Table 3

Association between activating KIR genes and risk for B-ALL in white patients of Canadian non-French ancestry

GenePatients (n = 45), n (%)Control subjects (n = 245), n (%)OR (95% CI)zP
2DS1 5 (11.1) 102 (41.6) 0.18 (0.07-0.46) −3.54 4.0 × 10−4 
2DS2 10 (22.2) 138 (56.3) 0.22 (0.10-0.47) −3.96 7.5 × 10−5 
2DS3 3 (6.8) 83 (33.9) 0.14 (0.04-0.46) −3.22 .001 
2DS4* 21 (46.7) 139 (56.7) 0.67 (0.35-1.26) −1.24 .21 
2DS5 7 (15.6) 104 (42.4) 0.25 (0.11-0.58) −3.22 .001 
3DS1 9 (20.0) 101 (41.2) 0.36 (0.16-0.77) −2.61 .009 
GenePatients (n = 45), n (%)Control subjects (n = 245), n (%)OR (95% CI)zP
2DS1 5 (11.1) 102 (41.6) 0.18 (0.07-0.46) −3.54 4.0 × 10−4 
2DS2 10 (22.2) 138 (56.3) 0.22 (0.10-0.47) −3.96 7.5 × 10−5 
2DS3 3 (6.8) 83 (33.9) 0.14 (0.04-0.46) −3.22 .001 
2DS4* 21 (46.7) 139 (56.7) 0.67 (0.35-1.26) −1.24 .21 
2DS5 7 (15.6) 104 (42.4) 0.25 (0.11-0.58) −3.22 .001 
3DS1 9 (20.0) 101 (41.2) 0.36 (0.16-0.77) −2.61 .009 

The prefix KIR is not shown with the gene names.

OR indicates odds ratio; and CI, confidence interval.

*

KIR2DS4 was considered absent when the PCR amplified only the 22-bp deleted amplicon. It was considered present when the nonmutant amplicon was observed on the gel with or without the mutant band.

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