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Table 4 Genotyping and allele distributions in control subjects and patients with CAD in the Uygur population

From: Association of Egr 3 genetic polymorphisms and coronary artery disease in the Uygur and Han of China

 

Total

Men

Women

Variants

CAD patients

Control subjects

P value

CAD patients

Control subjects

P value

CAD patients

Control subjects

P value

rs1996147

         

Genotyping

         

AA

109(36.5%)

75(24.7%)

 

77(38.9%)

49(25.0%)

 

32(31.7%)

26(24.3%)

 

AG

142(47.5%)

156(51.5%)

 

90(45.5%)

98(50.0%)

 

52(51.5%)

58(54.2%)

 

GG

48(16.0%)

72(23.8%)

0.003*

31(15.6%)

49(25.0%)

0.005*

17(16.8%)

23(21.5%)

0.433

Dominant model

         

GG

48(16.0%)

72(23.8%)

 

31(15.6%)

49(25.0%)

 

17(16.8%)

23(21.5%)

 

AA + AG

251(84.0%)

231(76.2%)

0.018*

167(84.4%)

147(75.0%)

0.021*

84(83.2%)

84(78.5%)

0.394

Recessive model

         

AA

109(36.5%)

75(24.7%)

 

77(38.9%)

49(25.0%)

 

32(31.7%)

26(24.3%)

 

GG + AG

190(63.5%)

228(75.3%)

0.002*

121(61.1%)

147(75.0%)

0.003*

69(68.3%)

81(75.7%)

0.235

Additive model

         

AG

142(47.5%)

156(51.5%)

 

90(45.5%)

98(50.0%)

 

52(51.5%)

58(54.2%)

 

AA + GG

157(52.5%)

147(48.5%)

0.327

108(54.5%)

98(50.0%)

0.366

49(48.5%)

49(45.8%)

0.694

Allele

         

A

360(60.2%)

306(50.5%)

 

244(61.6%)

196(50.0%)

 

116(57.4%)

110(51.4%)

 

G

238(39.8%)

300(49.5%)

0.001*

152(38.4%)

196(50.0%)

0.001*

86(42.6%)

104(48.6%)

0.218

rs1008949

         

Genotyping

         

CC

118(39.5%)

104(34.3%)

 

77(38.9%)

66(33.7%)

 

41(40.6%)

38(35.5%)

 

CT

136(45.5%)

152(50.2%)

 

95(48.0%)

98(50.0%)

 

41(40.6%)

54(50.5%)

 

TT

45(15.0%)

47(15.5%)

0.409

26(13.1%)

32(16.3%)

0.472

19(18.8%)

15(14.0%)

0.334

Dominant model

         

CC

118(39.5%)

104(34.3%)

 

77(38.9%)

66(33.7%)

 

41(40.6%)

38(35.5%)

 

TT + CT

181(60.5%)

199(65.7%)

0.191

121(61.1%)

130(66.3%)

0.282

60(59.4%)

69(64.5%)

0.451

Recessive model

         

TT

45(15.0%)

47(15.5%)

 

26(13.1%)

32(16.3%)

 

19(18.8%)

15(14.0%)

 

CC + CT

254(85.0%)

256(84.5%)

0.875

172(86.9%)

164(83.7%)

0.371

82(81.2%)

92(86.0%)

0.350

Additive model

         

CT

136(45.5%)

152(50.2%)

 

95(48.0%)

98(50.0%)

 

41(40.6%)

54(50.5%)

 

CC + TT

163(54.5%)

151(49.8%)

0.267

103(52.0%)

98(50.0%)

0.688

60(59.4%)

53(49.5%)

0.153

Allele

         

C

372(62.2%)

360(59.4%)

 

249(62.9%)

230(58.7%)

 

123(60.9%)

130(60.7%)

 

T

226(37.8%)

246(40.6%)

0.319

147(37.1%)

162(41.3%)

0.227

79(39.1%)

84(39.3%)

0.976

  1. CAD, coronary artery disease; SNP, single-nucleotide polymorphism; *P < 0.05.