Standard

Hypertriglyceridemia

TRIB1 · rs6982502

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 each result means

C/C Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Hypertriglyceridemia compared to the general population.

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Hypertriglyceridemia.

T/T Published research associates this genotype with typical/baseline likelihood of Hypertriglyceridemia — no copies of the reported risk allele.

Source

A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia

Ram R, Wakil SM, Muiya NP, Andres E, Mazhar N, Hagos S, Alshahid M, Meyer BF, Morahan G, Dzimiri N

Clinical genetics · 2017 · PMID 27599772

Questions about rs6982502

What is rs6982502?

rs6982502 is a single position in the genome, in or near the TRIB1 gene. Published research associates it with hypertriglyceridemia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs6982502 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 rs6982502 come from?

GWAS Catalog, Clin Genet 2016, PMID:27599772. 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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