Table 3 Relationship between rs3731249 and risk of developing ALL subtypes.

From: The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A

ALL Subtype

rs3731249 genotypes (CC/CT/TT)

RAFa in controls

P-valued

Cases

ETV6-RUNX1

122/14/1

0.02

0.78

Hyperdiploid

153/16/0

0.02

–

  1. aRAF: risk allele frequency. bOR: odds ratio and cCI: confidence intervals.
  2. dP-value from stratified analysis.
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