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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 7,073 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.134 higher; p = 3 × 10−11.
Where it sits Chromosome 8, band 8p23.1 — in an intron of TNKS.
What each result means
C/CPublished research associates this genotype with typical/baseline likelihood of Triacylglycerol 40:0(FA12:0) (Model 1) — 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 Triacylglycerol 40:0(FA12:0) (Model 1).
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Triacylglycerol 40:0(FA12:0) (Model 1) compared to the general population.
Nature communications · 2026 · PMID 42069741 · open access
Questions about rs10092751
What is rs10092751?
rs10092751 is a single position in the genome, in or near the TNKS gene. Published research associates it with triacylglycerol 40:0(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 rs10092751 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 rs10092751 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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