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GLIPR1 protein levels

MACROD2 · rs566462617

Where this position leads

Condition: Celiac Disease

rs566462617 Condition: Celiac Disease Celiac Disease Condition rs566462617 rs566462617 MACROD2

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.714 lower (95% confidence interval 0.52-0.91); p = 8 × 10−12.

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

Where it sits Chromosome 20, band 20p12.1 — in an intron of MACROD2.

What each result means

C/C 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.
C/T One copy of the version the research linked to GLIPR1 protein levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to GLIPR1 protein levels. This is the starting point the study compared everyone against.
Source

Questions about rs566462617

What is rs566462617?

rs566462617 is a single position in the genome, in or near the MACROD2 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 rs566462617 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 rs566462617 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 rs566462617 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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GLIPR1 protein levels (rs566462617). MyGeneLog™. https://www.mygenelog.com/variants/rs566462617

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