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. 2016 Sep 1;2016:7475080. doi: 10.1155/2016/7475080

Table 3.

Distribution of genotype and alleles frequencies of VDR SNPs in all patients (Behçet's disease and neuro-Behçet's disease) and control subjects.

  Controls n (%) All patients p value
ApaI genotype      
 AC 10 (33.3) 24 (42.9) 0.389
 AA 13 (43.3) 13 (23.2) 0.053
 CC 7 (23.4) 19 (33.9) 0.308
 HWE      
   χ 2 2.80 0.989  
   p value 0.0942 0.319  

ApaI alleles      
 A 36 (60) 50 (44.6)  
 C 24 (40) 62 (55.4) 0.05

TaqI genotype      
 CT 11 (36.7) 24 (41.4) 0.669
 TT 13 (43.3) 27 (46.6) 0.774
 CC 6 (20) 7 (12.1) 0.320
 HWE      
   χ 2 1.511 0.213  
   p value 0.218 0.643  

TaqI alleles      
 C 23 (38.3) 38 (32.8)  
 T 37 (61.7) 78 (67.2) 0.46

FokI genotype      
 CT 12 (40) 22 (37.9) 0.85
 TT 15 (50) 33 (56.9) 0.538
 CC 3 (10) 3 (5.2) 0.394
 HWE      
   χ 2 0.068 0.074  
   p value 0.794 0.785  

FokI alleles      
 T 42 (70) 88 (75.8)  
 C 18 (30) 28 (24.2) 0.40

Differences were considered statistically significant at a p value < 0.05.