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 the study found
Who was studied 927 Saudi Arabian ancestry cases, 3,159 Saudi Arabian ancestry controls; replicated in 317 Saudi Arabian ancestry cases, 1,098 Saudi Arabian ancestry controls.
The effect Each copy of the C allele carried 1.30 times the odds of Hypertriglyceridemia; p = 1 × 10−6.
Where it sits Chromosome 8, band 8q24.13 — in an intron of TRIB1AL.
What people read about alongside this
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
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.
Subjects that appear in the title or abstract of the same papers as this rsID include heart and circulation (3 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
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.
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.
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Hypertriglyceridemia (rs6982502). MyGeneLog™. https://www.mygenelog.com/variants/rs6982502