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STC1 protein levels

CD209 · rs11465422

Where this position leads

Condition: Celiac Disease

rs11465422 Condition: Celiac Disease Celiac Disease Condition rs11465422 rs11465422 CD209

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0756 lower (95% confidence interval 0.054-0.098); p = 1 × 10−12.

How common The T allele had a frequency of about 7% in the people studied.

Where it sits Chromosome 19, band 19p13.2 — in the 3′ untranslated region of CD209.

What each result means

C/C No copy of the version the research linked to STC1 protein levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to STC1 protein levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to STC1 protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs11465422

What is rs11465422?

rs11465422 is a single position in the genome, in or near the CD209 gene. Published research associates it with stc1 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 rs11465422 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 rs11465422 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 rs11465422 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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STC1 protein levels (rs11465422). MyGeneLog™. https://www.mygenelog.com/variants/rs11465422

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