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. 2016 Nov 4;7(49):80935–80942. doi: 10.18632/oncotarget.13111

Table 2. The comparison of the genotypes and alleles of eight study polymorphisms between HCC patients and controls.

Polymorphisms Class WW WM MM *P M P
rs199514452 AA AT TT T
c.31T > A Patients 170 78 9 0.847 18.66% 0.837
Controls 175 82 7 18.18%
rs201540428 TT TA AA A
c.34A > T Patients 163 84 10 0.754 20.23% 0.447
Controls 159 93 12 22.16%
rs201614260 CC CG GG G
c.84G > C Patients 218 39 0 0.043 7.59% 0.039
Controls 240 24 0 4.55%
rs17879702 CC CT TT T
c.133C > T Patients 201 52 4 0.021 11.67% 0.007
Controls 230 32 2 6.82%
rs17880292 GG GA AA A
c.256G > A Patients 215 42 0 0.177 8.17% 0.673
Controls 221 39 4 8.90%
rs17879599 GG GC CC C
c.299G > C Patients 129 113 15 < 0.001 27.82% < 0.001
Controls 177 76 11 18.56%
rs17424145 TT TC CC C
c.341T > C Patients 227 30 0 0.311 5.84% 0.277
Controls 241 23 0 4.36%
rs35445101 AA AG GG G
c.790T > C Patients 213 43 1 0.247 8.75% 0.193
Controls 210 49 5 11.17%

Abbreviations: WW, homozygous wild genotype; WM, heterozygous genotype; MM, homozygous mutant genotype; M, mutant allele. P was calculated by the *Fisher's exact test for genotype comparisons and by the χ2-test for allele comparisons between patients and controls.