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Urinary 3-aminoisobutyrate to urinary creatinine ratio

TTC23L · rs138425947

What the study found

Who was studied 6,347 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.52 lower (95% confidence interval 0.38-0.66); p = 2 × 10−14.

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

Where it sits Chromosome 5, band 5p13.2 — in an intron of TTC23L.

What each result means

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

Questions about rs138425947

What is rs138425947?

rs138425947 is a single position in the genome, in or near the TTC23L gene. Published research associates it with urinary 3-aminoisobutyrate 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 rs138425947 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 rs138425947 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-aminoisobutyrate to urinary creatinine ratio (rs138425947). MyGeneLog™. https://www.mygenelog.com/variants/rs138425947

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