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. 2014 Oct 24;15(11):19406–19416. doi: 10.3390/ijms151119406

Table 1.

Allelic and genotypic frequencies of the single-nucleotide polymorphism (SNP) association analyze.

Makers Allele Frequency (%) p-Value a OR b (95% CI) Genotype Frequency (%) p-Value a HWE p-Value Models OR b (95% CI) p-Value a
SNPs ID
SNP1 rs6943555 A T 0.097 AA AT TT 0.001 0.496
SCZ 33.0 77.0 1.191 7.8 50.5 41.7 Dominant 1.363 (0.848–2.191) 0.001
CTR 29.3 70.7 (0.969–1.463) 10.4 37.9 51.7 Recessive 0.734 (0.456–1.180) 0.201
Addictive 1.197 (0.971–1.475) 0.093
SNP2 rs7459368 G A 0.720 GG AG AA 0.809 0.954
SCZ 17.4 82.6 1.047 2.7 29.5 67.8 Dominant 1.117 (0.495–2.523) 0.809
CTR 16.8 83.2 (0.813–1.349) 3.0 27.6 69.4 Recessive 0.895 (0.396–2.021) 0.789
Addictive 1.048 (0.813–1.351) 0.719
SNP3 rs9886351 G A 0.681 GG AG AA 0.803 0.114
SCZ 27.4 72.6 0.956 8.3 38.3 53.4 Dominant 1.028 (0.632–1.672) 0.803
CTR 26.6 73.4 (0.771–1.185) 8.5 36.1 55.4 Recessive 1.067 (0.662–1.719) 0.789
Addictive 1.030 (0.825–1.286) 0.794

SCZ: schizophrenia; CTR: control; OR: odds ratio; CI: confidence interval; SNP1: rs6943555; SNP2: rS7459368; SNP3: rS9886351; HWE: Hardy–Weinberg equilibrium. Significant p-values and HWE p-values were shown in bold font. a: p-values were based on normal chi-square statistics; b: OR refers to the risk allele odds ratio for both the cases and controls.