TNFSF13B, TNF superfamily member 13b, 10673

N. diseases: 282; N. variants: 13
Disease: Primary Sjögren's syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12583006
rs12583006
Entrez Id: 10673
Gene Symbol: TNFSF13B
TNFSF13B
CUI: C0151449
Disease:
Primary Sjögren's syndrome 		0.010 GeneticVariation BEFREE The low risk pSS group exhibited higher frequency of the minor A allele and AA genotype of the rs12583006 variant compared to HC. 23845207 2014