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PXN protein levels

near HLA-DQB1 · rs28414666

Where this position leads

Condition: Celiac Disease

rs28414666 Condition: Celiac Disease Celiac Disease Condition rs28414666 rs28414666 near HLA-DQB1

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0514 higher (95% confidence interval 0.039-0.064); p = 3 × 10−18.

How common The A allele had a frequency of about 21% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — between genes, 0.8 kb from HLA-DQB1.

What each result means

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

Questions about rs28414666

What is rs28414666?

rs28414666 is a single position in the genome, in or near the near HLA-DQB1 gene. Published research associates it with pxn 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 rs28414666 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 rs28414666 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 rs28414666 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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PXN protein levels (rs28414666). MyGeneLog™. https://www.mygenelog.com/variants/rs28414666

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