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. 2017 Apr 19;2017:9547902. doi: 10.1155/2017/9547902

Table 6.

Genotypic and allelic distribution of the P2RX7 gene between all patients (n = 163) and controls (n = 201).

SNP Genotype/allele Case (%) Control (%) p valuea(χ2) OR (95% CI) p valueb
rs3751143 TT 94 (57.7) 127 (63.2) 0.451 (1.592) 1.00 Referent
TG 59 (36.2) 66 (32.8) 0.828 (0.533–1.287) 0.401
GG 10 (6.1) 8 (4.0) 0.592 (0.225–1.558) 0.288
GT + GG 69 (42.3) 74 (36.8) 0.284 (1.148) 0.794 (0.520–1.211) 0.284
T 247 (75.8) 320 (79.6) 0.215 (1.537) 1.00 Referent
G 79 (24.2) 82 (20.4) 0.801 (0.564–1.138) 0.215

rs208294 AA 58 (35.6) 69 (34.3) 0.741 (0.599) 1.00 Referent
AG 83 (50.9) 99 (49.3) 1.003 (0.636–1.580) 0.991
GG 22 (13.5) 33 (16.4) 1.261 (0.663–2.397) 0.480
AG + GG 105 (64.4) 132 (65.7) 0.830 (0.062) 1.057 (0.685–1.630) 0.803
A 199 (61.0) 237 (59.0) 0.568 (0.327) 1.00 Referent
G 127 (39.0) 165 (41.0) 1.091 (0.809–1.470) 0.568

CI, confidence interval; OR, odds ratio.

a p value for genotype and allele frequencies in cases and controls using 2-sided χ2 test.

b p values adjusted by age and gender using logistic regression.