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FGF23 protein levels

near FGF23 · rs6489536

Where this position leads

Condition: Celiac Disease

rs6489536 Condition: Celiac Disease Celiac Disease Condition rs6489536 rs6489536 near FGF23

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0858 higher (95% confidence interval 0.074-0.098); p = 4 × 10−51.

How common The C allele had a frequency of about 34% in the people studied.

Where it sits Chromosome 12, band 12p13.32 — between genes, 3 kb from FGF23.

What each result means

C/C Two copies of the version the research linked to FGF23 protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/G One copy of the version the research linked to FGF23 protein levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to FGF23 protein levels. This is the starting point the study compared everyone against.
Source

Questions about rs6489536

What is rs6489536?

rs6489536 is a single position in the genome, in or near the near FGF23 gene. Published research associates it with fgf23 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 rs6489536 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 rs6489536 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 rs6489536 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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FGF23 protein levels (rs6489536). MyGeneLog™. https://www.mygenelog.com/variants/rs6489536

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