Unknown · rs3764147
Where this position leads
Condition: Crohn's Disease
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 G allele carried 1.25 times the odds of Crohn's disease; p = 2 × 10−13.
How common The G allele had a frequency of about 22% in the people studied.
Where it sits Chromosome 13, band 13q14.11 — a missense change in LACC1.
What ClinVar records
Classification
Benign for Juvenile arthritis due to defect in LACC1, Leprosy, susceptibility to, 1; criteria provided, multiple submitters, no conflicts (2 of 4 stars, 5 submitters), last evaluated 2024-01-24.
ClinVar record 1300105 NM_153218.4(LACC1):c.760A>G (p.Ile254Val)
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 people read about alongside this
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.
rs3764147 is a single position in the genome, in or near the Unknown 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.
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.
Subjects that appear in the title or abstract of the same papers as this rsID include infection and immunity (2 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
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.
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.
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Crohn's disease (rs3764147). MyGeneLog™. https://www.mygenelog.com/variants/rs3764147