Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4788102
rs4788102
Entrez Id: 25970
Gene Symbol: SH2B1
SH2B1
CUI: C1956346
Disease:
Coronary Artery Disease
0.010 GeneticVariation BEFREE SNP rs4788102 (G/A) was not associated with CAD (overall allelic OR=1.06, 95% CI=0.93-1.21; p=0.37). 21907990 2011