RS514000 Unknown gene

Other Chr 18:12854073
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What This Variant Does
"Implicated in a 2015 Korean cohort for Crohn's disease. [PMID: 25489960]"
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
Crohn's disease C OR: 1.33 9E-8 PubMed
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