RS4613763 Unknown gene

Other Chr 5:40392626
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What This Variant Does
"rs4613763 increases susceptibility to Crohn's disease 1.56 times for carriers of the C allele [OMIM..."
GWAS Studies (2)
Trait Risk Allele OR / Beta P-value Study
Crohn's disease C OR: 1.32 7E-27 PubMed
Multiple sclerosis G OR: 1.2 3E-16 PubMed
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