GRIN2A · rs11866328
Where this position leads
Condition: Chronic Hepatitis B
Source: GWAS Catalog, Viral Immunol 2011, PMID:22004137
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.
rs11866328 is a single position in the genome, in or near the GRIN2A gene. Published research associates it with hepatitis b. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
On MyGeneLog this position is linked to Chronic Hepatitis B. The research behind each link, and its sources, are set out on that condition page.
Subjects that appear in the title or abstract of the same papers as this rsID include infection and immunity (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
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.
GWAS Catalog, Viral Immunol 2011, PMID:22004137. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.