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Who was studied 811 European ancestry cases, 4,654 European ancestry controls.
The effect
Each copy of the T allele carried 3.41 times the odds of Biliary atresia (95% confidence interval 2.99-3.82); p = 7 × 10−9.
Where it sits Chromosome 10, band 10p15.1 — in an intron of LINC00705.
What each result means
C/CNo copy of the version the research linked to Biliary atresia. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Biliary atresia. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Biliary atresia. That is the strongest link of the three results. A link in a study is not a diagnosis.
Journal of hepatology · 2023 · PMID 37572794 · open access
Questions about rs2083872
What is rs2083872?
rs2083872 is a single position in the genome, in or near the LINC00705 gene. Published research associates it with biliary atresia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs2083872 linked to?
On MyGeneLog this position is linked to Biliary Atresia. The research behind each link, and its sources, are set out on that condition page.
Does having rs2083872 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 rs2083872 come from?
GWAS Catalog, Journal of hepatology 2023, PMID:37572794. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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