C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Celiac disease compared to the general population.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Celiac disease.
T/TPublished research associates this genotype with typical/baseline likelihood of Celiac disease — no copies of the reported risk allele.
European journal of human genetics : EJHG · 2020 · PMID 31591516
Questions about rs9610686
What is rs9610686?
rs9610686 is a single position in the genome, in or near the RAC2 gene. Published research associates it with celiac disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs9610686 linked to?
On MyGeneLog this position is linked to Celiac Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs9610686 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 rs9610686 come from?
GWAS Catalog, Eur J Hum Genet 2019, PMID:31591516. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.