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GLIPR1 protein levels

LINC01470 · rs564634150

Where this position leads

Condition: Celiac Disease

rs564634150 Condition: Celiac Disease Celiac Disease Condition rs564634150 rs564634150 LINC01470

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.517 higher (95% confidence interval 0.36-0.67); p = 6 × 10−12.

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

Where it sits Chromosome 5, band 5q33.1 — in an intron of LINC01470.

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 rs564634150

What is rs564634150?

rs564634150 is a single position in the genome, in or near the LINC01470 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 rs564634150 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 rs564634150 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 rs564634150 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 (rs564634150). MyGeneLog™. https://www.mygenelog.com/variants/rs564634150

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