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Ulcerative colitis

PUS10 · rs13003464

Where this position leads

Condition: Ulcerative Colitis

rs13003464 Condition: Ulcerative Colitis Ulcerative Colitis Condition rs13003464 PUS10

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Ulcerative colitis — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2010, PMID:20228799)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Ulcerative colitis. (GWAS Catalog, Nat Genet 2010, PMID:20228799)
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Ulcerative colitis compared to the general population. (GWAS Catalog, Nat Genet 2010, PMID:20228799)

Source: GWAS Catalog, Nat Genet 2010, PMID:20228799

What people read about alongside this

Gut and food intolerance2

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 rs13003464

What is rs13003464?

rs13003464 is a single position in the genome, in or near the PUS10 gene. Published research associates it with ulcerative colitis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs13003464 linked to?

On MyGeneLog this position is linked to Ulcerative Colitis. The research behind each link, and its sources, are set out on that condition page.

What do people read about alongside rs13003464?

Subjects that appear in the title or abstract of the same papers as this rsID include gut and food intolerance (2 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs13003464 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 rs13003464 come from?

GWAS Catalog, Nat Genet 2010, PMID:20228799. 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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