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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 11,296 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0864 higher (95% confidence interval 0.058-0.115); p = 4 × 10−9.
How common The C allele had a frequency of about 70% in the people studied.
Where it sits Chromosome 11, band 11q12.1 — in an intron of MIR130AHG.
What each result means
C/CTwo copies of the version the research linked to Serum lipopolysaccharide activity. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Serum lipopolysaccharide activity. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Serum lipopolysaccharide activity. This is the starting point the study compared everyone against.
Journal of the American Heart Association · 2021 · PMID 34668383 · open access
Questions about rs2081361
What is rs2081361?
rs2081361 is a single position in the genome, in or near the MIR130AHG gene. Published research associates it with serum lipopolysaccharide activity. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs2081361 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 rs2081361 come from?
GWAS Catalog, Journal of the American Heart Association 2021, PMID:34668383. 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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