RS3782889 Unknown gene

Other Chr 12:110912851
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What This Variant Does
"A genome-wide association study of a coronary artery disease risk variant"
GWAS Studies (3)
Trait Risk Allele OR / Beta P-value Study
Coronary heart disease C OR: 1.26 4E-14 PubMed
Metabolic syndrome (multivariate analysis) — — 1E-9 PubMed
Hypertension G OR: 0.84 2E-8 PubMed
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