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. 2015 Apr 13;10(4):e0123959. doi: 10.1371/journal.pone.0123959

Table 1. Association of rs870142 (T>C), rs16835979 (A>C) and rs6824295 (T>C) polymorphisms with ASD.

SNP Genotype frequency n (%) Allele frequency n (%) OR(95%CI) P P perm P FDR-BH
rs870142 CC TC TT T C
Cases(190) 77(40.5) 83(43.7) 30(15.8) 143(37.6) 237(62.4) 2.826(1.451–5.505) a 0.002 0.003 0.006
Controls(225) 110(48.9) 101(44.9) 14(6.2) 129(28.7) 321(71.3) 1.501(1.122–2.009) b 0.006 0.006 0.018
rs16835979 CC AC AA A C
Cases (190) 79(41.6) 80(42.1) 31(16.3) 142(37.4) 238(62.6) 2.730(1.425–5.228) a 0.002 0.003 0.003
Controls(225) 111(49.3) 99(44.0) 15(6.7) 129(28.7) 321(71.3) 1.485(1.109–1.987) b 0.008 0.009 0.012
rs6824295 CC TC TT T C
Cases (190) 72(40.7) 86(42.2) 32(17.1) 150(39.5) 230(60.5) 2.478(1.328–4.623) a 0.003 0.004 0.003
Controls (225) 98(50.0) 110(42.0) 17(8.0) 144(32.0) 306(68.0) 1.386(1.042–1.844) b 0.025 0.028 0.025

a the value of OR (95%CI) in the recessive genetic model.

b the value of OR (95%CI) in the additive genetic model. Pperm denoted empirical significance values on the basis of 10,000 permutations in the recessive and additive genetic models, respectively. PFDR-BH denoted the P-value after performing multiple testing corrections with FDR-BH method.