C/CPublished research associates this genotype with typical/baseline likelihood of Primary biliary cholangitis — no copies of the reported risk allele.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Primary biliary cholangitis.
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Primary biliary cholangitis compared to the general population.
rs1889341 is a single position in the genome, in or near the near ZNF217 gene. Published research associates it with primary biliary cholangitis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs1889341 linked to?
On MyGeneLog this position is linked to Primary Biliary Cholangitis. The research behind each link, and its sources, are set out on that condition page.
Does having rs1889341 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 rs1889341 come from?
GWAS Catalog, Hepatology (Baltimore, Md.) 2024, PMID:38652555. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.