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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 4,642 European ancestry women.
The effect
Each copy of the C allele shifted the measure 0.941 higher (95% confidence interval 0.73-1.16); p = 2 × 10−17.
Where it sits Chromosome 15, band 15q22.2 — in a non-coding transcript of MYO1E.
What each result means
C/CTwo copies of the version the research linked to Phosphatidylethanolamine (16:0_20:4) levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Phosphatidylethanolamine (16:0_20:4) levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Phosphatidylethanolamine (16:0_20:4) levels. This is the starting point the study compared everyone against.
Journal of the American Heart Association · 2022 · PMID 36193934 · open access
Questions about rs112884731
What is rs112884731?
rs112884731 is a single position in the genome, in or near the MYO1E gene. Published research associates it with phosphatidylethanolamine (16:0_20:4) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs112884731 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 rs112884731 come from?
GWAS Catalog, Journal of the American Heart Association 2022, PMID:36193934. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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