Table 3.

Genotyping Distribution of the Studied Variables

SNPs	Genotype /Allele	Control	Cases	aP. value	OR	95% C.I	bP. value
		N=50	N=150
rs9642880	GG	27 (54.0%)	90 (60.0%)	0.2	1(reference)
	GT	15 (30.0%)	9 (6.0%)	0.001**	0.18	0.071 - 0.457	0.001**
	TT	8 (16.0%)	51 (34.0%)	0.01*	1.912	0.809 - 4.522	0.03*
	G Allele	69 (0.690)	189 (0.630)	0.3	1 (reference)
	T Allele	31 (0.310)	111 (0.370)		1.307	0.805 - 2.122	0.3
rs710521	AA	6 (12.0%)	30 (20.0%)	0.06	1 (reference)
	AG	17 (34.0%)	69 (46.0%)	0.02*	1.812	0.291 - 3.262	0.04*
	GG	27 (54.0%)	51 (34.0%)	0.001**	0.378	0.140 - 1.020	0.04*
	A Allele	29 (0.290)	129 (0.430)	0.01*	1.847	1.133 - 3.011	0.01*
	G Allele	71 (0.710)	171 (0.570)		1 (reference)

Genotype /Allele are represented as F (%) frequency and percent; the data were analyzed by X² test; * P. value <0.05 is significant, ** P. value <0.01 is highly significant; OR, Odds Ratio; CI, Confidence Interval; *P value ≤ 0.05 significant; **P value ≤ 0.01 highly significant; ^aP. Value is depending on the X² test, while ^bP. Value is depending onLogistic Regression analysis.