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PDCD6 protein levels

AHRR · rs187007411

Where this position leads

Condition: Celiac Disease

rs187007411 Condition: Celiac Disease Celiac Disease Condition rs187007411 rs187007411 AHRR

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.284 higher (95% confidence interval 0.2-0.37); p = 1 × 10−12.

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

Where it sits Chromosome 5, band 5p15.33 — in an intron of AHRR.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of PDCD6 protein levels compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with PDCD6 protein levels.
G/G Published research associates this genotype with typical/baseline likelihood of PDCD6 protein levels — no copies of the reported risk allele.
Source
A scalable variational inference approach for increased mixed-model association power
Loya H, Kalantzis G, Cooper F, Palamara PF
Nature genetics · 2025 · PMID 39789286 · open access

Questions about rs187007411

What is rs187007411?

rs187007411 is a single position in the genome, in or near the AHRR gene. Published research associates it with pdcd6 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 rs187007411 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 rs187007411 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 rs187007411 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

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

PDCD6 protein levels (rs187007411). MyGeneLog™. https://www.mygenelog.com/variants/rs187007411

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