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Serum potassium levels

KLHL3 · rs17797119

What the study found

Who was studied 38,000 South Asian ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.051 lower (95% confidence interval 0.035-0.067); p = 2 × 10−10.

Where it sits Chromosome 5, band 5q31.2 — in an intron of KLHL3.

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Serum potassium levels — 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 Serum potassium levels.
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Serum potassium levels compared to the general population.
Source

Questions about rs17797119

What is rs17797119?

rs17797119 is a single position in the genome, in or near the KLHL3 gene. Published research associates it with serum potassium levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs17797119 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 rs17797119 come from?

GWAS Catalog, Nature communications 2024, PMID:39414775. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Serum potassium levels (rs17797119). MyGeneLog™. https://www.mygenelog.com/variants/rs17797119

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