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Triglyceride to HDL cholesterol ratio

near AMBRA1 · rs147244995

What the study found

Who was studied 402,398 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0952 higher (95% confidence interval 0.074-0.117); p = 2 × 10−12.

How common The C allele had a frequency of about 99% in the people studied.

Where it sits Chromosome 11, band 11p11.2 — between genes, 0.3 kb from AMBRA1.

What each result means

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

Questions about rs147244995

What is rs147244995?

rs147244995 is a single position in the genome, in or near the near AMBRA1 gene. Published research associates it with triglyceride to hdl cholesterol ratio. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs147244995 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 rs147244995 come from?

GWAS Catalog, Nature genetics 2024, PMID:38200128. 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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Triglyceride to HDL cholesterol ratio (rs147244995). MyGeneLog™. https://www.mygenelog.com/variants/rs147244995

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