Sensitive

Celiac disease (PheCode 557.1)

TSBP1-AS1 · rs113857285

Where this position leads

Condition: Celiac Disease

rs113857285 Condition: Celiac Disease Celiac Disease Condition rs113857285 rs113857285 TSBP1-AS1

What the study found

Who was studied 1,036 European ancestry cases, 455,312 European ancestry controls.

The effect Each copy of the A allele shifted the measure 4.04 higher (95% confidence interval 2.75-5.33); p = 8 × 10−10.

How common The A allele had a frequency of about 0% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — in an intron of TSBP1-AS1.

What each result means

A/A Two copies of the version the research linked to Celiac disease (PheCode 557.1). 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 Celiac disease (PheCode 557.1). That is a smaller link than two copies.
G/G No copy of the version the research linked to Celiac disease (PheCode 557.1). This is the starting point the study compared everyone against.
Source

Questions about rs113857285

What is rs113857285?

rs113857285 is a single position in the genome, in or near the TSBP1-AS1 gene. Published research associates it with celiac disease (phecode 557.1). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs113857285 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 rs113857285 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 rs113857285 come from?

GWAS Catalog, Nature genetics 2021, PMID:34737426. 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.

Celiac disease (PheCode 557.1) (rs113857285). MyGeneLog™. https://www.mygenelog.com/variants/rs113857285

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