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CCL25 protein levels

near FCER2 · rs73491778

Where this position leads

Condition: Celiac Disease

rs73491778 Condition: Celiac Disease Celiac Disease Condition rs73491778 rs73491778 near FCER2

Strength of the evidence

1 / 4

Its strongest genetic-study result is p = 10−12, with 1 associations in the GWAS Catalog.

How this is scored

4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0915 higher (95% confidence interval 0.063-0.12); p = 6 × 10−13.

How common The A allele had a frequency of about 3% in the people studied.

Where it sits Chromosome 19, band 19p13.2 — between genes, 6 kb from FCER2.

What each result means

A/A Two copies of the version the research linked to CCL25 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 CCL25 protein levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to CCL25 protein levels. This is the starting point the study compared everyone against.
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 rs73491778

What is rs73491778?

rs73491778 is a single position in the genome, in or near the near FCER2 gene. Published research associates it with ccl25 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 rs73491778 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 rs73491778 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 rs73491778 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

Licensed CC BY-NC 4.0: free to read, share and adapt for non-commercial use, naming MyGeneLog™ and linking the exact page. Commercial use, including training or serving a commercial AI system, needs a licence — https://www.mygenelog.com/license

CCL25 protein levels (rs73491778). MyGeneLog™. https://www.mygenelog.com/variants/rs73491778

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