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Table 6 Haplotype analysis 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(n = 817)

Male(n = 490)

Female(n = 327)

   

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

134.72(0.176)

183.90(0.209)

3.375

0.066

0.793(0.619–1.016)

91.93(0.173)

94.94(0.214)

2.500

0.114

0.773(0.561–1.064)

42.77(0.184)

88.94(0.204)

0.449

0.503

0.871(0.580–1.306)

2

0110

G G T C

93.07(0.122)

142.93(0.163)

6.157

0.013*

0.701(0.529–0.929)

64.86(0.122)

82.06(0.185)

7.302

0.007*

0.616(0.432–0.877)

28.23(0.122)

60.60(0.139)

0.457

0.498

0.848(0.526–1.368)

3

1010

T C T C

407.79(0.534)

400.78(0.456)

8.271

0.004*

1.334(1.096–1.624)

285.79(0.537)

196.99(0.444)

9.138

0.002*

1.482(1.148–1.912)

122.00(0.526)

204.52(0.469)

1.626

0.202

1.231(0.894–1.694)

4

1100

T G C C

11.27(0.015)

23.24(0.026)

0

0

0

9.06(0.017)

6.06(0.014)

0

0

0

2.23(0.010)

17.20(0.039)

4.853

0.028*

0.234(0.057–0.952)

5

1110

T G T C

115.93(0.152)

123.93(0.141)

0.293

0.625

1.071(0.814–1.409)

79.14(0.149)

63.94(0.444)

0.061

0.805

1.046(0.732–1.495)

36.77(0.158)

60.27(0.138)

0.428

0.513

1.160(0.743–1.811)

  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