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. 2020 Mar 16;13:73–86. doi: 10.2147/CEG.S232961

Table 7.

Haplotype Frequencies of XRCC1 Gene Polymorphisms and Their Association with the Risk of Esophageal Cancer

Haplotype XRCC1 p.Arg399Gln-p.Arg280His-p.Arg194Trp Studied Population % (n)(497) Cases N Controls χ2 (p value)* Odds Ratio (OR)(95% CI) p value**
G-G-C 0.501(249) 0.508(108) 0.496(141) 0.1 (p=0.7) Reference
A-G-C 0.347(174) 0.314(67) 0.372(107) 3.6 (p=0.05) 0.82(0.6–1.2) p=0.3
G-G-T 0.075(37) 0.096(20) 0.058(17) 5.0(p=0.02) 1.5(0.7–3.1) p= 0.1
G-A-C 0.055(27) 0.060(13) 0.052(14) 0.3(p=0.5) 1.2(0.5–2.7) p= 0.6
A-A-C 0.014(7) 0.015(3) 0.014(4) 0.02(p=0.8) 0.9(0.2–4.4) p=0.9
A-G-T 0.008(4) 0.007(2) 0.008(2) 0.07(p=0.7) 1.3(0.2–9.4) p=0.8
LD Measures Esophageal Cancer Patients
D̍̀ r2
p.Arg399Gln-p.Arg194Trp 0.845 0.042 0.596
p.Arg280His-p.Arg194Trp 1.0 0.009 0.969
p.Arg399Gln-p.Arg280His 0.188 0.001 0.633

Notes: P* Comparison for esophageal cancer patients and controls for each haplotype. P** Comparison for esophageal cancer patients and controls in comparison to the wild type genotype taken as reference, P<0.05 taken as statistically significant (bold values).