Sensitive

Coronary heart disease

PHACTR1 · rs12526453

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What each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Coronary heart disease compared to the general population. (GWAS Catalog, Nat Genet 2011, PMID:21378990)
C/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Coronary heart disease. (GWAS Catalog, Nat Genet 2011, PMID:21378990)
G/G Published research associates this genotype with typical/baseline likelihood of Coronary heart disease — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2011, PMID:21378990)

Source: GWAS Catalog, Nat Genet 2011, PMID:21378990

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