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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 7,093 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.311 lower; p = 6 × 10−74.
Where it sits Chromosome 2, band 2q37.1 — in an intron of UGT1A9.
What each result means
C/CPublished research associates this genotype with typical/baseline likelihood of Diacylglycerol (14:1/18:1) (Model 2) — no copies of the reported risk allele.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Diacylglycerol (14:1/18:1) (Model 2).
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Diacylglycerol (14:1/18:1) (Model 2) compared to the general population.
Nature communications · 2026 · PMID 42069741 · open access
Questions about rs10179091
What is rs10179091?
rs10179091 is a single position in the genome, in or near the UGT1A3 gene. Published research associates it with diacylglycerol (14:1/18:1) (model 2). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10179091 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 rs10179091 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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