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. 2014 Jan 16;5(1):e46. doi: 10.1038/ctg.2013.17

Table 1. Discovery cohort association analyses of 17 NOS2 SNPs with VEO-IBD.

            Recessive association
Chr. SNP Position MAF FU FA P-value OR L95 U95
17 rs2297518 23120724 0.18 0.23 0.17 6.2 × 10−6 4.43 2.32 8.46
17 rs1137933 23130059 0.21 0.27 0.21 7.4 × 10−4 2.64 1.50 4.65
17 rs9906835 23113501 0.42 0.38 0.43 0.39 0.81 0.51 1.29
17 rs944725 23133698 0.41 0.50 0.40 0.03 1.56 1.03 2.34
17 rs3730013 23150045 0.34 0.29 0.34 0.19 0.67 0.36 1.22
17 rs4795067 23130802 0.33 0.35 0.33 0.08 1.48 0.94 2.33
17 rs2297516 23119857 0.42 0.38 0.42 0.91 1.02 0.66 1.58
17 rs3794764 23135555 0.23 0.21 0.23 0.71 0.86 0.40 1.86
17 rs8072199 23140975 0.44 0.51 0.44 0.482 1.16 0.76 1.75
17 rs10459953 23151645 0.35 0.33 0.35 0.93 1.02 0.61 1.65
17 rs2314809 23119505 0.40 0.36 0.40 0.92 0.97 0.62 1.53
17 rs11080344 23128638 0.46 0.44 0.46 0.09 1.39 0.94 2.05
17 rs3794756 23110756 0.01 0.02 0.01 NA NA NA NA
17 rs3729508 23133157 0.40 0.38 0.40 0.96 1.01 0.64 1.58
17 rs11653716 23108659 0.032 0.05 0.03 NA NA NA NA
17 rs2314810 23128237 0.04 0.04 0.04 0.56 1.93 0.19 18.71
17 rs3730017 23133229 0.020 0.02 0.02 NA NA NA NA

FA, frequency affected; FU, frequency unaffected; L95 and U95, lower and upper 95th confidence interval; MAF, minor allelic frequency.

P values are presented as uncorrected and recessive modeling.