Standard

Triglycerides

ACTB · rs852392

Where this position leads

Condition: High Triglycerides

rs852392 Condition: High Triglycerides High Triglycerides Condition rs852392 rs852392 ACTB

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 0.0151 higher (95% confidence interval 0.0098-0.0204); p = 1 × 10−8.

Where it sits Chromosome 7, band 7p22.1 — inside ACTB.

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 rs852392

What is rs852392?

rs852392 is a single position in the genome, in or near the ACTB 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 rs852392 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 rs852392 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 rs852392 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 (rs852392). MyGeneLog™. https://www.mygenelog.com/variants/rs852392

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