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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 6,724 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.664 lower; p = 1 × 10−11.
Where it sits Chromosome 11, band 11p11.12 — between genes, 12.7 kb from OR4C12.
What each result means
G/GNo copy of the version the research linked to Triacylglycerol 36:0(FA12:0) (Model 1). This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to Triacylglycerol 36:0(FA12:0) (Model 1). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Triacylglycerol 36:0(FA12:0) (Model 1). That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2026 · PMID 42069741 · open access
Questions about rs183959498
What is rs183959498?
rs183959498 is a single position in the genome, in or near the near OR4C12 gene. Published research associates it with triacylglycerol 36:0(fa12:0) (model 1). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs183959498 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 rs183959498 come from?
GWAS Catalog, Nature communications 2026, PMID:42069741. 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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