Sensitive

Celiac disease

IL12A · rs17810546

Where this position leads

Condition: Celiac Disease

rs17810546 Condition: Celiac Disease Celiac Disease Condition Topic: Gut and food intolerance Gut and food intolerance Topic rs17810546 rs17810546 IL12A

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Celiac disease — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2008, PMID:18311140)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Celiac disease. (GWAS Catalog, Nat Genet 2008, PMID:18311140)
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Celiac disease compared to the general population. (GWAS Catalog, Nat Genet 2008, PMID:18311140)

Source: GWAS Catalog, Nat Genet 2008, PMID:18311140

What people read about alongside this

Gut and food intolerance4

Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.

Questions about rs17810546

What is rs17810546?

rs17810546 is a single position in the genome, in or near the IL12A gene. Published research associates it with celiac 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 rs17810546 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.

What do people read about alongside rs17810546?

Subjects that appear in the title or abstract of the same papers as this rsID include gut and food intolerance (4 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs17810546 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 rs17810546 come from?

GWAS Catalog, Nat Genet 2008, PMID:18311140. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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