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_025059 C6ORF97 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone mineral density (spine) rs1999805 2.00E-08 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_001122740 ESR1 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone mineral density (spine) rs4870044 2.00E-11 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_001122740 ESR1 18445777 http://www.ncbi.nlm.nih.gov/pubmed/18445777 Bone mineral density (spine) rs1038304 4.00E-11 Multiple genetic loci for bone mineral density and fractures. NHGRI|-1
NM_000565 IL6R 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-reactive protein rs8192284 2.00E-08 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_002303 LEPR 18439548 http://www.ncbi.nlm.nih.gov/pubmed/18439548 C-reactive protein rs1892534 7.00E-21 "Loci related to metabolic-syndrome pathways including LEPR,HNF1A, IL6R, and GCKR associate with plasma C-reactive protein: the Women's Genome Health Study." NHGRI|-1
NM_012335 MYO1F 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs7249094 1.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_032152 PRAM1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs7249094 1.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_022346 NCAPG 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs6830062 1.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_015245 ANKS1A 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs4713858 4.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_018679 TCP11 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs4713858 4.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003427 ZNF76 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs4713858 4.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_024831 TGS1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs10958476 7.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001135690 PENK 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs10958476 7.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_024721 ZFHX4 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs7846385 5.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001099432 BCAS3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs757608 6.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_005994 TBX2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs757608 6.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001035256 POMC 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs6733301 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_153759 DNMT3A 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs6733301 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_021907 DTNB 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs6733301 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_017521 FEV 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs1052483 1.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_144712 SLC23A3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs1052483 1.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001201 BMP3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs710841 2.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_006366 CAP2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs12199222 7.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001105568 KIF13A 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs12199222 7.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001024630 RUNX2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs9395066 8.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_020771 HACE1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs314268 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_147147 BVES 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs314268 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001142403 CD164 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs9487094 4.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_006717 SPIN1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs2814828 9.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001145945 SLCO1C1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs11611208 2.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_019844 SLCO1B3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs11611208 2.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003647 DGKE 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs4794665 1.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_005082 TRIM25 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs4794665 1.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_004645 COIL 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs4794665 1.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001017373 SAMD3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs6899976 6.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_002073 GNAZ 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs5751614 6.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_014433 RTDR1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs5751614 6.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_152855 IGLL1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs5751614 6.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_004993 ATXN3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs7153027 1.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_017437 CPSF2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs7153027 1.00E-10 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_015986 CRLF3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs3760318 2.00E-09 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_024857 ATAD5 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs3760318 2.00E-09 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_032933 C18ORF45 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs4800148 4.00E-09 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_022730 COPS7B 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs749052 1.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_002601 PDE6D 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs749052 1.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NR_036052 PTMA 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs749052 1.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_032151 PCBD2 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs31198 8.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_178019 CATSPER3 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs31198 8.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_001745 CAMLG 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs31198 8.00E-06 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_033109 PNPT1 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs3791679 6.00E-11 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_030915 LBH 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs1776897 1.00E-08 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_172177 MRPL42 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs3825199 2.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_003348 UBE2N 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs3825199 2.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_005153 USP10 18391951 http://www.ncbi.nlm.nih.gov/pubmed/18391951 Height rs2326458 8.00E-07 Many sequence variants affecting diversity of adult human height. NHGRI|-1
NM_002181 IHH 18391952 http://www.ncbi.nlm.nih.gov/pubmed/18391952 Height rs6724465 2.00E-08 Genome-wide association analysis identifies 20 loci that influence adult height. NHGRI|-1
NM_002117 HLA-C 18369459 http://www.ncbi.nlm.nih.gov/pubmed/18369459 Psoriasis rs2395029 2.00E-26 A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. NHGRI|-1
NM_002117 HLA-C 18369459 http://www.ncbi.nlm.nih.gov/pubmed/18369459 Psoriasis rs10484554 2.00E-39 A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci. NHGRI|-1
NR_034154 C11ORF92 18372901 http://www.ncbi.nlm.nih.gov/pubmed/18372901 Colorectal cancer rs3802842 6.00E-10 Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21. NHGRI|-1
NM_003178 SYN2 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 Type 2 diabetes rs17036101 2.00E-07 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_138712 PPARG 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 Type 2 diabetes rs17036101 2.00E-07 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_021794 ADAM30 18372903 http://www.ncbi.nlm.nih.gov/pubmed/18372903 Type 2 diabetes rs10923931 4.00E-08 Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. NHGRI|-1
NM_002117 HLA-C 18364390 http://www.ncbi.nlm.nih.gov/pubmed/18364390 Psoriasis rs3134792 1.00E-09 Identification of ZNF313/RNF114 as a novel psoriasis susceptibility gene. NHGRI|-1
NM_001011552 SLC9A4 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac disease rs13015714 4.00E-09 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_001295 CCR1 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac disease rs6441961 3.00E-07 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_005475 SH2B3 18311140 http://www.ncbi.nlm.nih.gov/pubmed/18311140 Celiac disease rs653178 8.00E-08 Newly identified genetic risk variants for celiac disease related to the immune response. NHGRI|-1
NM_153183 NUDT10 18264097 http://www.ncbi.nlm.nih.gov/pubmed/18264097 Prostate cancer rs5945619 2.00E-09 Multiple newly identified loci associated with prostate cancer susceptibility. NHGRI|-1
NM_153183 NUDT10 18264098 http://www.ncbi.nlm.nih.gov/pubmed/18264098 Prostate cancer rs5945572 4.00E-13 Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. NHGRI|-1
NM_001005332 MAGED1 18264098 http://www.ncbi.nlm.nih.gov/pubmed/18264098 Prostate cancer rs5945572 4.00E-13 Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer. NHGRI|-1
NM_000518 HBB 18245381 http://www.ncbi.nlm.nih.gov/pubmed/18245381 Fetal hemoglobin levels rs4910742 1.00E-21 Genome-wide association study shows BCL11A associated with persistent fetal hemoglobin and amelioration of the phenotype of beta-thalassemia. NHGRI|-1
NM_001145808 ITGAM 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 Systemic lupus erythematosus rs11574637 3.00E-11 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_004232 SOCS6 18204098 http://www.ncbi.nlm.nih.gov/pubmed/18204098 Systemic lupus erythematosus rs17083844 6.00E-06 Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. NHGRI|-1
NM_002868 RAB5B 18198356 http://www.ncbi.nlm.nih.gov/pubmed/18198356 Type 1 diabetes rs1701704 9.00E-10 A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study. NHGRI|-1
NM_001982 ERBB3 18198356 http://www.ncbi.nlm.nih.gov/pubmed/18198356 Type 1 diabetes rs1701704 9.00E-10 A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study. NHGRI|-1
NM_001798 CDK2 18198356 http://www.ncbi.nlm.nih.gov/pubmed/18198356 Type 1 diabetes rs1701704 9.00E-10 A novel susceptibility locus for type 1 diabetes on Chr12q13 identified by a genome-wide association study. NHGRI|-1
NM_001646 APOC4 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 LDL cholesterol rs4420638 1.00E-60 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_014495 ANGPTL3 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs12130333 2.00E-08 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_033407 DOCK7 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs12130333 2.00E-08 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_000039 APOA1 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs28927680 2.00E-17 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_000040 APOC3 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs28927680 2.00E-17 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_000482 APOA4 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs28927680 2.00E-17 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_001166598 APOA5 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs28927680 2.00E-17 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_003904 ZNF259 18193044 http://www.ncbi.nlm.nih.gov/pubmed/18193044 Triglycerides rs28927680 2.00E-17 "Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans." NHGRI|-1
NM_001142324 SLC18A1 18193046 http://www.ncbi.nlm.nih.gov/pubmed/18193046 Triglycerides rs326 5.00E-12 Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. NHGRI|-1
NM_003782 B3GALT4 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 LDL cholesterol rs2254287 5.00E-08 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001166598 APOA5 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs12286037 1.00E-26 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_000482 APOA4 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs12286037 1.00E-26 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_000040 APOC3 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs12286037 1.00E-26 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_000039 APOA1 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs12286037 1.00E-26 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_014495 ANGPTL3 18193043 http://www.ncbi.nlm.nih.gov/pubmed/18193043 Triglycerides rs1748195 2.00E-10 Newly identified loci that influence lipid concentrations and risk of coronary artery disease. NHGRI|-1
NM_001130675 CLGN 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Select biomarker traits rs17532515 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_153702 ELMOD2 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Select biomarker traits rs17532515 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_006504 PTPRE 17903293 http://www.ncbi.nlm.nih.gov/pubmed/17903293 Select biomarker traits rs2387326 1.00E-06 Genome-wide association with select biomarker traits in the Framingham Heart Study. NHGRI|-1
NM_015576 ERC2 17903296 http://www.ncbi.nlm.nih.gov/pubmed/17903296 Hip geometry rs2054989 6.00E-07 Genome-wide association with bone mass and geometry in the Framingham Heart Study. NHGRI|-1
NM_018330 KIAA1598 17903304 http://www.ncbi.nlm.nih.gov/pubmed/17903304 Heart failure rs740363 9.00E-06 Framingham Heart Study 100K project: genome-wide associations for cardiovascular disease outcomes. NHGRI|-1
NM_178821 WDR69 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Blood pressure rs7591163 3.00E-07 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_005708 GPC6 17903302 http://www.ncbi.nlm.nih.gov/pubmed/17903302 Tonometry rs6492654 2.00E-06 Framingham Heart Study 100K Project: genome-wide associations for blood pressure and arterial stiffness. NHGRI|-1
NM_001006939 LRRC18 17903303 http://www.ncbi.nlm.nih.gov/pubmed/17903303 Subclinical atherosclerosis traits (other) rs3849150 2.00E-06 Genome-wide association study for subclinical atherosclerosis in major arterial territories in the NHLBI's Framingham Heart Study. NHGRI|-1
NM_001112732 MCF2L 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Factor VII rs561241 5.00E-16 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_000504 F10 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Factor VII rs561241 5.00E-16 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_003891 PROZ 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Factor VII rs561241 5.00E-16 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_001004730 OR5AR1 17903294 http://www.ncbi.nlm.nih.gov/pubmed/17903294 Hemostatic factors and hematological phenotypes rs1397048 7.00E-08 Genome-wide association and linkage analyses of hemostatic factors and hematological phenotypes in the Framingham Heart Study. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs11209003 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs11209002 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs2064689 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs1004819 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs2902440 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs11465802 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs2201841 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs11465804 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs11209026 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs1343151 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs10889676 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs10889677 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs9988642 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs12567232 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs6669582 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs10789230 1.00E-08 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs11209003 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs11209002 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs2064689 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs1004819 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs2902440 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs11465802 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs2201841 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs11465804 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs11209026 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs1343151 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs10889676 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs10889677 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs9988642 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs12567232 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs6669582 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_144701 IL23R 17804789 http://www.ncbi.nlm.nih.gov/pubmed/17804789 Crohn's disease rs10789230 2.00E-07 Genome-wide association study for Crohn's disease in the Quebec Founder Population identifies multiple validated disease loci. NHGRI|-1
NM_000518 HBB 17767159 http://www.ncbi.nlm.nih.gov/pubmed/17767159 F-cell distribution NR 2.00E-38 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15. NHGRI|-1
NM_139280 ORMDL3 17611496 http://www.ncbi.nlm.nih.gov/pubmed/17611496 Asthma rs7216389 9.00E-11 Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma. NHGRI|-1
NM_001185098 INS 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 Type 1 diabetes rs1004446 4.00E-09 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NR_028043 IGF2AS 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 Type 1 diabetes rs1004446 4.00E-09 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NM_002124 HLA-DRB1 17632545 http://www.ncbi.nlm.nih.gov/pubmed/17632545 Type 1 diabetes rs2647044 1.00E-16 A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. NHGRI|-1
NM_020998 MST1 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Crohn's disease rs9858542 4.00E-08 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_002834 PTPN11 17554300 http://www.ncbi.nlm.nih.gov/pubmed/17554300 Type 1 diabetes rs6679677 5.00E-26 "Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls." NHGRI|-1
NM_020998 MST1 17554261 http://www.ncbi.nlm.nih.gov/pubmed/17554261 Crohn's disease rs9858542 5.00E-08 Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility. NHGRI|-1
NM_006608 PHTF1 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 Type 1 diabetes rs6679677 8.00E-24 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_001185098 INS 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 Type 1 diabetes rs3741208 2.00E-07 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NR_028043 IGF2AS 17554260 http://www.ncbi.nlm.nih.gov/pubmed/17554260 Type 1 diabetes rs3741208 2.00E-07 Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes. NHGRI|-1
NM_002124 HLA-DRB1 17505501 http://www.ncbi.nlm.nih.gov/pubmed/17505501 Response to ximelagatran treatment NR 9.00E-06 Genome-wide pharmacogenetic investigation of a hepatic adverse event without clinical signs of immunopathology suggests an underlying immune pathogenesis. NHGRI|-1
NM_000077 CDKN2A 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 Type 2 diabetes rs564398 1.00E-06 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_004936 CDKN2B 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 Type 2 diabetes rs564398 1.00E-06 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_000077 CDKN2A 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 Type 2 diabetes rs10811661 5.00E-06 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1
NM_004936 CDKN2B 17463249 http://www.ncbi.nlm.nih.gov/pubmed/17463249 Type 2 diabetes rs10811661 5.00E-06 Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes. NHGRI|-1