Table 7.

Association of omentin rs2274908 G>A gene variation with the susceptibility to CAD patients.

Genotypes	Healthy Controls	CAD Cases	OR (95% CI)	Risk Ratio (RR)	P-Value
	(N = 100)	(N = 100)
Codominant
ITLN1-GG	16	21	1 (ref.)	1 (ref.)
ITLN1-GA	84	78	0.70 (0.344 to 1.45)	0.83 (0.56 to 1.24)	0.34
ITLN1-AA	0	1	2.30 (0.08 to 60.23)	1.73 (0.15 to 19.68)	0.61
Dominant
ITLN1-GG	16	21	1 (ref.)	1 (ref.)
ITLN1-(GA + AA)	84	79	0.71 (0.34 to 1.47)	0.83 (0.56 to 1.24)	0.36
Recessive
ITLN1-(GG + GA)	100	99	1 (ref.)	1 (ref.)
ITLN1-AA	0	1	3.03 (0.12 to 75.28)	2.0 (0.181 to 22.255)	0.49
Allele
ITLN1-G	116	120	1 (ref.)	1 (ref.)
ITLN1-A	84	80	0.92 (0.61 to 1.37)	0.95 (0.78 to 1.16)	0.68