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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 22,000 Pakistani and Bangladeshi ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.08 lower (95% confidence interval 0.06-0.1); p = 1 × 10−8.
How common The C allele had a frequency of about 28% in the people studied.
Where it sits Chromosome 11, band 11q23.3 — in an intron of SIK3.
What each result means
A/ANo copy of the version the research linked to Triacylglyceride levels. This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Triacylglyceride levels. That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Triacylglyceride levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2022 · PMID 35945198 · open access
Questions about rs10892063
What is rs10892063?
rs10892063 is a single position in the genome, in or near the SIK3 gene. Published research associates it with triacylglyceride levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10892063 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 rs10892063 come from?
GWAS Catalog, Nature communications 2022, PMID:35945198. 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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