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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 4,642 European ancestry women.
The effect
Each copy of the T allele shifted the measure 0.187 higher (95% confidence interval 0.13-0.24); p = 1 × 10−10.
Where it sits Chromosome 16, band 16p13.11 — in an intron of BMERB1.
What each result means
C/CNo copy of the version the research linked to Sterol ester (27:1/20:3) levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Sterol ester (27:1/20:3) levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Sterol ester (27:1/20:3) levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Journal of the American Heart Association · 2022 · PMID 36193934 · open access
Questions about rs117975403
What is rs117975403?
rs117975403 is a single position in the genome, in or near the BMERB1 gene. Published research associates it with sterol ester (27:1/20:3) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs117975403 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 rs117975403 come from?
GWAS Catalog, Journal of the American Heart Association 2022, PMID:36193934. 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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