Standard

Triacylglycerol 36:0(FA12:0) (Model 1)

near FADS2B · rs1792498

What the study found

Who was studied 6,724 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.146 lower; p = 5 × 10−14.

Where it sits Chromosome 11, band 11q12.1 — between genes, 0.9 kb from FADS2B.

What each result means

C/C No 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.
C/T One copy of the version the research linked to Triacylglycerol 36:0(FA12:0) (Model 1). That is a smaller link than two copies.
T/T Two 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.
Source

Questions about rs1792498

What is rs1792498?

rs1792498 is a single position in the genome, in or near the near 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 rs1792498 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 rs1792498 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 1) (rs1792498). MyGeneLog™. https://www.mygenelog.com/variants/rs1792498

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