TCF7L1 Genetic Variants Are Associated with the Susceptibility to Cervical Cancer in a Chinese Population
Table 4
Association analysis between TCF7L1 SNPs and cervical cancer risk.
SNP ID
Model
Genotype
Case
Control
Without adjusted
With adjusted
OR (95% CI)
a
OR (95% CI)
b
rs11904127
Allele
G
644
564
1
A
368
408
0.79 (0.66-0.95)
0.010
Codominant
GG
209
157
1
1
GA
226
250
0.68 (0.52-0.89)
0.006
0.68 (0.52-0.89)
0.006
AA
71
79
0.68 (0.46-0.99)
0.044
0.67 (0.46-0.99)
0.043
Dominant
GG
209
157
1
1
AG-AA
297
329
0.68 (0.52-0.88)
0.003
0.68 (0.52-0.88)
0.003
Recessive
GG-AG
435
407
1
1
AA
71
79
0.84 (0.59-1.19)
0.329
0.84 (0.59-1.19)
0.323
Log-additive
—
—
—
0.79 (0.66-0.95)
0.010
0.79 (0.66-0.94)
0.010
rs2366264
Allele
G
716
677
1
T
298
309
0.91 (0.75-1.10)
0.343
Codominant
GG
249
233
1
1
GT
218
211
0.97 (0.75-1.25)
0.799
0.97 (0.74-1.25)
0.797
TT
40
49
0.76 (0.49-1.20)
0.245
0.76 (0.48-1.20)
0.244
Dominant
GG
249
233
1
1
TG-TT
258
260
0.93 (0.72-1.19)
0.558
0.93 (0.72-1.19)
0.556
Recessive
GG-TG
467
444
1
1
TT
40
49
0.78 (0.50-1.20)
0.256
0.78 (0.50-1.20)
0.256
Log-additive
—
—
—
0.91 (0.75-1.10)
0.340
0.91 (0.75-1.10)
0.338
rs11689667
Allele
T
719
674
1
C
293
312
0.88 (0.73-1.07)
0.191
Codominant
TT
253
230
1
1
TC
213
214
0.90 (0.70-1.17)
0.452
0.90 (0.70-1.17)
0.447
CC
40
49
0.74 (0.47-1.17)
0.198
0.74 (0.47-1.17)
0.198
Dominant
TT
253
230
1
1
TC-CC
253
263
0.87 (0.68-1.12)
0.290
0.87 (0.68-1.12)
0.287
Recessive
TT-TC
466
444
1
1
CC
40
49
0.78 (0.50-1.21)
0.260
0.78 (0.50-1.21)
0.261
Log-additive
—
—
—
0.88 (0.73-1.07)
0.188
0.88 (0.72-1.07)
0.187
rs62162674
Allele
G
711
654
1
C
301
336
0.82 (0.68-0.99)
0.044
Codominant
GG
245
210
1
1
GC
221
234
0.81 (0.62-1.05)
0.112
0.81 (0.62-1.05)
0.107
CC
40
51
0.67 (0.43-1.06)
0.086
0.67 (0.43-1.06)
0.085
Dominant
GG
245
210
1
1
CG-CC
261
285
0.79 (0.61-1.01)
0.057
0.78 (0.61-1.01)
0.054
Recessive
GG-CG
466
444
1
1
CC
40
51
0.75 (0.48-1.15)
0.188
0.75 (0.48-1.15)
0.189
Log-additive
—
—
—
0.82 (0.67-0.99)
0.039
0.81 (0.67-0.99)
0.038
CI: confidence interval; OR: odds ratio; SNP: single nucleotide polymorphism. a values were calculated by logistic regression analysis without adjustment. b values were calculated by logistic regression analysis with adjustment for age. indicates statistical significance.