RS9292777 Unknown gene

Other Chr 5:40437846
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What This Variant Does
"rs9292777 is in linkage disequilibrium with a polymorphism that increases susceptibility to Crohn's ..."
GWAS Studies (3)
Trait Risk Allele OR / Beta P-value Study
Crohn's disease — OR: 1.34 3E-18 PubMed
Crohn's disease T OR: 1.37 2E-11 PubMed
Multiple sclerosis T OR: 1.19 1E-9 PubMed
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