Source: GWASDB

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3763317
rs3763317
CUI: C0577608
Disease: C4 complement assay (procedure)
C4 complement assay (procedure)
C 0.800 GeneticVariation GWASDB Genome-wide association study for serum complement C3 and C4 levels in healthy Chinese subjects. 23028341

2012

dbSNP: rs9268508
rs9268508
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805

2012

dbSNP: rs9268507
rs9268507
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805

2012

dbSNP: rs9268506
rs9268506
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805

2012

dbSNP: rs9268504
rs9268504
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805

2012

dbSNP: rs9268503
rs9268503
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805

2012

dbSNP: rs9268502
rs9268502
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805

2012

dbSNP: rs9268501
rs9268501
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805

2012

dbSNP: rs3763316
rs3763316
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761

2011

dbSNP: rs3763316
rs3763316
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805

2012

dbSNP: rs3763314
rs3763314
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.700 GeneticVariation GWASDB Genome-wide association study of African and European Americans implicates multiple shared and ethnic specific loci in sarcoidosis susceptibility. 22952805

2012

dbSNP: rs3763313
rs3763313
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction
C 0.700 GeneticVariation GWASDB A genome-wide association meta-analysis of self-reported allergy identifies shared and allergy-specific susceptibility loci. 23817569

2013

dbSNP: rs3763313
rs3763313
CUI: C0019829
Disease: Hodgkin Disease
Hodgkin Disease
A 0.700 GeneticVariation GWASDB Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma. 24149102

2013

dbSNP: rs3763313
rs3763313
Diabetes Mellitus, Insulin-Dependent
0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007

dbSNP: rs3763313
rs3763313
CUI: C0024301
Disease: Lymphoma, Follicular
Lymphoma, Follicular
0.700 GeneticVariation GWASDB A meta-analysis of genome-wide association studies of follicular lymphoma. 23025665

2012

dbSNP: rs3763313
rs3763313
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.700 GeneticVariation GWASDB Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease. 18587394

2008

dbSNP: rs3817973
rs3817973
Diabetes Mellitus, Insulin-Dependent
0.700 GeneticVariation GWASDB A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene. 17632545

2007

dbSNP: rs3817973
rs3817973
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761

2011

dbSNP: rs3817973
rs3817973
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. 17804836

2007

dbSNP: rs3129953
rs3129953
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.700 GeneticVariation GWASDB A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. 21156761

2011

dbSNP: rs2076530
rs2076530
CUI: C0036202
Disease: Sarcoidosis
Sarcoidosis
0.900 GeneticVariation GWASDB Genome-wide association analysis reveals 12q13.3-q14.1 as new risk locus for sarcoidosis. 22936702

2013

dbSNP: rs3817963
rs3817963
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
Adenocarcinoma of lung (disorder)
G 0.810 GeneticVariation GWASDB A genome-wide association study identifies two new susceptibility loci for lung adenocarcinoma in the Japanese population. 22797724

2012

dbSNP: rs10947262
rs10947262
CUI: C0409959
Disease: Osteoarthritis, Knee
Osteoarthritis, Knee
T 0.810 GeneticVariation GWASDB New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study. 20305777

2010

dbSNP: rs3817963
rs3817963
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis
0.800 GeneticVariation GWASDB Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. 23472185

2013

dbSNP: rs3806156
rs3806156
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.800 GeneticVariation GWASDB Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. 22561518

2012