Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11889341
rs11889341
CUI: C1527336
Disease: Sjogren's Syndrome
Sjogren's Syndrome
0.700 GeneticVariation GWASCAT Genome-Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry. 28076899

2017