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Volume of heart

near KRT18P16 · rs984169

What the study found

Who was studied 35,492 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0465 lower (95% confidence interval 0.032-0.061); p = 2 × 10−10.

Where it sits Chromosome 5, band 5q23.2 — between genes, 68 kb from KRT18P16.

What each result means

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

Questions about rs984169

What is rs984169?

rs984169 is a single position in the genome, in or near the near KRT18P16 gene. Published research associates it with volume of heart. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs984169 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 rs984169 come from?

GWAS Catalog, Communications medicine 2026, PMID:41629584. 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.

Volume of heart (rs984169). MyGeneLog™. https://www.mygenelog.com/variants/rs984169

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