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. 2016 Apr 18;2016:8389020. doi: 10.1155/2016/8389020

Table 4.

Distributions of rs2070874, rs2243248, and rs1800925 polymorphisms in CP patients and healthy controls.

SNP Genotype/allele CP patients
N = 440 (%)
Controls
N = 324 (%)
Crude OR (95% CI) P value Adjusted OR (95% CI)a P value
rs2070874 T/T 289 (65.7) 210 (64.8) 1 1
C/T 130 (29.5) 96 (29.6) 0.984 (0.716–1.352) 0.935 1.062 (0.266–4.244) 0.933
C/C 21 (4.8) 18 (5.6) 0.848 (0.441–1.631) 0.619 1.082 (0.215–5.460) 0.924
T 708 (80.5) 516 (79.6) 1 1
C 172 (19.5) 132 (20.4) 0.950 (0.737–1.224) 0.698 1.216 (0.455–3.247) 0.696

rs2243248 T/T 401 (91.1) 261 (80.6) 1 1
G/T 38 (8.6) 57 (17.6) 0.434 (0.280–0.673) 0.001 0.276 (0.237–0.322) 0.002
G/G 1 (2.3) 6 (1.8) 0.108 (0.013–0.906) 0.018 0.109 (0.085–0.140) 0.001
T 840 (95.5) 579 (89.4) 1 1
G 40 (4.5) 69 (10.6) 0.400 (0.267–0.598) 0.001 0.321 (0.290–0.355) 0.001

rs1800925 C/C 330 (75.0) 227 (70.1) 1 1
C/T 96 (21.8) 93 (28.7) 0.710 (0.510–0.989) 0.050 0.826 (0.615–1.109) 0.204
T/T 14 (3.2) 4 (1.2) 2.408 (0.782–7.408) 0.145 2.091 (1.230–3.556) 0.301
C 756 (85.9) 547 (84.4) 1 1
T 124 (14.1) 101 (15.6) 0.888 (0.668–1.181) 0.422 1.005 (0.736–1.371) 0.977

aAdjusted for gender and age.

OR, odds ratio; CI, confidence interval.

Significant difference was accepted at P < 0.05.

Homozygous genotypes were used as reference group.