Table 2.

Comparison of rs1799724 and rs266085 genotype and allele frequencies in cervical cancer cases and controls

SNP	Case (%)	Control (%)			Model
	N=348	N=351	OR (95 CI)	P-value	Model	OR (95% CI)	P-value
rs1799724
Genotype
CC/CC	215 (61.8)	301 (85.8)	1.00 (reference)		Dom	3.72 (2.57-5.38)	0.000
TC/TC	87 (25.0)	44 (12.5)	2.77 (1.85-4.14)	0.000	Rec	8.76 (3.69-20.79)	0.000
TT/TT	46 (13.2)	6 (1.7)	10.73 (4.50-25.58)	0.000	Add	3.00 (2.22-4.05)	<.0001
Alleles
CC Alleles	74.3	92.0	1.00 (reference)	0.000
TT Alleles	25.7	8.0	3.99 (2.90-5.51)
rs266085
Genotype
CC/CC	73 (21.0)	66 (18.8)	1.00 (reference)		Dom	0.87 (0.60-1.27)	0.472
TC/TC	141 (40.5)	217 (61.8)	1.70 (1.15-2.53)	0.008	Rec	2.61 (1.85-3.67)	0.000
TT/TT	134 (38.5)	68 (19.4)	1.78 (1.14-2.77)	0.010	Add	1.43 (1.15-1.77)	0.001
Alleles
CC Alleles	41.2	49.7	1.00 (reference)	0.000
TT Alleles	58.8	50.3	1.41 (1.14-1.74)

OR, odds ratios under a recessive model (OR=1 indicates no association between the gene and the disease; OR>1 indicates risk factor for the disease; OR<1 indicates protective factor against the disease); CI, confidence interval; Dom, dominant model; Rec, recessive model; Add, additive model.