6 5842638222227Reads by AI crawlersClaude4ChatGPT2Google · Gemini6Perplexity3Meta AI8Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others27Total58Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Solid lines are connections this site curates. Dashed lines mean the two ends share a research paper — worth knowing, and not a claim that one explains the other.
What the study found
Who was studied 3,230 European ancestry cases, 4,829 European ancestry controls; replicated in 1,339 European ancestry trios, 2,325 European ancestry cases, 1,809 European ancestry controls.
The effect
Each copy of the T allele carried 1.16 times the odds of Crohn's disease; p = 1 × 10−9.
How common The T allele had a frequency of about 39% in the people studied.
Where it sits Chromosome 11, band 11q13.5 — between genes, 17.1 kb from LINC02757.
What each result means
C/CNo copy of the version the research linked to Crohn's disease. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Crohn's disease. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Crohn's disease. That is the strongest link of the three results. A link in a study is not a diagnosis.
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.
Questions about rs7927894
What is rs7927894?
rs7927894 is a single position in the genome, in or near the C11orf30 gene. Published research associates it with crohn's disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7927894 linked to?
On MyGeneLog this position is linked to Crohn's Disease. The research behind each link, and its sources, are set out on that condition page.
What do people read about alongside rs7927894?
Subjects that appear in the title or abstract of the same papers as this rsID include allergies (9 papers), gut and food intolerance (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs7927894 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 rs7927894 come from?
GWAS Catalog, Nat Genet 2008, PMID:18587394. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
6 5842638222227Reads by AI crawlersClaude4ChatGPT2Google · Gemini6Perplexity3Meta AI8Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others27Total58Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
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