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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 3.

TDT results on SOD1 SNPs association with MM among all patients

CHR SNP A1 A2 T U OR CHISQ P EMP-P
SOD1 rs202446 A C 20 40 0.5000 6.6670 0.0098 0.0133
SOD1 rs202447 T G 6 20 0.3000 7.5380 0.0060 0.0154
SOD1 rs11910115 C A 6 7 0.8571 0.0769 0.7815 1.0000
SOD1 rs4816405 G C 85 122 0.6967 6.6140 0.0101 0.0125
SOD1 rs4998557 A G 77 95 0.8105 1.8840 0.1699 0.1629
SOD1 rs2070424 G A 69 104 0.6635 7.0810 0.0078 0.0071
SOD1 rs1041740 T C 142 163 0.8712 1.4460 0.2292 0.2304

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 SNPs are bolded.