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N-delta-acetylornithine levels

ACTG2 · rs13415017

What the study found

Who was studied 8,809 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.147 lower (95% confidence interval 0.11-0.18); p = 2 × 10−15.

Where it sits Chromosome 2, band 2p13.1 — in an intron of ACTG2.

What each result means

C/C Two copies of the version the research linked to N-delta-acetylornithine levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to N-delta-acetylornithine levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to N-delta-acetylornithine levels. This is the starting point the study compared everyone against.
Source

Questions about rs13415017

What is rs13415017?

rs13415017 is a single position in the genome, in or near the ACTG2 gene. Published research associates it with n-delta-acetylornithine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs13415017 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 rs13415017 come from?

GWAS Catalog, Metabolites 2022, PMID:35050183. 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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N-delta-acetylornithine levels (rs13415017). MyGeneLog™. https://www.mygenelog.com/variants/rs13415017

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