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Total cholesterol levels

PPARG · rs75262919

What the study found

Who was studied 342,508 European ancestry individuals, 6,014 African ancestry individuals, 7,336 South Asian ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0324 lower (95% confidence interval 0.024-0.041); p = 7 × 10−14.

Where it sits Chromosome 3, band 3p25.2 — in an intron of PPARG.

What each result means

C/C No copy of the version the research linked to Total cholesterol levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Total cholesterol levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Total cholesterol levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs75262919

What is rs75262919?

rs75262919 is a single position in the genome, in or near the PPARG gene. Published research associates it with total cholesterol levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs75262919 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 rs75262919 come from?

GWAS Catalog, Nature genetics 2021, PMID:33462484. 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.

Total cholesterol levels (rs75262919). MyGeneLog™. https://www.mygenelog.com/variants/rs75262919

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