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Parent Gene: C10ORF32-ASMT, CYP17A1
Importance: 4
Minor Allele: None = None
Major Allele: T = None
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Risk Allele: T

Disease/Trait: Coronary Artery Disease

The T allele of rs11191416 is reported to be associated with Coronary Artery Disease(R). Your genotype was not identified for this SNP so we are unable to comment on your association with Coronary artery disease.

Reported risk allele frequency: 87.25%
Reported genes: C10ORF32-ASMT , CYP17A1
Odds ratio: 1.08
Risk Allele: T (P=5.00*10-9)
Context: intron_variant
Study title: A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease. (R)
Initial sample size: 42,096 European ancestry cases, 361 African American cases, 758 Hispanic American cases, 12,658 South Asian ancestry cases, 1,802 Lebanese ancestry cases, 3,614 East Asian ancestry cases, 99,121 European ancestry controls, 2,778 African American controls, 3,337 Hispanic American controls, 12,899 South Asian ancestry controls, 466 Lebanese ancestry controls, 7,709 East Asian ancestry controls
Replication sample size:
Journal: Nat Genet (R)
Year published: Sept. 7, 2015
Strength of evidence: Strong