Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1004819
rs1004819
0.010 GeneticVariation BEFREE In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods. 19522770

2009

dbSNP: rs10168266
rs10168266
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
T 0.800 GeneticVariation GWASCAT A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23. 24097066

2013

dbSNP: rs10489629
rs10489629
0.010 GeneticVariation BEFREE In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods. 19522770

2009

dbSNP: rs10553577
rs10553577
T 0.700 GeneticVariation GWASCAT Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome. 24097067

2013

dbSNP: rs10774671
rs10774671
0.020 GeneticVariation BEFREE The SS risk allele of rs10774671 has been shown by others to be associated with reduced OAS1 enzymatic activity and ability to clear viral infections, as well as reduced responsiveness to IFN treatment. 28640813

2017

dbSNP: rs10774671
rs10774671
0.020 GeneticVariation BEFREE Our data demonstrated that the functional variant, rs10774671, is associated with HBV infection and anti-SSA antibody-positive SS. 29242559

2017

dbSNP: rs1085308048
rs1085308048
0.010 GeneticVariation BEFREE This report describes a novel PTEN mutation (L139X) in a patient with Cowden disease and Sjögren's syndrome. 10193515

1998

dbSNP: rs10889677
rs10889677
0.010 GeneticVariation BEFREE In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods. 19522770

2009

dbSNP: rs11048434
rs11048434
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017

dbSNP: rs11209026
rs11209026
0.010 GeneticVariation BEFREE In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods. 19522770

2009

dbSNP: rs11209032
rs11209032
0.010 GeneticVariation BEFREE In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods. 19522770

2009

dbSNP: rs1143634
rs1143634
0.010 GeneticVariation BEFREE It is suggested that rs1143634 of IL1B and rs8192284 of IL6R act as susceptibility variations in Korean non-Sjogren dry eye patients. 22128229

2011

dbSNP: rs115575857
rs115575857
G 0.700 GeneticVariation GWASCAT Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome. 24097067

2013

dbSNP: rs116855232
rs116855232
0.010 GeneticVariation BEFREE In this report, we first provide detailed clinical and laboratory characteristics of AZA-induced leukopenia in a patient with SS with a mutant NUDT15 R139C genotype (TT allele) and normal TPMT activity. 29702976

2018

dbSNP: rs117026326
rs117026326
T 0.800 GeneticVariation GWASCAT A genome-wide association study in Han Chinese identifies a susceptibility locus for primary Sjögren's syndrome at 7q11.23. 24097066

2013

dbSNP: rs117026326
rs117026326
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: rs117026326
rs117026326
T 0.800 GeneticVariation GWASCAT Identification of susceptibility gene associated with female primary Sjögren's syndrome in Han Chinese by genome-wide association study. 27503288

2016

dbSNP: rs11805303
rs11805303
0.010 GeneticVariation BEFREE In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods. 19522770

2009

dbSNP: rs11889341
rs11889341
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017

dbSNP: rs1507153
rs1507153
A 0.700 GeneticVariation GWASCAT Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome. 24097067

2013

dbSNP: rs17074492
rs17074492
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017

dbSNP: rs17339836
rs17339836
T 0.700 GeneticVariation GWASCAT Variants at multiple loci implicated in both innate and adaptive immune responses are associated with Sjögren's syndrome. 24097067

2013

dbSNP: rs1957173
rs1957173
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017

dbSNP: rs2201841
rs2201841
0.010 GeneticVariation BEFREE In our study, we genotyped groups of patients with AS (n = 206), SS (n = 156) and healthy controls (n = 235) for rs11805303, rs10889677, rs1004819, rs2201841, rs11209032, rs11209026, rs10489629, rs7517847 and rs7530511 variants using PCR-RFLP methods. 19522770

2009