RS3810936 Unknown gene

Other Chr 9:114790605
Upload your DNA to see your genotype for this variant.
What This Variant Does
"Associated with increased risk for Crohn's disease in a study of 380 Korean patients. [OMIM:INFLAMM..."
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Crohn's disease C OR: 1.21 1E-15 PubMed
Ask Dr. Hemsworth about this variant