Sensitive

Coronary heart disease

PPAP2B · rs17114036

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What each result means

A/A 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)

A/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

Questions about rs17114036

What is rs17114036?

rs17114036 is a single position in the genome, in or near the PPAP2B gene. Published research associates it with coronary heart disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs17114036 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs17114036 come from?

GWAS Catalog, Nat Genet 2011, PMID:21378990. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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