Table 2—

Genotyping and association results of chronic obstructive pulmonary disease under a codominant model

GeneCommon nameControlsCasesORAdjusted OR
nMAFGenotypes %p-value#nMAFGenotypes %Het ORHom ORp-valueHet ORHom ORp-value+
1–11–22–21–11–22–2
EPHX1Tyr113His2410.315039110.292390.30464951.340.500.021.260.510.06
His139Arg2460.22613550.852380.22613541.010.941.001.010.890.97
TNF−308 G>A2440.20653050.422400.20643151.040.940.990.931.090.91
−376 G>A2450.0198201.002420.0198200.81NA0.871.21NA0.78
−238 G>A2440.0492801.002420.05901001.25NA0.471.57NA0.19
ADRB2Gln27Glu2450.472753200.442440.452954180.960.810.731.060.860.71
Gly16Arg2390.403846170.502380.413351161.261.080.501.320.990.34
  • OR: odds ratio; MAF: minor allele fraction; Het OR: heterozygote OR; Hom OR: OR homozygote for minor allele; EPHX1: microsomal epoxide hydroxylase; TNF: tumour necrosis factor; ADRB2: β2-adrenoreceptor; NA: not applicable or computable, due to a sparse 2×2 table. #: p-value from test for Hardy–Weinberg equilibrium in controls; : p-values from Fisher's exact test; +: p-values from logistic regression, adjusted for age, pack-yrs and sex.