Skip to main content
. 2015 Jun 19;10(6):e0128586. doi: 10.1371/journal.pone.0128586

Table 4. Haplotypic associations with PD.

A. US series (895 patients, 976 controls)*
Haplotype (rs56031549, del6, ins3, del21, rs2102808, rs4496303) MAF in cases (%) MAF in controls (%) OR P P corr
111112 0.96 1.25 0.68 (0.34–1.34) 0.26 1
121221 5.3 4.62 1.17 (0.86–1.58) 0.31 1
121121 8.59 6.71 1.4 (1.09–1.8) 0.009 0.06
112111 2.64 1.74 1.63 (1.02–2.61) 0.04 0.25
122111 12.93 14.42 0.86 (0.71–1.04) 0.11 0.66
111111 69.58 71.27 0.91 (0.78–1.05) 0.18 1
B. Irish series (368 patients, 368 controls)*
Haplotype (rs56031549, del6, ins3, del21, rs2102808, rs4496303) MAF in cases (%) MAF in controls (%) OR P P corr
111112 1.19 0.68 1.86 (0.55–6.28) 0.32 1
121221 6.96 5.69 1.18 (0.77–1.81) 0.45 1
121121 6.99 5.58 1.23 (0.81–1.88) 0.34 1
112111 2.67 2.74 0.91 (0.47–1.78) 0.79 1
122111 10.05 10.86 0.92 (0.65–1.32) 0.66 1
111111 69.67 72.07 0.93 (0.73–1.18) 0.54 1
C. Polish series (713 patients, 252 controls)*
Haplotype (rs56031549, del6, ins3, del21, rs2102808, rs4496303) MAF in cases (%) MAF in controls (%) OR P P corr
111112 1.03 1.87 0.46 (0.2–1.09) 0.08 0.46
121221 6.85 7.4 0.97 (0.64–1.46) 0.87 1
121121 7.17 5.11 1.45 (0.9–2.34) 0.13 0.78
112111 2.2 2.22 1.07 (0.55–2.08) 0.84 1
122111 14.97 14.39 1.05 (0.78–1.41) 0.75 1
111111 67.78 69 0.93 (0.74–1.17) 0.53 1
D. Combined series (1976 patients, 1596 controls)*
Haplotype (rs56031549, del6, ins3, del21, rs2102808, rs4496303) MAF in cases (%) MAF in controls (%) OR P P corr
111112 1.03 1.26 0.74 (0.46–1.21) 0.23 1
121221 6.15 5.33 1.1 (0.9–1.35) 0.36 1
121121 7.86 6.27 1.35 (1.11–1.64) 0.003 0.02
112111 2.52 2.1 1.3 (0.93–1.81) 0.12 0.71
122111 13.19 13.66 0.92 (0.8–1.06) 0.27 1
111111 69.24 71.39 0.91 (0.82–1.02) 0.1 0.57

Haplotypes are encoded as 1 for major allele and 2 for minor allele see Table 2 for specific alleles, MAF = minor allele frequency, OR = Odds ratio, CI = confidence interval, P = p-value, P corr = P-value with Bonferroni correction. ORs, 95% CIs, and P-values result from haplotype-based logistic regression analysis.

*Numbers of samples with complete clinical information included in model.