Source: GWASCAT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs8099917
rs8099917
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
G 0.900 GeneticVariation GWASCAT IL28B is associated with response to chronic hepatitis C interferon-alpha and ribavirin therapy. 19749758

2009

dbSNP: rs8099917
rs8099917
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
G 0.900 GeneticVariation GWASCAT Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study. 20060832

2010

dbSNP: rs8099917
rs8099917
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
G 0.900 GeneticVariation GWASCAT IL-28B predicts response to chronic hepatitis C therapy--fine-mapping and replication study in Asian populations. 21228123

2011

dbSNP: rs8099917
rs8099917
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
G 0.900 GeneticVariation GWASCAT Genome-wide association of IL28B with response to pegylated interferon-alpha and ribavirin therapy for chronic hepatitis C. 19749757

2009

dbSNP: rs744373
rs744373
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.900 GeneticVariation GWASCAT Meta-analysis for genome-wide association study identifies multiple variants at the BIN1 locus associated with late-onset Alzheimer's disease. 21390209

2011

dbSNP: rs744373
rs744373
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.900 GeneticVariation GWASCAT Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. 21460840

2011

dbSNP: rs744373
rs744373
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.900 GeneticVariation GWASCAT The membrane-spanning 4-domains, subfamily A (MS4A) gene cluster contains a common variant associated with Alzheimer's disease. 21627779

2011

dbSNP: rs6920220
rs6920220
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.900 GeneticVariation GWASCAT Common variants at CD40 and other loci confer risk of rheumatoid arthritis. 18794853

2008

dbSNP: rs6920220
rs6920220
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.900 GeneticVariation GWASCAT Two independent alleles at 6q23 associated with risk of rheumatoid arthritis. 17982456

2007

dbSNP: rs6920220
rs6920220
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.900 GeneticVariation GWASCAT Novel rheumatoid arthritis susceptibility locus at 22q12 identified in an extended UK genome-wide association study. 24449572

2014

dbSNP: rs6920220
rs6920220
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
A 0.900 GeneticVariation GWASCAT High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. 23143596

2012

dbSNP: rs6920220
rs6920220
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
A 0.900 GeneticVariation GWASCAT Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. 20453842

2010

dbSNP: rs6920220
rs6920220
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
A 0.900 GeneticVariation GWASCAT High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci. 24532676

2015

dbSNP: rs5015480
rs5015480
Diabetes Mellitus, Non-Insulin-Dependent
C 0.900 GeneticVariation GWASCAT Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. 20581827

2010

dbSNP: rs5015480
rs5015480
Diabetes Mellitus, Non-Insulin-Dependent
C 0.900 GeneticVariation GWASCAT Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes. 18372903

2008

dbSNP: rs5015480
rs5015480
Diabetes Mellitus, Non-Insulin-Dependent
C 0.900 GeneticVariation GWASCAT Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases. 22693455

2012

dbSNP: rs4444235
rs4444235
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.900 GeneticVariation GWASCAT Genome-wide association study of colorectal cancer identifies six new susceptibility loci. 26151821

2015

dbSNP: rs4444235
rs4444235
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.900 GeneticVariation GWASCAT We identified four previously unreported CRC risk loci at 14q22.2 (rs4444235, BMP4; P = 8.1 x 10(-10)), 16q22.1 (rs9929218, CDH1; P = 1.2 x 10(-8)), 19q13.1 (rs10411210, RHPN2; P = 4.6 x 10(-9)) and 20p12.3 (rs961253; P = 2.0 x 10(-10)). 19011631

2008

dbSNP: rs4444235
rs4444235
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
C 0.900 GeneticVariation GWASCAT Novel Common Genetic Susceptibility Loci for Colorectal Cancer. 29917119

2019

dbSNP: rs3851179
rs3851179
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.900 GeneticVariation GWASCAT These associations were replicated in stage 2 (2,023 cases and 2,340 controls), producing compelling evidence for association with Alzheimer's disease in the combined dataset (rs11136000, P = 8.5 x 10(-10), odds ratio = 0.86; rs3851179, P = 1.3 x 10(-9), odds ratio = 0.86). 19734902

2009

dbSNP: rs35705950
rs35705950
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
T 0.900 GeneticVariation GWASCAT Genetic variants associated with idiopathic pulmonary fibrosis susceptibility and mortality: a genome-wide association study. 24429156

2013

dbSNP: rs35705950
rs35705950
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
T 0.900 GeneticVariation GWASCAT Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. 29066090

2017

dbSNP: rs2943641
rs2943641
Diabetes Mellitus, Non-Insulin-Dependent
C 0.900 GeneticVariation GWASCAT Unlike previously reported T2D risk loci, which predominantly associate with impaired beta cell function, the C allele of rs2943641 was associated with insulin resistance and hyperinsulinemia in 14,358 French, Danish and Finnish participants from population-based cohorts; this allele was also associated with reduced basal levels of IRS1 protein and decreased insulin induction of IRS1-associated phosphatidylinositol-3-OH kinase activity in human skeletal muscle biopsies. 19734900

2009

dbSNP: rs2200733
rs2200733
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
T 0.900 GeneticVariation GWASCAT Variants conferring risk of atrial fibrillation on chromosome 4q25. 17603472

2007

dbSNP: rs2200733
rs2200733
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
0.900 GeneticVariation GWASCAT A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. 19597491

2009