TNFSF4, TNF superfamily member 4, 7292

N. diseases: 129; N. variants: 32
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3850641
rs3850641
Entrez Id: 7292
Gene Symbol: TNFSF4
TNFSF4
CUI: C0038454
Disease:
Cerebrovascular accident
0.010 GeneticVariation BEFREE Genotypic analysis demonstrated that there was no significant association between the risk of CHD and stroke and rs3850641 [homozygous comparison (GG vs. AA): OR=1.05, 95% CI=0.74-1.50; heterozygous comparison (GA vs. AA): OR=1.00, 95% CI=0.88-1.13; recessive model (GG vs. GA+AA): OR=1.04, 95% CI=0.76-1.43; dominant model (GG+GA vs. AA): OR=1.01, 95% CI=0.88-1.17]. 29424751 2018