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Table 3 Frequency of each KIR gene in patients (N = 39) and controls (N = 136)

From: KIR repertory in patients with hematopoietic diseases and healthy family members

 

KIR gene

Patient

Control

p-value

(n = 39)

(n = 136)

 

Framework

KIR2DL4

39 (100 %)

136 (100 %)

1.0000

KIR3DL2

39 (100 %)

136 (100 %)

1.0000

KIR3DL3

39 (100 %)

136 (100 %)

1.0000

KIR3DP1

39 (100 %)

136 (100 %)

1.0000

Haplotype A

KIR2DS4

36 (92 %)

129 (95 %)

0.6936

KIR2DL1

35 (90 %)

130 (96 %)

0.2329

KIR2DL3

36 (92 %)

118 (87 %)

0.4173

KIR3DL1

37 (95 %)

129 (95 %)

1.0000

Haplotype B

KIR2DS1

6 (15 %)

59 (43 %)

0.0013 ( a )

KIR2DS2

12 (31 %)

78 (57 %)

0.0038 ( a )

KIR2DS3

5 (13 %)

45 (33 %)

0.0153 ( a )

KIR2DS5

11 (28 %)

45 (33 %)

0.6976

KIR3DS1

10 (26 %)

53 (39 %)

0.1356

KIR2DL2

9 (23 %)

75 (55 %)

0.0005 ( a )

KIR2DL5

11 (28 %)

72 (53 %)

0.0067 ( a )

Haplotype A/B

KIR2DP1

37 (95 %)

131 (96 %)

0.6465

  1. Genes in bold showed significance for the statistical test (a)