3 5522635222229Reads by AI crawlersClaude2ChatGPT2Google · Gemini6Perplexity3Meta AI5Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others29Total55Counted 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 767 European ancestry cases, 1,422 European ancestry controls; replicated in 1,643 European ancestry cases, 3,406 European ancestry controls.
The effect
Each copy of the G allele carried 1.35 times the odds of Celiac disease (95% confidence interval 1.23-1.49); p = 1 × 10−9.
Where it sits Chromosome 3, band 3q25.33 — in an intron of IL12A-AS1.
What each result means
A/ANo copy of the version the research linked to Celiac disease. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Celiac disease. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Celiac 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 rs17810546
What is rs17810546?
rs17810546 is a single position in the genome, in or near the IL12A gene. Published research associates it with celiac 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 rs17810546 linked to?
On MyGeneLog this position is linked to Celiac Disease. The research behind each link, and its sources, are set out on that condition page.
What do people read about alongside rs17810546?
Subjects that appear in the title or abstract of the same papers as this rsID include gut and food intolerance (4 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs17810546 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 rs17810546 come from?
GWAS Catalog, Nat Genet 2008, PMID:18311140. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
3 5522635222229Reads by AI crawlersClaude2ChatGPT2Google · Gemini6Perplexity3Meta AI5Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others29Total55Counted 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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