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Table 3 Estimated haplotype frequencies of two SNPs (C23356T and A33065G), estimated log odds ratios and their standard errors for all common haplotypes formed by identified SNPs

From: A systematic search for SNPs/haplotypes associated with disease phenotypes using a haplotype-based stepwise procedure

Haplotype

Control Freq.

Case Freq.

Coef.

Odds Ratio

95% CI

Z-Score

P-value

 

Discovery Cohort (363 patients)

TG

0.33

0.21

 

1.00

(reference)

  

CA

0.39

0.42

0.42

1.52

(1.05, 2.21)

2.21

0.027

CG

0.21

0.23

0.56

1.75

(1.12, 2.72)

2.46

0.014

TA

0.07

0.15

1.21

3.36

(1.77, 6.37)

3.71

0.000

 

Validation Cohort (209 patients)

TG

0.34

0.20

 

1.00

(reference)

  

CA

0.40

0.49

0.68

1.98

(1.19, 3.27)

2.65

0.008

CG

0.18

0.23

0.75

2.11

(0.99, 4.50)

1.94

0.053

TA

0.09

0.09

0.63

1.87

(0.67, 5.23)

1.20

0.230