C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Type 2 diabetes compared to the general population.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Type 2 diabetes.
T/TPublished research associates this genotype with typical/baseline likelihood of Type 2 diabetes — no copies of the reported risk allele.
Nature communications · 2018 · PMID 30054458 · open access
Questions about rs7845219
What is rs7845219?
rs7845219 is a single position in the genome, in or near the TP53INP1 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 rs7845219 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.
Does having rs7845219 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 rs7845219 come from?
GWAS Catalog, Nat Commun 2018, PMID:30054458. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.