Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1234313
rs1234313
Entrez Id: 7292
Gene Symbol: TNFSF4
TNFSF4
CUI: C0151449
Disease:
Primary Sjögren's syndrome
0.010 GeneticVariation BEFREE In TNFSF4, T allele and TT genotype of rs2205960, and G allele of rs1234313, were associated with pSS (p<0.05); T allele of rs2205960 was correlated with PBC (p<0.05) as a risk factor. 23622253 2013