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Urinary 3-hydroxyisovalerate to urinary creatinine ratio

ACSM2B · rs7499358

What the study found

Who was studied 8,007 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.62 lower (95% confidence interval 0.5-0.74); p = 8 × 10−22.

How common The A allele had a frequency of about 98% in the people studied.

Where it sits Chromosome 16, band 16p12.3 — in an intron of ACSM2B.

What each result means

A/A Two copies of the version the research linked to Urinary 3-hydroxyisovalerate to urinary creatinine ratio. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/T One copy of the version the research linked to Urinary 3-hydroxyisovalerate to urinary creatinine ratio. That is a smaller link than two copies.
T/T No copy of the version the research linked to Urinary 3-hydroxyisovalerate to urinary creatinine ratio. This is the starting point the study compared everyone against.
Source

Questions about rs7499358

What is rs7499358?

rs7499358 is a single position in the genome, in or near the ACSM2B gene. Published research associates it with urinary 3-hydroxyisovalerate to urinary creatinine ratio. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs7499358 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 rs7499358 come from?

GWAS Catalog, Nature communications 2025, PMID:39746953. 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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Urinary 3-hydroxyisovalerate to urinary creatinine ratio (rs7499358). MyGeneLog™. https://www.mygenelog.com/variants/rs7499358

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