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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 A allele shifted the measure 0.253 higher; p = 1 × 10−13.
Where it sits Chromosome 11, band 11q12.1 — between genes, 2 kb from LPXN.
What each result means
A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Triacylglycerol 36:0(FA12:0) (Model 1) compared to the general population.
A/GPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Triacylglycerol 36:0(FA12:0) (Model 1).
G/GPublished research associates this genotype with typical/baseline likelihood of Triacylglycerol 36:0(FA12:0) (Model 1) — no copies of the reported risk allele.
Nature communications · 2026 · PMID 42069741 · open access
Questions about rs71486420
What is rs71486420?
rs71486420 is a single position in the genome, in or near the near LPXN 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 rs71486420 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 rs71486420 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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