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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 239,268 European ancestry individuals.
The effect
The reported allele is A; the catalogue records no effect size
; p = 1 × 10−111.
Where it sits Chromosome 11, band 11q12.2 — a missense change in TMEM258.
What each result means
A/ATwo copies of the version the research linked to Docosahexaenoic acid levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Docosahexaenoic acid levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Docosahexaenoic acid levels. This is the starting point the study compared everyone against.
rs117110139 is a single position in the genome, in or near the TMEM258 gene. Published research associates it with docosahexaenoic acid levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs117110139 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 rs117110139 come from?
GWAS Catalog, HGG advances 2025, PMID:40545721. 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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