Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11048434
rs11048434
KLRG1
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017
dbSNP: rs11889341
rs11889341
STAT4
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017
dbSNP: rs17074492
rs17074492
LOC105370283
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017
dbSNP: rs1957173
rs1957173 		0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017
dbSNP: rs3823536
rs3823536
IRF5
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017
dbSNP: rs7341475
rs7341475
RELN
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017
dbSNP: rs7574865
rs7574865
STAT4
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017
dbSNP: rs7999279
rs7999279 		0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017
dbSNP: rs9271573
rs9271573 		0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017
dbSNP: rs9277554
rs9277554
HLA-DPB1
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017
dbSNP: rs9938751
rs9938751
SHISA9
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017
dbSNP: rs10774671
rs10774671
OAS1
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
OAS1
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: rs2230926
rs2230926
TNFAIP3
0.020 GeneticVariation BEFREE Increased prevalence of the rs2230926 mutant variant was detected in both SS-lymphoma and SS-nonlymphoma subgroups compared to HC (8.8% vs. 7.6% vs. 3.6%, <i>p</i> values: 0.04 and 0.03, respectively) in association with higher IgM, LDH serum levels, and PB <i>Bcl-XL</i> transcripts but lower leucocyte and neutrophil counts. 30662920

2018
dbSNP: rs2230926
rs2230926
TNFAIP3
0.020 GeneticVariation BEFREE Genotyping of the most common coding polymorphism, rs2230926, in the MADGC collection and additional control individuals revealed a significant association with Sjögren's syndrome (OR=3.38, P=0.038), Crohn's disease (OR=2.25, P=0.041), psoriasis (OR=0.037, P=0.036) and RA (OR=1.9, P=0.025). 21326317

2011
dbSNP: rs1004819
rs1004819
IL23R ; C1orf141
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: rs10489629
rs10489629
IL23R ; C1orf141
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: rs1085308048
rs1085308048
PTEN
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
IL23R
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: rs11209026
rs11209026
IL23R
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
IL1B
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: rs116855232
rs116855232
NUDT15
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: rs11805303
rs11805303
IL23R ; C1orf141
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: rs2201841
rs2201841
IL23R ; C1orf141
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