Table 3

Relationship between SNP mapping within 25 kb of EPOR and BCP-ALL risk

SNPLocation, bpAncestral alleleETV6-RUNX1-positive cases
Hyperdiploid cases
Other cases
Odds ratioPOdds ratioPOdds ratioP
rs7251786 11 325 879 1.16 .264 1.04 .675 0.94 .416 
rs318699 11 362 240 1.11 .423 1.12 .207 1.02 .818 
rs4804164 11 363 291 0.58 .008 0.92 .588 0.97 .838 
rs2291516 11 369 177 0.83 .409 1.10 .526 1.03 .827 
rs317913 11 373 314 0.60 .019 0.97 .850 0.94 .680 
SNPLocation, bpAncestral alleleETV6-RUNX1-positive cases
Hyperdiploid cases
Other cases
Odds ratioPOdds ratioPOdds ratioP
rs7251786 11 325 879 1.16 .264 1.04 .675 0.94 .416 
rs318699 11 362 240 1.11 .423 1.12 .207 1.02 .818 
rs4804164 11 363 291 0.58 .008 0.92 .588 0.97 .838 
rs2291516 11 369 177 0.83 .409 1.10 .526 1.03 .827 
rs317913 11 373 314 0.60 .019 0.97 .850 0.94 .680 

Odds ratios were calculated with the ancestral allele as the reference allele, and P values are from the Cochran-Armitage trend test.

SNP indicates single nucleotide polymorphism; and BCP-ALL, B-cell precursor acute lymphoblastic leukemia.

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