Standard

Triglycerides

near LINC01153 · rs11199812

Where this position leads

Condition: High Triglycerides

rs11199812 Condition: High Triglycerides High Triglycerides Condition rs11199812 rs11199812 near LINC011…

What the study found

Who was studied 343,992 European ancestry individuals, 111,667 East Asian ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0237 lower (95% confidence interval 0.016-0.032); p = 7 × 10−9.

Where it sits Chromosome 10, band 10q26.12 — between genes, 7.3 kb from LINC01153.

What each result means

A/A Two copies of the version the research linked to Triglycerides. 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 Triglycerides. That is a smaller link than two copies.
G/G No copy of the version the research linked to Triglycerides. This is the starting point the study compared everyone against.
Source

Questions about rs11199812

What is rs11199812?

rs11199812 is a single position in the genome, in or near the near LINC01153 gene. Published research associates it with triglycerides. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11199812 linked to?

On MyGeneLog this position is linked to High Triglycerides. The research behind each link, and its sources, are set out on that condition page.

Does having rs11199812 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 rs11199812 come from?

GWAS Catalog, Nature genetics 2021, PMID:34594039. 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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Triglycerides (rs11199812). MyGeneLog™. https://www.mygenelog.com/variants/rs11199812

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