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Total cholesterol levels (MTAG)

TTC39B · rs12348997

What the study found

Who was studied 125,000 African ancestry individuals (MTAG boosted by high-density lipoprotein and triglyceride samples).

The effect Each copy of the A allele shifted the measure 0.024 lower (95% confidence interval 0.017-0.031); p = 2 × 10−11.

Where it sits Chromosome 9, band 9p22.3 — in an intron of TTC39B.

What each result means

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

Questions about rs12348997

What is rs12348997?

rs12348997 is a single position in the genome, in or near the TTC39B gene. Published research associates it with total cholesterol levels (mtag). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs12348997 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 rs12348997 come from?

GWAS Catalog, Nature communications 2023, PMID:37669986. 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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Total cholesterol levels (MTAG) (rs12348997). MyGeneLog™. https://www.mygenelog.com/variants/rs12348997

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