Standard

Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test)

ZNF831 · rs73306888

Where this position leads

Condition: Blood Pressure

rs73306888 Condition: Blood Pressure Blood Pressure Condition rs73306888 rs73306888 ZNF831

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) compared to the general population. (GWAS Catalog, PLoS One 2018, PMID:29912962)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test). (GWAS Catalog, PLoS One 2018, PMID:29912962)
G/G Published research associates this genotype with typical/baseline likelihood of Diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test) — no copies of the reported risk allele. (GWAS Catalog, PLoS One 2018, PMID:29912962)

Source: GWAS Catalog, PLoS One 2018, PMID:29912962

Questions about rs73306888

What is rs73306888?

rs73306888 is a single position in the genome, in or near the ZNF831 gene. Published research associates it with diastolic blood pressure x alcohol consumption (light vs heavy) interaction (2df test). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs73306888 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.

Does having rs73306888 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 rs73306888 come from?

GWAS Catalog, PLoS One 2018, PMID:29912962. 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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