Sensitive

Pediatric autoimmune diseases

FUT2 · rs602662

Where this position leads

Condition: Ulcerative Colitis

rs602662 Condition: Ulcerative Colitis Ulcerative Colitis Condition rs602662 FUT2

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Pediatric autoimmune diseases — no copies of the reported risk allele. (GWAS Catalog, Nat Med 2015, PMID:26301688)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Pediatric autoimmune diseases. (GWAS Catalog, Nat Med 2015, PMID:26301688)
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Pediatric autoimmune diseases compared to the general population. (GWAS Catalog, Nat Med 2015, PMID:26301688)

Source: GWAS Catalog, Nat Med 2015, PMID:26301688

What people read about alongside this

Longevity and ageing1

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 rs602662

What is rs602662?

rs602662 is a single position in the genome, in or near the FUT2 gene. Published research associates it with pediatric autoimmune diseases. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs602662 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 rs602662?

Subjects that appear in the title or abstract of the same papers as this rsID include longevity and ageing (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.

Does having rs602662 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 rs602662 come from?

GWAS Catalog, Nat Med 2015, PMID:26301688. 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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