Who was studied 123 Japanese ancestry hepatocellular carcinoma cases, 333 Japanese ancestry 5-yr hepatocellular carcinoma-free controls; replicated in 130 Japanese ancestry hepatocellular carcinoma cases, 210 Japanese ancestry 5-yr hepatocellular carcinoma-free controls.
The effect
Each copy of the T allele carried 2.37 times the odds of Hepatocellular carcinoma in post hepatitis C eradication by interferon therapy (95% confidence interval 1.74-3.23); p = 3 × 10−8.
Where it sits Chromosome 4, band 4q32.3 — in an intron of TLL1.
What each result means
A/APublished research associates this genotype with typical/baseline likelihood of Hepatocellular carcinoma in post hepatitis C eradication by interferon therapy — no copies of the reported risk allele.
A/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Hepatocellular carcinoma in post hepatitis C eradication by interferon therapy.
T/TPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Hepatocellular carcinoma in post hepatitis C eradication by interferon therapy compared to the general population.
rs17047200 is a single position in the genome, in or near the TLL1 gene. Published research associates it with hepatocellular carcinoma in post hepatitis c eradication by interferon therapy. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs17047200 linked to?
On MyGeneLog this position is linked to Liver Cancer Risk After Hepatitis C Is Cured. The research behind each link, and its sources, are set out on that condition page.
Does having rs17047200 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 rs17047200 come from?
GWAS Catalog, Gastroenterology 2017, PMID:28163062. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.