Sensitive

Type 2 diabetes

JAZF1 · rs864745

Where this position leads

Condition: Type 2 Diabetes

rs864745 Condition: Type 2 Diabetes Type 2 Diabetes Condition rs864745 rs864745 JAZF1

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Type 2 diabetes — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2008, PMID:18372903)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Type 2 diabetes. (GWAS Catalog, Nat Genet 2008, PMID:18372903)
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Type 2 diabetes compared to the general population. (GWAS Catalog, Nat Genet 2008, PMID:18372903)

Source: GWAS Catalog, Nat Genet 2008, PMID:18372903

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 rs864745

What is rs864745?

rs864745 is a single position in the genome, in or near the JAZF1 gene. Published research associates it with type 2 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 rs864745 linked to?

On MyGeneLog this position is linked to Type 2 Diabetes. The research behind each link, and its sources, are set out on that condition page.

What do people read about alongside rs864745?

Subjects that appear in the title or abstract of the same papers as this rsID include brain and memory (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 rs864745 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 rs864745 come from?

GWAS Catalog, Nat Genet 2008, PMID:18372903. 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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