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. 2019 Jan 7;19:24. doi: 10.1186/s12885-018-5149-0

Table 1.

The genotype distribution and H-W of XRCC1 (rs25487), TP53 (rs1042522) and FGFR3 (rs121913483)

Variable Alleles Phenotype N HWE MAF M/M (%) M/m (%) m/m (%) M/M +M/m M/m +m/m Allele M Allele m
rs25487 G > A Cases 121 0.18 0.40 47(38.9) 51(42.1) 23(19) 98 74 145(59.9) 97(40.1)
NC 118 0.15 0.25 70(59.3) 38(32.2) 10(8.5) 108 48 178(75.4) 58(24.6)
OC 101 0.45 0.27 55(54.4) 37(36.6) 9(9) 92 46 147(72.8) 55(27.2)
rs1042522 G > C Cases 121 0.18 0.38 50(41.3) 50(41.3) 21(17.4) 100 71 150(62) 92(38)
NC 108 0.74 0.42 37(34.3) 51(47.2) 20(18.5) 88 71 125(57.9) 91(42.1)
OC 99a 0.07 0.44 35(35.4) 40(40.4) 24(24.2) 75 64 110(55.6) 88(44.4)
rs121913483 G > C Cases 117 117 0 0
NC 113 113 0 0
OC 89 89 0 0

N Number, HWE Hardy-Weinberg equilibrium, MAF Minor allele frequency, NC Negative controls, OC Old controls

aThe number of subjects in each group at different sites may be different due to insufficient DNA