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Table 3 Genotype and allele distributions in patients with CAD and control subjects (Han Chinese)

From: The association of cholesterol absorption gene Numb polymorphism with Coronary Artery Disease among Han Chinese and Uighur Chinese in Xinjiang, China

    

Total

Male

Female

    

CAD n (%)

Control n (%)

P value

CAD n (%)

Control n (%)

P value

CAD n (%)

Control n (%)

P value

rs12435797

Genotype

 

T/T

173(45.6)

185(43.6)

0.378

125(47.2)

94(43.5)

0.436

48(42.1)

91(43.8)

0.924

(SNP1)

  

G/G

38(10.1)

56(13.2)

 

22(8.3)

25(11.6)

 

16(14.0)

31(14.9)

 
 

G/T

168(44.3)

183(43.2)

 

118(44.5)

97(44.9)

 

50(43.9)

86(41.3)

 
  

Dominant model

TT

173(45.6)

185(43.6)

0.570

125(47.2)

94(43.5)

0.462

48(42.1)

91(43.8)

0.815

   

GT + GG

206(54.4)

239(56.4)

 

140(52.8)

122(56.5)

 

66(57.9)

117(56.2)

 
  

Recessive model

GG

38(10.1)

56(13.2)

0.187

22(8.3)

25(11.6)

0.280

16(14.0)

31(14.9)

0.871

   

GT + TT

341(89.9)

368(86.8)

 

243(91.7)

191(88.4)

 

98(86.0)

177(85.1)

 
  

Additive model

GT

168(44.3)

183(43.20)

0.776

118(44.5)

97(44.9)

1

50(43.9)

86(41.3)

0.724

   

TT + GG

211(55.7)

241(56.80)

 

147(55.5)

119(55.1)

 

64(56.1)

122(58.7)

 
 

Allele

 

T

514(67.75)

553(65.20)

0.290

368(69.45)

285(65.95)

0.267

146(64.05)

268(64.45)

0.932

   

G

244(32.25)

295(34.80)

 

162(30.55)

147(34.05)

 

82(35.95)

148(35.55)

 

rs2108552

Genotype

 

C/C

112(29.2)

88(20.5)

0.013*

79(29.3)

36(16.4)

0.003*

33(28.9)

52(24.8)

0.724

(SNP2)

  

G/G

85(22.1)

116(27.1)

 

58(21.5)

62(28.3)

 

27(23.7)

54(25.7)

 
   

C/G

187(48.7)

225(52.4)

 

133(49.2)

121(55.3)

 

54(47.4)

104(49.5)

 
  

Dominant model

CC

112(29.2)

88(20.5)

0.004*

79(29.3)

36(16.4)

0.001*

33(28.9)

52(24.8)

0.430

   

CG + GG

272(70.8)

341(79.5)

 

191(70.7)

183(83.6)

 

81(71.1)

158(75.2)

 
  

Recessive model

GG

85(22.1)

116(27.1)

0.122

58(21.5)

62(28.3)

0.091

27(23.7)

54(25.7)

0.788

   

CG + CC

299(77.9)

313(72.9)

 

212(78.5)

157(71.7)

 

87(76.3)

156(74.3)

 
  

Additive model

CG

187(48.7)

225(52.4)

0.293

133(49.2)

121(55.3)

0.203

54(47.4)

104(49.5)

0.728

   

CC + GG

197(51.3)

204(47.6)

 

137(50.7)

98(44.7)

 

60(52.6)

106(50.5)

 
 

Allele

 

C

411(53.55)

401(46.7)

0.007*

291(53.9)

193(44.05)

0.003*

120(52.6)

208(49.55)

0.460

   

G

357(46.45)

457(53.3)

 

249(46.1)

245(55.95)

 

108(47.4)

212(50.45)

 

rs1019075

Genotype

 

C/C

21(5.5)

24(5.6)

0.041*

12(4.5)

9(4.1)

0.060

9(7.9)

15(7.2)

0.351

(SNP3)

  

T/T

257(67.3)

252(59.0)

 

179(66.8)

124(56.9)

 

78(68.4)

128(61.2)

 
   

C/T

104(27.2)

151(35.4)

 

77(28.7)

83(39.0)

 

27(23.7)

66(31.6)

 
  

Dominant model

CC

21(5.5)

24(5.6)

1

12(4.5)

9(4.1)

1

9(7.9)

15(7.2)

0.827

   

CT + TT

361(94.5)

403(94.4)

 

256(95.5)

209(95.9)

 

105(92.1)

194(92.8)

 
  

Recessive model

TT

257(67.3)

252(59.0)

0.016*

179(66.8)

124(56.9)

0.030*

78(68.4)

128(61.2)

0.226

   

CT + CC

125(32.7)

175(41.0)

 

89(33.2)

94(43.1)

 

36(31.6)

81(38.8)

 
  

Additive model

CT

104(27.2)

151(35.4)

0.015*

77(28.7)

83(39.0)

0.020*

27(23.7)

66(31.6)

0.158

   

CC + TT

278(72.9)

276(64.6)

 

191(71.3)

133(61.0)

 

87(76.3)

143(68.4)

 
 

Allele

 

C

146(19.1)

199(23.3)

0.045*

101(18.85)

101(23.6)

0.081*

45(19.75)

96(23.0)

0.371

   

T

618(80.9)

655(76.7)

 

435(81.15)

341(76.4)

 

183(80.25)

322(77.0)

 

rs17781919

Genotype

 

C/C

384(100.0)

429(99.89)

1

270(100.0)

220(100.0)

1

114(100.0)

209(99.5)

1

(SNP4)

  

C/T

0(0.0)

1(0.2)

 

0(0.0)

0(0.0)

 

0(0.0)

1(0.5)

 
 

Allele

 

C

768(100.0)

859(99.9)

1

540(100.0)

440(100.0)

1

228(100.0)

419(99.8)

1

   

T

0(0.0)

1(0.1)

 

0(0.0)

0(0.0)

 

0(0.0)

1(0.2)

 
  1. CAD coronary artery disease. The P value of genotype was calculated by Fisher’s exact test. * P <0.05