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Free cholesterol to total lipids ratio in medium LDL

BNC2 · rs10810645

What the study found

Who was studied 4,435 East Asian ancestry individuals, 11,340 South Asian ancestry individuals, 120,241 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0266 lower (95% confidence interval 0.018-0.035); p = 3 × 10−10.

How common The A allele had a frequency of about 40% in the people studied.

Where it sits Chromosome 9, band 9p22.2 — in an intron of BNC2.

What each result means

A/A Two copies of the version the research linked to Free cholesterol to total lipids ratio in medium LDL. 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 Free cholesterol to total lipids ratio in medium LDL. That is a smaller link than two copies.
G/G No copy of the version the research linked to Free cholesterol to total lipids ratio in medium LDL. This is the starting point the study compared everyone against.
Source

Questions about rs10810645

What is rs10810645?

rs10810645 is a single position in the genome, in or near the BNC2 gene. Published research associates it with free cholesterol to total lipids ratio in medium ldl. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10810645 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 rs10810645 come from?

GWAS Catalog, Nature 2024, PMID:38448586. 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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Free cholesterol to total lipids ratio in medium LDL (rs10810645). MyGeneLog™. https://www.mygenelog.com/variants/rs10810645

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