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Cholesteryl Esters to Total Lipids in Large LDL percentage

near HPN · rs11671010

Where this position leads

Condition: Cholesterol (LDL, HDL and Total)

rs11671010 Condition: Cholesterol (LDL, HDL and Total) Cholesterol (LDL, HDL and Total) Condition rs11671010 rs11671010 near HPN

Strength of the evidence

3 / 4

Its strongest genetic-study result is p = 10−136, with 11 associations in the GWAS Catalog.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What the study found

Who was studied 434,646 British ancestry individuals, 8,796 British Central/South Asian individuals, 6,573 British African individuals.

The effect Each copy of the C allele shifted the measure 0.02 % lower (95% confidence interval 0.02-0.02); p = 1 × 10−17.

Where it sits Chromosome 19, band 19q13.11 — in an intron of HPN-AS1.

What each result means

C/C Two copies of the version the research linked to Cholesteryl Esters to Total Lipids in Large LDL percentage. 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 Cholesteryl Esters to Total Lipids in Large LDL percentage. That is a smaller link than two copies.
T/T No copy of the version the research linked to Cholesteryl Esters to Total Lipids in Large LDL percentage. This is the starting point the study compared everyone against.
Source

Questions about rs11671010

What is rs11671010?

rs11671010 is a single position in the genome, in or near the near HPN gene. Published research associates it with cholesteryl esters to total lipids in large ldl percentage. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11671010 linked to?

On MyGeneLog this position is linked to Cholesterol (LDL, HDL and Total). The research behind each link, and its sources, are set out on that condition page.

Does having rs11671010 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 rs11671010 come from?

GWAS Catalog, Nature genetics 2025, PMID:41044249. 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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Cholesteryl Esters to Total Lipids in Large LDL percentage (rs11671010). MyGeneLog™. https://www.mygenelog.com/variants/rs11671010

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