A/APublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Epstein Barr virus nuclear antigen 1 IgG levels or multiple sclerosis compared to the general population.
A/CPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Epstein Barr virus nuclear antigen 1 IgG levels or multiple sclerosis.
C/CPublished research associates this genotype with typical/baseline likelihood of Epstein Barr virus nuclear antigen 1 IgG levels or multiple sclerosis — no copies of the reported risk allele.
rs11808092 is a single position in the genome, in or near the EVI5 gene. Published research associates it with epstein barr virus nuclear antigen 1 igg levels or multiple sclerosis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs11808092 linked to?
On MyGeneLog this position is linked to Multiple Sclerosis. The research behind each link, and its sources, are set out on that condition page.
Does having rs11808092 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 rs11808092 come from?
GWAS Catalog, Mult Scler 2016, PMID:26819262. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.