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CPVL protein levels

FUT8 · rs2149839

Where this position leads

Condition: Celiac Disease

rs2149839 Condition: Celiac Disease Celiac Disease Condition rs2149839 rs2149839 FUT8

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0216 lower (95% confidence interval 0.014-0.029); p = 2 × 10−12.

How common The A allele had a frequency of about 68% in the people studied.

Where it sits Chromosome 14, band 14q23.3 — in an intron of FUT8.

What each result means

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

Questions about rs2149839

What is rs2149839?

rs2149839 is a single position in the genome, in or near the FUT8 gene. Published research associates it with cpvl 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 rs2149839 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 rs2149839 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 rs2149839 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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CPVL protein levels (rs2149839). MyGeneLog™. https://www.mygenelog.com/variants/rs2149839

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