Standard

Cholesterol, total

TRPS1 · rs2737229

Where this position leads

Condition: Cholesterol (LDL, HDL and Total)

rs2737229 Condition: Cholesterol (LDL, HDL and Total) Cholesterol (LDL, HDL and Total) Condition rs2737229 rs2737229 TRPS1

What the study found

Who was studied 100,184 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 1.11 mg/dL lower (95% confidence interval 0.7-1.52); p = 2 × 10−8.

How common The C allele had a frequency of about 30% in the people studied.

Where it sits Chromosome 8, band 8q23.3 — in an intron of TRPS1.

What each result means

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

What people read about alongside this

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs2737229

What is rs2737229?

rs2737229 is a single position in the genome, in or near the TRPS1 gene. Published research associates it with cholesterol, total. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs2737229 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.

What do people read about alongside rs2737229?

Subjects that appear in the title or abstract of the same papers as this rsID include cholesterol and blood fats (2 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs2737229 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 rs2737229 come from?

GWAS Catalog, Nature 2010, PMID:20686565. 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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Cholesterol, total (rs2737229). MyGeneLog™. https://www.mygenelog.com/variants/rs2737229

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