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Triacylglycerol 36:0(FA12:0) (Model 2)

FOLH1 · rs202677

What the study found

Who was studied 6,570 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.313 lower; p = 5 × 10−58.

Where it sits Chromosome 11, band 11p11.12 — in an intron of FOLH1.

What each result means

A/A Two copies of the version the research linked to Triacylglycerol 36:0(FA12:0) (Model 2). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/G One copy of the version the research linked to Triacylglycerol 36:0(FA12:0) (Model 2). That is a smaller link than two copies.
G/G No copy of the version the research linked to Triacylglycerol 36:0(FA12:0) (Model 2). This is the starting point the study compared everyone against.
Source

Questions about rs202677

What is rs202677?

rs202677 is a single position in the genome, in or near the FOLH1 gene. Published research associates it with triacylglycerol 36:0(fa12:0) (model 2). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs202677 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 rs202677 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.

Quoting this page

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Triacylglycerol 36:0(FA12:0) (Model 2) (rs202677). MyGeneLog™. https://www.mygenelog.com/variants/rs202677

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