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GLIPR1 protein levels

near Y_RNA · rs569725477

Where this position leads

Condition: Celiac Disease

rs569725477 Condition: Celiac Disease Celiac Disease Condition rs569725477 rs569725477 near Y_RNA

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.541 higher (95% confidence interval 0.39-0.7); p = 4 × 10−12.

How common The G allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 4, band 4q32.1 — between genes, 25.9 kb from Y_RNA.

What each result means

A/A No copy of the version the research linked to GLIPR1 protein levels. This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to GLIPR1 protein levels. That is a smaller link than two copies.
G/G Two copies of the version the research linked to GLIPR1 protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs569725477

What is rs569725477?

rs569725477 is a single position in the genome, in or near the near Y_RNA gene. Published research associates it with glipr1 protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs569725477 linked to?

On MyGeneLog this position is linked to Celiac Disease. The research behind each link, and its sources, are set out on that condition page.

Does having rs569725477 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 rs569725477 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.

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GLIPR1 protein levels (rs569725477). MyGeneLog™. https://www.mygenelog.com/variants/rs569725477

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