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. Author manuscript; available in PMC: 2016 Dec 23.
Published in final edited form as: Birth Defects Res A Clin Mol Teratol. 2015 Aug 17;103(10):857–862. doi: 10.1002/bdra.23413

Table 3.

TDT analysis for SNPs in and near FOXF2 gene in 216 Asian and 75 European NSCL/P trios

SNPs Position build 38 Minor allele MAF (%) FAM T NT OR (95%CI) P Value Bonferroni P Value Empiric P Value
Asian
rs3799321 1391817 C 4.1 32 18 16 1.13 (0.57, 2.21) 0.73 1 1
rs1711968 1391873 C 22.4 101 84 41 2.05 (1.41, 2.98) 0.00012 0.00072 0.0016
rs9405473 1392224 T 2.9 21 14 8 1.75 (0.73, 4.17) 0.2 1 0.85
rs732835 1392765 C 26.0 119 92 52 1.77 (1.26, 2.49) 0.00086 0.0043 0.005
rs3823148 1392958 G 2.6 19 13 7 1.86 (0.74, 4.66) 0.18 1 0.75
rs2293783 1394808 C 23.8 114 85 53 1.60 (1.14, 2.26) 0.00645 0.032 0.054

European
rs1711968 1391873 C 45.6 32 17 22 0.77 (0.41, 1.46) 0.42 1 0.98
rs732835 1392765 C 20.7 25 9 20 0.45 (0.20, 0.99) 0.041 0.16 0.063
rs2293783 1394808 C 22.1 27 10 23 0.43 (0.21, 0.91) 0.024 0.1 0.093
rs1737762 1395878 A 25.2 27 20 14 1.43 (0.72, 2.83) 0.3 1 0.95
*

FAM: number of informative families, T: number of transmitted alleles, NT: number of un-transmitted alleles; Empiric P Value: P values for 10,000 permutations in Haploview