Table 4

Association between activating KIR genes and risk for T-ALL in white

GenePatients (n = 30), n (%)Control subjects (n = 245), n (%)OR (95% CI)P
2DS1 6 (20.0) 102 (41.6) 0.35 (0.14-0.89) .027 
2DS2 9 (30.0) 138 (56.3) 0.32 (0.15-0.75) .009 
2DS3 2 (6.8) 83 (33.9) 0.14 (0.03-0.60) .008 
2DS4* 12 (40.0) 139 (56.7) 0.51 (0.23-1.10) .086 
2DS5 8 (26.7) 104 (42.4) 0.49 (0.21-1.15) .100 
3DS1 8 (26.7) 101 (41.2) 0.52 (0.22-1.21) .130 
GenePatients (n = 30), n (%)Control subjects (n = 245), n (%)OR (95% CI)P
2DS1 6 (20.0) 102 (41.6) 0.35 (0.14-0.89) .027 
2DS2 9 (30.0) 138 (56.3) 0.32 (0.15-0.75) .009 
2DS3 2 (6.8) 83 (33.9) 0.14 (0.03-0.60) .008 
2DS4* 12 (40.0) 139 (56.7) 0.51 (0.23-1.10) .086 
2DS5 8 (26.7) 104 (42.4) 0.49 (0.21-1.15) .100 
3DS1 8 (26.7) 101 (41.2) 0.52 (0.22-1.21) .130 

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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