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. 2012 Apr 24;14(2):R85. doi: 10.1186/ar3809

Table 2.

Association of CD226 haplotype block in the Fib+ subset of systemic sclerosis patients.

rs763361 rs34794968 rs727088 Subgroup MAF (%) P MH P Bonf OR [CI 95%] P BD
Fib+ 0.40
T A G CTRL 0.41 0.59 NS 0.97 [0.86-1.08] 0.45
Fib- 0.41 0.76 NS 0.98 [0.86-1.11] 0.77

Fib+ 0.10
T C G CTRL 0.08 1.59E-02 3.18E-02 1.27 [1.05-1.54] 0.48
Fib- 0.08 0.069 NS 1.24 [0.99-1.56] 0.51

Fib+ 0.50
C C A CTRL 0.51 0.44 NS 0.96 [0.86-1.07] 0.71
Fib- 0.51 0.50 NS 0.95 [0.84-1.09] 0.44

For the haplotype-specific analyses, the odds ratio (OR) with 95% confidence interval (95% CI) was determined for each allele variant in the haplotype tested against all of the others pooled together using the Mantel-Haenszel test under fixed effects model, considering no single reference haplotype. CTRL, healthy controls; Fib-, lung fibrosis negative SSc patients; Fib+, lung fibrosis positive SSc patients; MAF, minor allele frequency; PBonf, corrected P-value using Bonferroni multiple test correction.