C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Crohn's disease-related phenotypes compared to the general population. (GWAS Catalog, Gastroenterology 2014, PMID:25557950)
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Crohn's disease-related phenotypes. (GWAS Catalog, Gastroenterology 2014, PMID:25557950)
T/TPublished research associates this genotype with typical/baseline likelihood of Crohn's disease-related phenotypes — no copies of the reported risk allele. (GWAS Catalog, Gastroenterology 2014, PMID:25557950)
rs11924265 is a single position in the genome, in or near the MAGI1 gene. Published research associates it with crohn's disease-related phenotypes. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs11924265 linked to?
On MyGeneLog this position is linked to Crohn's Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs11924265 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 rs11924265 come from?
GWAS Catalog, Gastroenterology 2014, PMID:25557950. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.