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CHRDL2 protein levels

near POLD3 · rs7104802

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.16 higher (95% confidence interval 0.15-0.17); p = 6 × 10−184.

How common The T allele had a frequency of about 41% in the people studied.

Where it sits Chromosome 11, band 11q13.4 — between genes, 6.6 kb from POLD3.

What each result means

G/G Published research associates this genotype with typical/baseline likelihood of CHRDL2 protein levels — no copies of the reported risk allele.
G/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with CHRDL2 protein levels.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of CHRDL2 protein levels compared to the general population.
Source

Questions about rs7104802

What is rs7104802?

rs7104802 is a single position in the genome, in or near the near POLD3 gene. Published research associates it with chrdl2 protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs7104802 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 rs7104802 come from?

GWAS Catalog, Nature genetics 2025, PMID:39789286. 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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CHRDL2 protein levels (rs7104802). MyGeneLog™. https://www.mygenelog.com/variants/rs7104802

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