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C1RL protein levels

CLSTN3 · rs113899462

Where this position leads

Condition: Celiac Disease

rs113899462 Condition: Celiac Disease Celiac Disease Condition rs113899462 rs113899462 CLSTN3

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.302 lower (95% confidence interval 0.27-0.33); p = 3 × 10−103.

How common The A allele had a frequency of about 4% in the people studied.

Where it sits Chromosome 12, band 12p13.31 — in an intron of CLSTN3.

What each result means

A/A Two copies of the version the research linked to C1RL 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 C1RL protein levels. That is a smaller link than two copies.
G/G No copy of the version the research linked to C1RL protein levels. This is the starting point the study compared everyone against.
Source

Questions about rs113899462

What is rs113899462?

rs113899462 is a single position in the genome, in or near the CLSTN3 gene. Published research associates it with c1rl 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 rs113899462 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 rs113899462 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 rs113899462 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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C1RL protein levels (rs113899462). MyGeneLog™. https://www.mygenelog.com/variants/rs113899462

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