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Blood pressure

ATP2B1 · rs17249754

Where this position leads

Condition: Blood Pressure

rs17249754 Condition: Blood Pressure Blood Pressure Condition rs17249754 rs17249754 ATP2B1

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Blood pressure — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2011, PMID:21572416)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Blood pressure. (GWAS Catalog, Nat Genet 2011, PMID:21572416)
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Blood pressure compared to the general population. (GWAS Catalog, Nat Genet 2011, PMID:21572416)

Source: GWAS Catalog, Nat Genet 2011, PMID:21572416

What people read about alongside this

Alcohol and the flush1 Exercise and muscle1

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs17249754

What is rs17249754?

rs17249754 is a single position in the genome, in or near the ATP2B1 gene. Published research associates it with blood pressure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs17249754 linked to?

On MyGeneLog this position is linked to Blood Pressure. The research behind each link, and its sources, are set out on that condition page.

What do people read about alongside rs17249754?

Subjects that appear in the title or abstract of the same papers as this rsID include alcohol and the flush (1 papers), exercise and muscle (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs17249754 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 rs17249754 come from?

GWAS Catalog, Nat Genet 2011, PMID:21572416. 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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