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Total cholesterol levels (MTAG)

TM4SF5 · rs59999069

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 T allele shifted the measure 0.029 lower (95% confidence interval 0.02-0.038); p = 3 × 10−11.

Where it sits Chromosome 17, band 17p13.2 — in an intron of TM4SF5.

What each result means

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

Questions about rs59999069

What is rs59999069?

rs59999069 is a single position in the genome, in or near the TM4SF5 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 rs59999069 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 rs59999069 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) (rs59999069). MyGeneLog™. https://www.mygenelog.com/variants/rs59999069

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