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Triglyceride percentage of total lipids in intermediate-density lipoprotein

P2RX3 · rs11229003

What the study found

Who was studied 199,732 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.034 higher (95% confidence interval 0.025-0.043); p = 2 × 10−12.

How common The A allele had a frequency of about 11% in the people studied.

Where it sits Chromosome 11, band 11q12.1 — in an intron of P2RX3.

What each result means

A/A Two copies of the version the research linked to Triglyceride percentage of total lipids in intermediate-density lipoprotein. 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 Triglyceride percentage of total lipids in intermediate-density lipoprotein. That is a smaller link than two copies.
G/G No copy of the version the research linked to Triglyceride percentage of total lipids in intermediate-density lipoprotein. This is the starting point the study compared everyone against.
Source

Questions about rs11229003

What is rs11229003?

rs11229003 is a single position in the genome, in or near the P2RX3 gene. Published research associates it with triglyceride percentage of total lipids in intermediate-density lipoprotein. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11229003 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 rs11229003 come from?

GWAS Catalog, British journal of cancer 2025, PMID:40307439. 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 percentage of total lipids in intermediate-density lipoprotein (rs11229003). MyGeneLog™. https://www.mygenelog.com/variants/rs11229003

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