Table A3. .
Denmark |
Iowa |
Combined |
|||||||||||||
Gene/SNP and Phenotype |
RR1 | RR2 | LRT with 2 df (P) |
R_A | Additive Model LRT with 1 df (P) |
RR1 | RR2 | LRT with 2 df (P) |
R_A | Additive Model LRT with 1 df (P) |
RR1 | RR2 | LRT with 2 df (P) |
R_A | Additive Model LRT with 1 df (P) |
CYP1B1_snp1: | |||||||||||||||
Alla | 1.2 | 1.2 | .53 | 1.1 | .45 | .7 | .8 | .03 | 1.0 | .71 | 1.0 | 1.0 | .54 | 1.0 | .71 |
CL/P | 1.2 | 1.2 | .60 | 1.1 | .42 | .6 | .7 | .05 | .8 | .22 | .9 | 1.0 | .72 | 1.0 | 1.00 |
CPO | 1.0 | .9 | .93 | .9 | .70 | 1.3 | 2.5 | .04 | 1.7 | .02 | 1.1 | 1.4 | .37 | 1.2 | .23 |
CYP1A1: | |||||||||||||||
Alla | .6 | .8 | .03 | .7 | .01 | .7 | 1.1 | .20 | .8 | .17 | .7 | 1.0 | .006 | .7 | .007 |
No anomaliesb | .7 | 1.0 | .11 | .7 | .068 | .6 | .8 | .09 | .7 | .05 | .7 | .9 | .01 | .7 | .008 |
CYP1A2: | |||||||||||||||
CPO | 2.1 | .8 | .005 | 1.5 | .05 | 1.4 | 1.2 | .58 | 1.3 | .41 | 1.7 | 1.3 | .01 | 1.4 | .03 |
GSTA4_snp2: | |||||||||||||||
No anomaliesb | .7 | .8 | .007 | .7 | .01 | 1.0 | 1.4 | .61 | 1.1 | .61 | .8 | 1.0 | .04 | .9 | .11 |
CLO | .6 | 1.7 | .005 | .9 | .40 | .6 | .5 | .12 | .6 | .06 | .6 | 1.2 | .001 | .8 | .07 |
GSTM1_snp1: | |||||||||||||||
CPO | 1.3 | 3.5 | .02 | 1.7 | .01 | 1.1 | 1.1 | .98 | 1.1 | .82 | THRRc | ||||
GSTP1_snp3: | |||||||||||||||
Alla | 1.1 | 1.0 | .47 | 1.0 | .86 | 1.2 | .6 | .01 | .9 | .19 | THRRc | ||||
CL/P | 1.1 | 1.1 | .60 | 1.0 | .70 | 1.1 | .5 | .01 | .8 | .16 | THRRc | ||||
NAT2_snp2: | |||||||||||||||
Alla | .8 | .6 | .04 | .8 | .01 | .8 | .6 | .12 | .8 | .04 | .8 | .6 | .006 | .8 | .001 |
No anomaliesb | .8 | .6 | .07 | .8 | .02 | .8 | .6 | .20 | .8 | .07 | .8 | .6 | .01 | .8 | .003 |
CL/P | .8 | .4 | .01 | .7 | .01 | .9 | .6 | .43 | .8 | .24 | .8 | .5 | .007 | .7 | .002 |
Control | .7 | .8 | .01 | .8 | .02 | 1.0 | .8 | .67 | .9 | .43 | .8 | .8 | .03 | .8 | .02 |
Note.— RR1 is the genetic RR when the child carries one copy of the variant allele; RR2 is that when the child carries two copies of the variant alleles; R_A is the RR when the child carries one copy of the variant allele, assumed to be a log additive model, a model in which the RR of carrying two copies of the variant alleles is the square of that of carrying one copy.
Includes data from all subjects with nonsyndromic OC.
Includes data from subjects without other minor anomalies.
For test of heterogeneity in RR (THRR), P<.05.