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Table 7 Haplotype analysis in patients with CAD and control subjects (Uighur Chinese)

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

   

Total(n = 857)

Male(n = 582)

Female(n = 275)

   

Case(freq)

Control(freq)

χ2

P value

Odds ratio(95 % CI)

Case(freq)

Control(freq)

χ2

P value

Odds ratio(95 % CI)

Case(freq)

Control(freq)

χ2

P value

Odds ratio(95 % CI)

1

0100

G G C C

305.11(0.303)

238.23(0.336)

2.284

0.131

0.853(0.693–1.049)

224.57(0.307)

133.44(0.342)

1.548

0.214

0.846(0.650–1.101)

80.43(0.294)

105.09(0.330)

1.082

0.298

0.830(0.584–1.179)

2

0110

G G T C

218.04(0.217)

148.10(0.209)

0.116

0.734

1.042(0.823–1.319)

154.87(0.212)

80.23(0.206)

0.045

0.833

1.033(0.762–1.400)

63.54(0.232)

67.89(0.213)

0.235

0.628

1.101(0.746–1.625)

3

1010

T C T C

333.07(0.331)

215.98(0.305)

1.021

0.273

1.123(0.912–1.383)

245.28(0.335)

118.66(0.304)

1.063

0.302

1.150(0.881–1.501)

87.67(0.320)

96.81(0.304)

0.115

0.735

1.062(0.749–1.508)

4

1100

T G C C

39.770.040)

21.50(0.030)

0.987

0.321

1.310(0.768–2.234)

25.32(0.035)

11.14(0.029)

0.287

0.592

1.216(0.594–2.487)

14.73(0.054)

10.38(0.033)

1.559

0.212

1.669(0.741–3.758)

5

1110

T G T C

88.09(0.088)

66.38(0.094)

0.215

0.643

0.924(0.661–1.291)

64.24(0.088)

36.19(0.093)

0.087

0.769

0.938(0.611–1.439)

23.46(0.086)

30.34(0.095)

0.199

0.656

0.879(0.500–1.548)

  1. CAD coronary artery disease, SNP single nucleotide polymorphism. The p value of haplotype was calculated by Fisher’s exact test. * P < 0.05.
  2. Haplotypes with frequencies >0.03 were estimated using SHEsis software; 0 represents major allele and 1 represents minor allele “0100” refers respectively the major allele of the SNP1,minor allele of the SNP2,major allele of the SNP3,major allele of the SNP4