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. 2016 Sep 29;16:25. doi: 10.1186/s12878-016-0064-6

Table 3.

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

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

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