Moreover, under dominant and recessive models, ADH1B Arg4</span>7His variant genotypes were associated with greater susceptibility to CRC when compared with the wild-type sequence.
Moreover, the SNPs rs1229984 in ADH1B gene was found to be associated with CRC risk: under the recessive model, the OR was 1.75 for A/A genotype (95%CI = 1.21-2.52; p-value = 0.0025).