Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10168266
rs10168266
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
T 0.800 GeneticVariation GWASDB A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23. 24097066

2013

dbSNP: rs10168266
rs10168266
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. 23143596

2012

dbSNP: rs10168266
rs10168266
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 GeneticVariation GWASDB Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. 23273568

2013

dbSNP: rs10168266
rs10168266
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB Functional variants in NFKBIE and RTKN2 involved in activation of the NF-κB pathway are associated with rheumatoid arthritis in Japanese. 23028356

2012

dbSNP: rs10174238
rs10174238
Oligoarticular Juvenile Idiopathic Arthritis
0.800 GeneticVariation GWASDB Dense genotyping of immune-related disease regions identifies 14 new susceptibility loci for juvenile idiopathic arthritis. 23603761

2013

dbSNP: rs10181656
rs10181656
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.820 GeneticVariation GWASDB High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. 23143596

2012

dbSNP: rs10931481
rs10931481
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 GeneticVariation GWASDB Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. 21408207

2011

dbSNP: rs10931481
rs10931481
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368

2013

dbSNP: rs11889341
rs11889341
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
T 0.800 GeneticVariation GWASDB Genetics of rheumatoid arthritis contributes to biology and drug discovery. 24390342

2014

dbSNP: rs13426947
rs13426947
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.800 GeneticVariation GWASDB High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. 23143596

2012

dbSNP: rs1517352
rs1517352
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
C 0.800 GeneticVariation GWASDB Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. 23128233

2012

dbSNP: rs1517352
rs1517352
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368

2013

dbSNP: rs1517352
rs1517352
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 GeneticVariation GWASDB Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. 21408207

2011

dbSNP: rs16833239
rs16833239
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.700 GeneticVariation GWASDB Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. 23273568

2013

dbSNP: rs3024921
rs3024921
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.800 GeneticVariation GWASDB Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. 22961000

2012

dbSNP: rs3024921
rs3024921
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.800 GeneticVariation GWASDB Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants. 22936693

2012

dbSNP: rs3024921
rs3024921
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368

2013

dbSNP: rs3821236
rs3821236
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.810 GeneticVariation GWASDB Differential genetic associations for systemic lupus erythematosus based on anti-dsDNA autoantibody production. 21408207

2011

dbSNP: rs3821236
rs3821236
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.810 GeneticVariation GWASDB Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus. 19165918

2008

dbSNP: rs3821236
rs3821236
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.800 GeneticVariation GWASDB Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy. 21779181

2011

dbSNP: rs3821236
rs3821236
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
A 0.800 GeneticVariation GWASDB Genome-wide association study of systemic sclerosis identifies CD247 as a new susceptibility locus. 20383147

2010

dbSNP: rs3821236
rs3821236
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.700 GeneticVariation GWASDB Genetic variants in STAT4 and HLA-DQ genes confer risk of hepatitis B virus-related hepatocellular carcinoma. 23242368

2013

dbSNP: rs6715106
rs6715106
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.800 GeneticVariation GWASDB High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. 23143596

2012

dbSNP: rs6715106
rs6715106
CUI: C0007570
Disease: Celiac Disease
Celiac Disease
0.800 GeneticVariation GWASDB Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. 22057235

2011

dbSNP: rs7572482
rs7572482
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.800 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997

2012