TaqI, FokI, and ApaI Polymorphisms in the Vitamin D Receptor in Behçet’s Disease in Turkish Population

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 (%)	All patients	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
	2.80	0.989
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
	1.511	0.213
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
	0.068	0.074
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 value < 0.05.