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X-21448 levels

USP40 · rs3796092

What the study found

Who was studied 8,809 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.174 higher (95% confidence interval 0.12-0.22); p = 3 × 10−12.

Where it sits Chromosome 2, band 2q37.1 — in an intron of USP40.

What each result means

A/A Two copies of the version the research linked to X-21448 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/C One copy of the version the research linked to X-21448 levels. That is a smaller link than two copies.
C/C No copy of the version the research linked to X-21448 levels. This is the starting point the study compared everyone against.
Source

Questions about rs3796092

What is rs3796092?

rs3796092 is a single position in the genome, in or near the USP40 gene. Published research associates it with x-21448 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs3796092 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 rs3796092 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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X-21448 levels (rs3796092). MyGeneLog™. https://www.mygenelog.com/variants/rs3796092

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