Sensitive

Type 1 diabetes

KIAA0350 · rs12708716

Where this position leads

Condition: Type 1 Diabetes

rs12708716 Condition: Type 1 Diabetes Type 1 Diabetes Condition rs12708716 rs12708716 KIAA0350

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Type 1 diabetes compared to the general population. (GWAS Catalog, Nat Genet 2007, PMID:17554260)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Type 1 diabetes. (GWAS Catalog, Nat Genet 2007, PMID:17554260)
G/G Published research associates this genotype with typical/baseline likelihood of Type 1 diabetes — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2007, PMID:17554260)

Source: GWAS Catalog, Nat Genet 2007, PMID:17554260

What people read about alongside this

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 rs12708716

What is rs12708716?

rs12708716 is a single position in the genome, in or near the KIAA0350 gene. Published research associates it with type 1 diabetes. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs12708716 linked to?

On MyGeneLog this position is linked to Type 1 Diabetes. The research behind each link, and its sources, are set out on that condition page.

What do people read about alongside rs12708716?

Subjects that appear in the title or abstract of the same papers as this rsID include gut and food intolerance (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 rs12708716 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 rs12708716 come from?

GWAS Catalog, Nat Genet 2007, PMID:17554260. 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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