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FGF2 protein levels

near FGF2 · rs183385653

Where this position leads

Condition: Celiac Disease

rs183385653 Condition: Celiac Disease Celiac Disease Condition rs183385653 rs183385653 near FGF2

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.347 lower (95% confidence interval 0.24-0.46); p = 1 × 10−11.

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

Where it sits Chromosome 4, band 4q28.1 — between genes, 12.8 kb from FGF2.

What each result means

G/G No copy of the version the research linked to FGF2 protein levels. This is the starting point the study compared everyone against.
G/T One copy of the version the research linked to FGF2 protein levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to FGF2 protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs183385653

What is rs183385653?

rs183385653 is a single position in the genome, in or near the near FGF2 gene. Published research associates it with fgf2 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 rs183385653 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 rs183385653 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 rs183385653 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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FGF2 protein levels (rs183385653). MyGeneLog™. https://www.mygenelog.com/variants/rs183385653

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