Table 2.

Genotypic and allelic frequencies and the risk of CAD and IS

Genotype or allele	Control (%)	CAD (%)	IS (%)	CAD		IS
	n = 539	n = 525	n = 540	OR (95 % CI)	P	OR (95 % CI)	P
rs2902940
GG	74(13.7)	47(9.0)	47(8.7)	1		1
GA	225(41.8)	220(41.9)	242(44.8)	1.48(0.97–2.26)	0.071	1.76(1.14–2.71)	0.011
AA	240(44.5)	258(49.1)	251(46.5)	1.63(1.07–2.48)	0.023	1.69(1.09–2.61)	0.017
P		0.038	0.032
G	373(34.6)	314(29.9)	336(31.1)	1
A	705(65.4)	736(70.1)	744(68.9)	1.22(1.01–1.48)	0.036	1.18(0.98–1.41)	0.078
P		0.021	0.084
HWE(P)	0.071	0.992	0.290
GG	74(13.7)	47(9.0)	47(8.7)	1		1
GA + AA	465(86.3)	478(91.0)	493(91.3)	1.56(1.04–2.32)	0.030	1.72(1.14–2.60)	0.010
P		0.014	0.009
AA	243(45.1)	258(49.1)	251(46.5)	1		1
GA + GG	296(54.9)	267(50.9)	289(53.5)	0.85(0.66–1.09)	0.208	0.93(0.72–1.20)	0.559
P		0.185	0.645
rs6102059
CC	121(22.4)	123(23.4)	108(20.0)	1		1
CT	249(46.2)	261(49.7)	280(51.9)	1.01(0.73–1.39)	0.958	1.19(0.85–1.66)	0.303
TT	169(31.4)	141(26.9)	152(28.1)	0.78(0.55–1.11)	0.170	0.93(0.64–1.33)	0.676
P		0.267	0.178
C	491(44.5)	507(48.3)	496(45.9)
T	587(54.5)	543(51.7)	584(54.1)	0.90(0.76–1.07)	0.233	0.99(0.83–1.17)	0.891
P		0.206	0.860
HWE(P)	0.111	0.917	0.307
CC	129(23.9)	123(23.4)	108(20.0)	1		1
CT + TT	410(76.1)	402(76.6)	432(80.0)	0.96(0.71–1.28)	0.764	1.13(0.83–1.54)	0.443
P		0.847	0.119
TT	169(31.4)	141(26.9)	152(28.1)	1		1
CT + CC	370(68.6)	384(73.1)	388(71.9)	1.29(0.98–1.69)	0.074	1.22(0.93–1.61)	0.155
P		0.107	0.249

HWE Hardy-Weinberg equilibrium, CAD coronary artery disease, IS ischemic stroke