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. 2016 Nov 26;66(3):309–318. doi: 10.1007/s00262-016-1936-0

Table 3.

Association of genotypes with the occurrence of precancerous lesions

SNP Model Genotype Patient (n, %) Control (n, %) OR (95% CI) P value
rs10815225 Codominant G/G 133 (85.8) 411 (82.2) 1 0.11
G/C 21 (13.6) 89 (17.8) 0.73 (0.44–1.22)
C/C 1 (0.6) 0 (0) NA (0.00-NA)
Dominant G/G 133 (85.8) 411 (82.2) 1 0.29
G/C–C/C 22 (14.2) 89 (17.8) 0.76 (0.46–1.27)
Recessive G/G–G/C 154 (99.3) 500 (100) 1 0.089
C/C 1 (0.6) 0 (0) NA (0.00-NA)
Overdominant G/G–C/C 134 (86.5) 411 (82.2) 1 0.21
G/C 21 (13.6) 89 (17.8) 0.72 (0.43–1.21)
rs4143815 Codominant C/C 30 (19.5) 160 (32) 1 0.0013
G/C 69 (44.8) 223 (44.6) 1.65 (1.032.65)
G/G 55 (35.7) 117 (23.4) 2.51 (1.514.15)
Dominant C/C 30 (19.5) 160 (32) 1 0.0021
G/C-G/G 124 (80.5) 340 (68) 1.95 (1.253.02)
Recessive C/C-G/C 99 (64.3) 383 (76.6) 1 0.003
G/G 55 (35.7) 117 (23.4) 1.82 (1.232.68)
Overdominant C/C-G/G 85 (55.2) 277 (55.4) 1 0.96
G/C 69 (44.8) 223 (44.6) 1.01 (0.70–1.45)

Significant results are shown in bold (P < 0.05)