RS1551398 Unknown gene

Other Chr 8:125527809
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What This Variant Does
"DeCode reports that rs1551398 is associated with susceptibility to Crohn's disease. [GWAS:Crohn's d..."
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Crohn's disease A OR: 1.08 5E-9 PubMed
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