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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 G allele shifted the measure 0.14 higher (95% confidence interval 0.095-0.184); p = 6 × 10−10.
Where it sits Chromosome 11, band 11q12.2 — in an intron of FADS2.
What each result means
C/CNo copy of the version the research linked to Triacylglycerol (54:3) levels. This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Triacylglycerol (54:3) levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Triacylglycerol (54:3) 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 rs174612
What is rs174612?
rs174612 is a single position in the genome, in or near the FADS2 gene. Published research associates it with triacylglycerol (54:3) levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs174612 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 rs174612 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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