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. 2012 Sep 18;23(2):242–253. doi: 10.1038/cr.2012.135

Table 2. Stratification analysis of CBS −4673C>G genotypes according to CHD classification and phenotype. The used controls were the total 2 270 combined controls.

Variable Case number P value Association [OR (95% CI)]1
CG vs CC GG vs CC
CHD Classification I 2
Conotruncal defects 386 0.002 0.69 (0.55-0.88) 0.63 (0.44-0.91)
Septation defects 1 652 1.29 × 10−6 0.92 (0.81-1.05) 0.57 (0.46-0.71)
LVOTO 47 0.51 0.69 (0.36-1.30) 0.85 (0.36-2.01)
RVOTO 75 0.98 0.97 (0.59-1.59) 0.92 (0.45-1.91)
APVR 14 0.006 0.08 (0.01-0.66) 0.54 (0.12-2.47)
Complex CHDs 34 0.01 0.30 (0.13-0.71) 0.69 (0.26-1.85)
Other CHDs 132 0.62 0.93 (0.64-1.35) 0.75 (0.42-1.35)
CHD Classification II
Isolated nonsyndromic CHD 2 025 3.2 × 10−7 0.86 (0.75-0.97) 0.58 (0.47-0.70)
Syndromic CHD 315 0.25 0.84 (0.64-1.08) 0.77 (0.53-1.14)
Isolated phenotype
ASD (atrial septal defect) 235 0.0006 0.89 (0.67-1.19) 0.37 (0.22-0.65)
VSD (ventricular septal defect) 1 220 3.18 × 10−5 0.93 (0.80-1.08) 0.58 (0.45-0.74)
TOF (tetralogy of Fallot) 291 0.0016 0.66 (0.50-0.85) 0.59 (0.39-0.89)

1Adjusted for age, sex;

2Classification described in16.