RS17465637 Unknown gene

Other Chr 1:222650187
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What This Variant Does
"rs17465637 is a SNP found to be associated with heart disease by the German MI (Myocardial infarctio..."
GWAS Studies (6)
Trait Risk Allele OR / Beta P-value Study
Coronary artery disease A β: 0.082 8E-31 PubMed
Heart attack C OR: 0.11 2E-12 PubMed
Coronary artery disease (confirmatory factor analysis Factor 16) 6E-12 PubMed
Myocardial infarction (early onset) C OR: 1.14 1E-9 PubMed
Coronary heart disease C OR: 1.14 1E-8 PubMed
Coronary heart disease C OR: 1.2 1E-6 PubMed
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