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

Table 5.

Genotypic and allelic distribution of the NLRP3 gene between all patients (n = 163) and controls (n = 201).

SNP Genotype/allele Case (%) Control (%) p valuea(χ2) OR (95% CI) p valueb
rs4612666 CC 44 (27.0) 59 (29.4) 0.220 (3.026) 1.00 Referent
CT 90 (55.2) 94 (46.8) 0.779 (0.479–1.266) 0.313
TT 29 (17.8) 48 (23.9) 1.234 (0.675–2.258) 0.495
CT + TT 119 (73.0) 142 (70.6) 0.584 (0.300) 0.890 (0.562–1.410) 0.619
C 178 (54.6) 212 (52.7) 0.616 (0.252) 1.00 Referent
T 148 (45.4) 190 (47.3) 1.078 (0.804–1.445) 0.616

rs10754558 CC 50 (30.7) 76 (37.8) 0.313 (2.322) 1.00 Referent
CG 84 (51.5) 89 (44.3) 0.697 (0.438–1.110) 0.128
GG 29 (17.8) 36 (17.9) 0.817 (0.446–1.496) 0.512
CG + GG 113 (69.3) 125 (62.2) 0.155 (2.025) 0.728 (0.470–1.128) 0.155
C 184 (56.4) 241 (60.0) 0.340 (0.912) 1.00 Referent
G 142 (43.6) 161 (40.0) 0.866 (0.644–1.164) 0.340

rs2027432 CC 151 (92.6) 180 (89.5) 0.549 (1.200) 1.00 Referent
CT 11 (6.8) 20 (10.0) 1.525 (0.708–3.284) 0.281
TT 1 (0.6) 1 (0.5) 0.839 (0.052–13.525) 0.901
CT + TT 12 (7.4) 21 (10.5) 0.308 (1.040) 1.468 (0.699–3.082) 0.310
C 313 (96.0) 380 (94.5) 0.352 (0.867) 1.00 Referent
T 13 (4.0) 22 (5.5) 1.394 (0.691–2.812) 0.354

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.