RS17756311 Unknown gene

Other Chr 9:22053896
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What This Variant Does
"Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnica..."
GWAS Studies (1)
Trait Risk Allele OR / Beta P-value Study
B-cell lymphoblastic leukemia or Crohn's disease (pleiotropy) 8E-10 PubMed
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