A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Blood pressure (anthropometric measures interaction) compared to the general population.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Blood pressure (anthropometric measures interaction).
G/GPublished research associates this genotype with typical/baseline likelihood of Blood pressure (anthropometric measures interaction) — no copies of the reported risk allele.
BMC medical genetics · 2014 · PMID 24903457 · open access
Questions about rs13390641
What is rs13390641?
rs13390641 is a single position in the genome, in or near the TMEM182 gene. Published research associates it with blood pressure (anthropometric measures interaction). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs13390641 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 rs13390641 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 rs13390641 come from?
GWAS Catalog, BMC Med Genet 2014, PMID:24903457. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.