Table 6.
Markers in the haplotype block | AS nuclear families (n = 226) | Testing specifically for affected women | Testing specifically for affected men |
Additive model | |||
rs26307, rs27356 | [C,C]; 0.78; 39; 0.04 | NS | [C,C]; 0.79; 24; 0.014 |
3088132, rs153929 | NS | NS | NS |
rs28006, rs25957 | NS | [T,G]; 0.25; 19; 0.007 | NS |
ANKH-OR, D5S1991 | [1,2]; 0.43; 57; 0.013 | NS | NS |
Recessive/dominant model | |||
rs26307, rs27356 | [C,C]; 0.78; 40; 0.02 | NS | [C,C]; 0.79; 25; 0.004* |
3088132, rs153929 | [G,A]; 0.70; 32; 0.02 | NS | NS |
rs28006, rs25957 | NS | [C,C]; 0.71; 18; 0.004* | NS |
ANKH-OR, D5S1991 | NS | NS | NS |
Data are expressed as [allele]; allele frequency; number of informative families; P value.
*Significant P value after Bonferroni correction. (Because eight tests [four haplotypes and two models] were carried out in the haplotype-based association testing [HBAT]-e analyses, P < 0.00625 [0.05/8] is considered statistically significant.) AS, ankylosing spondylitis; NS, not significant.