Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs266089
rs266089
Entrez Id: 6387
Gene Symbol: CXCL12
CXCL12
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE In the allele model, rs1065297, rs266089 and rs10793538 in <i>CXCL12</i> gene associated with the risk of CAD. 28903360 2017