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PTPRB protein levels

PRANCR · rs117462747

Where this position leads

Condition: Celiac Disease

rs117462747 Condition: Celiac Disease Celiac Disease Condition rs117462747 rs117462747 PRANCR

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.147 higher (95% confidence interval 0.1-0.19); p = 1 × 10−12.

How common The A allele had a frequency of about 2% in the people studied.

Where it sits Chromosome 12, band 12q15 — in an intron of PRANCR.

What each result means

A/A Two copies of the version the research linked to PTPRB protein levels. 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 PTPRB protein levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to PTPRB protein levels. This is the starting point the study compared everyone against.
Source

Questions about rs117462747

What is rs117462747?

rs117462747 is a single position in the genome, in or near the PRANCR gene. Published research associates it with ptprb 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 rs117462747 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 rs117462747 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 rs117462747 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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PTPRB protein levels (rs117462747). MyGeneLog™. https://www.mygenelog.com/variants/rs117462747

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