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. Author manuscript; available in PMC: 2008 Aug 15.
Published in final edited form as: Clin Cancer Res. 2008 Feb 15;14(4):1090–1095. doi: 10.1158/1078-0432.CCR-07-1195

Table 3.

Cox regression analysis of multi-SNP haplotype–tagged SNPs and ovarian cancer survival

Gene Tagging SNPs Haplotype* Tagged SNPs Missing data Haplotype frequency HR (95% CI) P
CDK6 rs4729049, rs992519 11 rs2374594, rs6975474, rs2374589, rs10246604 2 0.068 1.00 (0.75-1.32) 1.0
rs3217862, rs3217820 00 rs3217827 rs3217881 3 0.48 1.00 (0.88-1.14) 1.0
rs3217869, rs3217852 00 rs3217830 rs3217896 2 0.37 1.00 (0.87-1.15) 1.0
CCND2 rs3217926, rs3217925, rs3217916 000 rs3217907 7 0.35 1.00 (0.87-1.15) 1.0
rs3217926, rs3217936 00 rs4625554 5 0.30 1.00 (0.86-1.19) 1.0
*

0 represents common allele of the tagging SNP in the haplotype; 1 represents rare allele of the tagging SNP in the haplotype.

Number of subjects missing 50% or more of the SNP data for each haplotype.