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. 2021 Apr 20;21:129. doi: 10.1186/s12890-021-01498-3

Table 5.

The relationship of FGFR2 and MGAT5 SNPs with COPD risk stratified by BMI

Gene SNP Model Genotype BMI ≤ 24
Frequency in case Frequency in control OR (95% CI) p
FGFR2 rs2420915 Allele G 0.586 0.627 1.00
A 0.414 0.373 1.19 (0.80–1.76) 0.392
Codominant GG 0.320 0.373 1.00
AA 0.148 0.120 1.58 (0.64–3.92) 0.324
AG 0.532 0.507 1.19 (0.65–2.17) 0.574
Dominant GG 0.320 0.373 1.00
AA + AG 0.680 0.627 1.26 (0.71–2.24) 0.429
Recessive AG + GG 0.852 0.880 1.00
AA 0.148 0.120 1.43 (0.62–3.31) 0.406
Additive 1.24 (0.81–1.88) 0.318
FGFR2 rs1907240 Allele A 0.574 0.597 1.00
G 0.426 0.403 1.10 (0.75–1.62) 0.632
Codominant AA 0.348 0.328 1.00
GG 0.200 0.135 1.43 (0.60–3.41) 0.419
GA 0.452 0.537 0.79 (0.43–1.46) 0.452
Dominant AA 0.348 0.328 1.00
GG + GA 0.652 0.672 0.92 (0.51–1.64) 0.771
Recessive GA + AA 0.800 0.865 1.00
GG 0.200 0.135 1.64 (0.75–3.60) 0.215
Additive 1.10 (0.75–1.63) 0.626
FGFR2 rs2257129 Allele C 0.586 0.597 1.00
T 0.414 0.403 1.05 (0.71–1.54) 0.824
Codominant CC 0.341 0.328 1.00
TT 0.169 0.135 1.23 (0.51–2.97) 0.641
TC 0.490 0.537 0.86 (0.47–1.59) 0.641
Dominant CC 0.341 0.328 1.00
TT + TC 0.659 0.672 0.94 (0.52–1.68) 0.827
Recessive TC + CC 0.831 0.865 1.00
TT 0.169 0.135 1.35 (0.61–2.99) 0.466
Additive 1.05 (0.70–1.57) 0.811
MGAT5 rs6430491 Allele G 0.639 0.604 1.00
A 0.361 0.396 0.86 (0.58–1.27) 0.456
Codominant GG 0.386 0.403 1.00
AA 0.108 0.194 0.48 (0.21–1.08) 0.075
AG 0.506 0.403 1.19 (0.65–2.20) 0.572
Dominant GG 0.386 0.403 1.00
AA + AG 0.614 0.597 0.96 (0.54–1.69) 0.888
Recessive AG + GG 0.892 0.806 1.00
AA 0.108 0.194 0.43 (0.20–0.920 0.029
Additive 0.78 (0.51–1.18) 0.231
MGAT5 rs2593704 Allele C 0.791 0.657 1.00
G 0.209 0.343 0.51 (0.33–0.77) 0.001
Codominant CC 0.633 0.433 1.00
GG 0.052 0.119 0.31 (0.12–0.83) 0.020
GC 0.315 0.448 0.52 (0.29–0.94) 0.031
Dominant CC 0.633 0.433 1.00
GG + GC 0.367 0.567 0.48 (0.27–0.83) 0.009
Recessive GC + CC 0.948 0.881 1.00
GG 0.052 0.119 0.41 (0.16–1.05) 0.064
Additive 0.54 (0.36–0.83) 0.005

SNP single nucleotide polymorphism, OR odds ratio, 95% CI 95% confidence interval

p values were calculated by logistic regression analysis with adjustment for age and gender

Bold values indicate statistical significance (p < 0.05)