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Who was studied 6,687 European ancestry cases, 19,718 European ancestry controls; replicated in 9,628 European ancestry cases, 12,917 European ancestry controls.
The effect
Each copy of the C allele carried 1.16 times the odds of Ulcerative colitis (95% confidence interval 1.10-1.21); p = 1 × 10−16.
How common The C allele had a frequency of about 18% in the people studied.
Where it sits Chromosome 13, band 13q12.13 — between genes, 20.4 kb from RPS21P8.
What each result means
C/CTwo copies of the version the research linked to Ulcerative colitis. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Ulcerative colitis. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Ulcerative colitis. This is the starting point the study compared everyone against.
Nature genetics · 2011 · PMID 21297633 · open access
Questions about rs17085007
What is rs17085007?
rs17085007 is a single position in the genome, in or near the near USP12 gene. Published research associates it with ulcerative colitis. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs17085007 linked to?
On MyGeneLog this position is linked to Ulcerative Colitis. The research behind each link, and its sources, are set out on that condition page.
Does having rs17085007 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 rs17085007 come from?
GWAS Catalog, Nat Genet 2011, PMID:21297633. 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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