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Triglyceride levels

near TRIB1 · rs2980888

What the study found

Who was studied 6,949 Korean ancestry individuals; replicated in 6,000 Korean ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0506 higher; p = 5 × 10−8.

How common The T allele had a frequency of about 28% in the people studied.

Where it sits Chromosome 8, band 8q24.13 — in an intron of TRIB1AL.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Triglyceride levels — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Triglyceride levels.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Triglyceride levels compared to the general population.
Source

Questions about rs2980888

What is rs2980888?

rs2980888 is a single position in the genome, in or near the near TRIB1 gene. Published research associates it with triglyceride levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs2980888 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 rs2980888 come from?

GWAS Catalog, Sci Rep 2019, PMID:30718733. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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.

Triglyceride levels (rs2980888). MyGeneLog™. https://www.mygenelog.com/variants/rs2980888

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