Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2230926
rs2230926
TNFAIP3
0.030 GeneticVariation BEFREE TNFAIP3 F127C Coding Variation in Greek Primary Sjogren's Syndrome Patients. 30662920

2018
dbSNP: rs2230926
rs2230926
TNFAIP3
0.030 GeneticVariation BEFREE In both cohorts, the rs2230926 missense polymorphism was not associated with pSS. 26338037

2016
dbSNP: rs2230926
rs2230926
TNFAIP3
0.030 GeneticVariation BEFREE The rs2230926 exonic variant was associated with an increased risk for pSS complicated by lymphoma (odds ratio, 3.36 [95% confidence interval, 1.34-8.42], and odds ratio, 3.26 [95% confidence interval, 1.31-8.12], vs controls and pSS patients without lymphoma, respectively; P = .011). 24159176

2013