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Who was studied 97 European ancestry thyroiditis cases, 107 European ancestry ankylosing spondylitis cases, 100 European ancestry psoriasis cases, 173 European ancestry celiac disease cases, 254 European ancestry systemic lupus erythematosus cases, 308 European ancestry common variable inmunodeficiency cases, 865 European ancestry ulcerative colitis cases, 1,086 European ancestry Type 1 diabetes cases, 1,123 European ancestry juvenile idiopathic arthritis cases, 1,922 European ancestry Crohn's disease cases, 10,718 European ancestry controls.
The effect
The reported allele is G; the catalogue records no effect size
; p = 8 × 10−11.
How common The G allele had a frequency of about 31% in the people studied.
Where it sits Chromosome 3, band 3p21.31 — in the 3′ untranslated region of BSN-DT.
What ClinVar records
Classificationnot provided; no classification provided (0 of 4 stars, 1 submitter), last evaluated 2011-05-13.
ClinVar record 31759NM_004393.6(DAG1):c.*1508A>G
What this is ClinVar's aggregate record for this position (as of its 2026-10-19 release), not a result about you. A classification describes the variant against the condition named, as laboratories submitted it. Whether a person carries this variant, and what that would mean for them, is a question for a clinical test and a genetic counsellor.
What each result means
A/ANo copy of the version the research linked to Pediatric autoimmune diseases. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Pediatric autoimmune diseases. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Pediatric autoimmune diseases. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs4625 is a single position in the genome, in or near the DAG1 gene. Published research associates it with pediatric autoimmune diseases. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs4625 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 rs4625 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 rs4625 come from?
GWAS Catalog, Nat Med 2015, PMID:26301688. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
2 353219323210Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity1Meta AI9Microsoft · Copilot3Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others10Total35Counted 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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