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X-13684 levels

MPST · rs80236166

What the study found

Who was studied 8,809 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.212 lower (95% confidence interval 0.15-0.27); p = 1 × 10−11.

Where it sits Chromosome 22, band 22q12.3 — in an intron of MPST.

What each result means

A/A Two copies of the version the research linked to X-13684 levels. 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 X-13684 levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to X-13684 levels. This is the starting point the study compared everyone against.
Source

Questions about rs80236166

What is rs80236166?

rs80236166 is a single position in the genome, in or near the MPST gene. Published research associates it with x-13684 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs80236166 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 rs80236166 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-13684 levels (rs80236166). MyGeneLog™. https://www.mygenelog.com/variants/rs80236166

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