Sensitive

Coeliac disease

SLC17A1 · rs13213957

Where this position leads

Condition: Celiac Disease

rs13213957 Condition: Celiac Disease Celiac Disease Condition rs13213957 rs13213957 SLC17A1

What the study found

Who was studied 394,626 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.838 higher (95% confidence interval 0.75-0.92); p = 4 × 10−105.

How common The C allele had a frequency of about 10% in the people studied.

Where it sits Chromosome 6, band 6p22.2 — in an intron of SLC17A1.

What each result means

C/C Two copies of the version the research linked to Coeliac disease. 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 Coeliac disease. That is a smaller link than two copies.
T/T No copy of the version the research linked to Coeliac disease. This is the starting point the study compared everyone against.
Source

Questions about rs13213957

What is rs13213957?

rs13213957 is a single position in the genome, in or near the SLC17A1 gene. Published research associates it with coeliac disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs13213957 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 rs13213957 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 rs13213957 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

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Coeliac disease (rs13213957). MyGeneLog™. https://www.mygenelog.com/variants/rs13213957

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