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. Author manuscript; available in PMC: 2013 Oct 1.
Published in final edited form as: Birth Defects Res A Clin Mol Teratol. 2012 Sep 13;94(10):762–769. doi: 10.1002/bdra.23065

Table 5.

TDT results on SOD2 SNPs association with MM among all patients

Gene SNP A1 A2 T U OR CHISQ P EMP-P
SOD2 rs5746136 A G 104 122 0.8525 1.4340 0.2312 0.2311
SOD2 rs2758331 A C 119 106 1.1230 0.7511 0.3861 0.4147
SOD2 rs5746129 T C 0 2 0.0000 2.0000 0.1573 0.5018
SOD2 rs2855116 T G 108 121 0.8926 0.7380 0.3903 0.4289
SOD2 rs2070994 T A 137 152 0.9013 0.7785 0.3776 0.3915
SOD2 rs2758339 A C 144 152 0.9474 0.2162 0.6419 0.6812
SOD2 rs5746105 C T 92 124 0.7419 4.7410 0.0295 0.0330
SOD2 rs4987023 A G 0 1 0.0000 1.0000 0.3173 1.0000
SOD2 rs5746097 T A 0 3 0.0000 3.0000 0.0833 0.2515
SOD2 rs1799725 T C 20 33 0.6061 3.1890 0.0742 0.0925

Notes: A1 – rare allele, A2 – common allele, T – number of A1 Transmitted, U – number of A1 not transmitted, OR – Odds Ratio, CHISQ – chi square, p-value – PLINK TDT probability, EMP-p – p-value from empirical probability test by permutation. Significant SNP is bolded.