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Table 5 Allele and genotype frequencies of SNPs in CP patients with neonatal encephalopathy and controls

From: Association of NOS1 gene polymorphisms with cerebral palsy in a Han Chinese population: a case-control study

Group Allele frequency P OR (95% CI) Genotype frequency P
rs3782219 C T    C/C C/T T/T  
Case 300 (0.575) 222 (0.425) 0.185 0.869 82 (0.314) 136 (0.521) 43 (0.165) 0.289
Control 774 (0.608) 498 (0.392)   (0.707~ 1.069) 235 (0.369) 304 (0.478) 97 (0.153)  
rs2293054 A G    A/A A/G G/G  
Case 122 (0.234) 400 (0.766) 0.100 1.228 15 (0.057) 92 (0.352) 154 (0.590) 0.256
Control 253 (0.199) 1019 (0.801)   (0.961~ 1.560) 26 (0.041) 201 (0.316) 409 (0.643)  
rs10774909 C G    C/C C/G G/G  
Case 343 (0.657) 179 (0.343) 0.364 0.905 98 (0.375) 147 (0.563) 16 (0.061) 0.001 a
Control 864 (0.679) 408 (0.321)   (0.729~ 1.123) 294 (0.462) 276 (0.434) 66 (0.104)  
rs3741475 A G    A/A A/G G/G  
Case 145 (0.278) 377 (0.722) 0.675 1.050 10 (0.038) 125 (0.479) 126 (0.483) 0.003 b
Control 341 (0.268) 931 (0.732)   (0.836~ 1.319) 52 (0.082) 237 (0.373) 347 (0.546)  
rs2682826 A G    A/A A/G G/G  
Case 145 (0.278) 377 (0.722) 0.531 1.076 9 (0.034) 127 (0.487) 125 (0.479) 0.0005 c
Control 335 (0.263) 937 (0.737)   (0.856~ 1.352) 52 (0.082) 231 (0.363) 353 (0.555)  
  1. aAfter the SNPSpD correction, p = 0.004; bAfter the SNPSpD correction, p = 0.012; cAfter the SNPSpD correction, p = 0.002