Sensitive

Type 1 diabetes

IL2RA · rs10795791

Where this position leads

Condition: Type 1 Diabetes

rs10795791 Condition: Type 1 Diabetes Type 1 Diabetes Condition rs10795791 rs10795791 IL2RA

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Type 1 diabetes — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2015, PMID:25751624)
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 2015, PMID:25751624)
G/G 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 2015, PMID:25751624)

Source: GWAS Catalog, Nat Genet 2015, PMID:25751624

Questions about rs10795791

What is rs10795791?

rs10795791 is a single position in the genome, in or near the IL2RA 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 rs10795791 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.

Does having rs10795791 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 rs10795791 come from?

GWAS Catalog, Nat Genet 2015, PMID:25751624. 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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