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. 2013 Aug 22;8(8):e72557. doi: 10.1371/journal.pone.0072557

Table 2. Association between xMHC genetic variants and BCP-ALL in children.

Frequencya
Single SNP
Mutually adjusted
SNP Position Region of xMHC Minor allele Cases Controls OR 95% CIb p-value OR 95% CIb p-value p-value (FWE) c
rs7747023 29133659 Extended class I G 0.17 0.21 0.73 (0.60-0.89) 1.7x10-3 0.72 (0.59-0.88) 1.4x10-3 0.518
rs3130785 30904717 Class I A 0.14 0.11 1.45 (1.16-1.82) 1.3x10-3 1.37 (1.09-1.74) 7.9x10-3 0.973
rs1632856 31079715 Class I A 0.25 0.29 0.80 (0.68-0.95) 9.9x10-3 0.79 (0.66-0.94) 8.6x10-3 0.898
rs2524279 31500885 Class I G 0.11 0.15 0.73 (0.58-0.92) 7.9 x10-3 0.70 (0.55-0.89) 3.0x10-3 0.749
rs9296068 33096673 Class II C 0.42 0.36 1.37 (1.17-1.61) 1.2x10-4 1.40 (1.19-1.66) 5.7x10-5 0.036
rs213203d 33346382 Extended class II A 0.47 0.49 0.68 (0.55-0.84) 3.6x10-4 0.69 (0.55-0.86) 7.4x10-4 0.347

Abbreviations: CI, confidence interval; FWE, family-wise type I error; OR, odds ratio; SNP, single nucleotide polymorphism; xMHC, extended major histocompatibility complex

a Frequency of the minor allele in case and control subjects

b ORs and 95% CI for each SNP in the single SNP analysis were derived using logistic regression assuming a log-additive genetic model of inheritance and adjusting for child’s age, sex, and race/ethnicity (non-Hispanic white versus Hispanic). The mutually adjusted analysis included additional adjustment for the effects of all other SNPs in the table.

c Adjustment for multiple testing was performed with 10,000 permutations of case-control status on 1,145 SNPs and using FWE rate of 0.05. An adjusted p-value of less than 0.05 was considered statistically significant.

d Evaluation of the genetic model of inheritance indicated a significant deviation from the log-additive model with an effect associated with heterozygotes. ORs and 95% CI were estimated for heterozygous genotypes compared to homozygous genotypes.