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Pulse pressure

LINC02931 · rs2840674

What the study found

Who was studied 360,863 European ancestry individuals, 145,445 East Asian ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0126 lower (95% confidence interval 0.0087-0.0165); p = 3 × 10−10.

Where it sits Chromosome X, band Xq26.3 — in an intron of LINC02931.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Pulse pressure compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Pulse pressure.
G/G Published research associates this genotype with typical/baseline likelihood of Pulse pressure — no copies of the reported risk allele.
Source

Questions about rs2840674

What is rs2840674?

rs2840674 is a single position in the genome, in or near the LINC02931 gene. Published research associates it with pulse pressure. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs2840674 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 rs2840674 come from?

GWAS Catalog, Nature genetics 2021, PMID:34594039. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Pulse pressure (rs2840674). MyGeneLog™. https://www.mygenelog.com/variants/rs2840674

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