RS7746082 Unknown gene

Other Chr 6:105987394
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What This Variant Does
"DeCode reports that rs7746082 is associated with susceptibility to Crohn's disease. An investigation..."
GWAS Studies (5)
Trait Risk Allele OR / Beta P-value Study
Crohn's disease C OR: 1.14 3E-23 PubMed
Inflammatory bowel disease — — 9E-13 PubMed
Crohn's disease — — 2E-12 PubMed
Crohn's disease C OR: 1.17 2E-10 PubMed
Ulcerative colitis C OR: 1.08 2E-7 PubMed
Ask Dr. Hemsworth about this variant