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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 342,233 European ancestry individuals, 6,014 African ancestry individuals, 7,330 South Asian ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.0158 lower (95% confidence interval 0.011-0.021); p = 2 × 10−9.
Where it sits Chromosome 4, band 4q32.1 — between genes, 25 kb from LINC02272.
What each result means
A/ANo copy of the version the research linked to Triglyceride levels. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Triglyceride levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Triglyceride levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2021 · PMID 33462484 · open access
Questions about rs10012484
What is rs10012484?
rs10012484 is a single position in the genome, in or near the near LINC02272 gene. Published research associates it with triglyceride levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10012484 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 rs10012484 come from?
GWAS Catalog, Nature genetics 2021, PMID:33462484. 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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