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CXCL17 protein levels

SBNO2 · rs4807612

Where this position leads

Condition: Celiac Disease

rs4807612 Condition: Celiac Disease Celiac Disease Condition rs4807612 rs4807612 SBNO2

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.054 lower (95% confidence interval 0.044-0.064); p = 9 × 10−30.

How common The C allele had a frequency of about 32% in the people studied.

Where it sits Chromosome 19, band 19p13.3 — in an intron of SBNO2.

What each result means

C/C Two copies of the version the research linked to CXCL17 protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/T One copy of the version the research linked to CXCL17 protein levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to CXCL17 protein levels. This is the starting point the study compared everyone against.
Source

Questions about rs4807612

What is rs4807612?

rs4807612 is a single position in the genome, in or near the SBNO2 gene. Published research associates it with cxcl17 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 rs4807612 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 rs4807612 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 rs4807612 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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CXCL17 protein levels (rs4807612). MyGeneLog™. https://www.mygenelog.com/variants/rs4807612

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