RS1373692 Unknown gene

Other Chr 5:40431081
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What This Variant Does
"rs1373692 increases susceptibility to Crohn's disease 1.46 times for carriers of the G allele [OMIM..."
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Crohn's disease OR: 1.46 2E-12 PubMed
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