Sensitive

Crohn's disease

Unknown · rs3764147

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Where this position leads

Condition: Crohn's Disease

rs3764147 Condition: Crohn's Disease Crohn's Disease Condition rs3764147 Unknown

What each result means

A/A Published research associates this genotype with typical/baseline likelihood of Crohn's disease — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2008, PMID:18587394)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Crohn's disease. (GWAS Catalog, Nat Genet 2008, PMID:18587394)
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Crohn's disease compared to the general population. (GWAS Catalog, Nat Genet 2008, PMID:18587394)

Source: GWAS Catalog, Nat Genet 2008, PMID:18587394

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