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. 2014 Oct 1;18(10):703–710. doi: 10.1089/gtmb.2014.0028

Table 3.

Genotype Frequencies of ERCC2 Gene Polymorphisms in Controls and Cases and Their Associations with Breast Cancer

SNPs Genotype Case n (%) Control n (%) OR (95% CI)a p-Value pc
rs3916840 CC 91 (90.1) 90 (89.1) Reference    
  CT 10 (9.9) 11 (10.9) 0.889 (0.364–2.222) 0.818 NS
  TT 0 0      
  C 192 (95.1) 191 (94.6) Reference    
  T 10 (4.9) 11 (5.4) 0.904 (0.375–2.179) 0.823 NS
rs1799793 GG 84 (83.2) 89 (88.1) Reference    
  GA 17 (16.8) 12 (11.9) 1.501 (0.667–3.330) 0.316 NS
  AA 0 0      
  G 185 (91.6) 190 (94.1) Reference    
  A 17 (8.4) 12 (5.9) 1.455 (0.676–3.130) 0.335 NS
rs238416 GG 52 (51.5) 25 (24.7) Reference    
  GA 37 (36.6) 62 (61.4) 0.287 (0.153–0.537) <0.001 <0.01
  AA 12 (11.9) 14 (13.9) 0.412 (0.166–1.020) 0.052 NS
  G 141 (69.8) 112 (55.4) Reference    
  A 61 (30.2) 90 (44.6) 0.538 (0.358–0.810) 0.003 0.027
  Dominantb     0.310 (0.171–0.563) <0.001 <0.01
  Recessivec     0.838 (0.367–1.913) 0.674 NS
a

ORs were adjusted for age of onset.

b

The dominant model: comparing the combination of heterozygotes and minor allele homozygotes with the major allele homozygotes.

c

The recessive model: comparing minor allele homozygotes with the combination of heterozygotes and major allele homozygotes.

CI, confidence interval; ERCC2, excision repair cross-complementing group 2; NS, not significant; OR, odds ratio; pc, corrected p-value (after Bonferroni multiple adjustment).