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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 6,724 European ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.498 lower; p = 2 × 10−13.
Where it sits Chromosome 11, band 11q12.1 — in an intron of FADS2B.
What each result means
A/ATwo copies of the version the research linked to Triacylglycerol 36:0(FA12:0) (Model 1). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Triacylglycerol 36:0(FA12:0) (Model 1). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Triacylglycerol 36:0(FA12:0) (Model 1). This is the starting point the study compared everyone against.
Nature communications · 2026 · PMID 42069741 · open access
Questions about rs111635595
What is rs111635595?
rs111635595 is a single position in the genome, in or near the FADS2B gene. Published research associates it with triacylglycerol 36:0(fa12:0) (model 1). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs111635595 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 rs111635595 come from?
GWAS Catalog, Nature communications 2026, PMID:42069741. 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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