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Table 2 Distribution of genotypes and allelic frequencies of the NME1 rs34214448 and rs2302254 and DCC rs2229080 and rs714 variants in CRC and control group

From: NME1 and DCC variants are associated with susceptibility and tumor characteristics in Mexican patients with colorectal cancer

Genotype

CRC group

n = 232 (%)

Control group

n = 232 (%)

OR (95% CI)

P value

NME1 (rs34214448) G > T

G/G

51 (21.98)

99 (42.67)

1.00 (Reference)

 

G/T

144 (62.07)

104 (44.83)

2.68 (1.76- 4.09)

0.001

T/T

37 (15.95)

29 (12.50)

2.47 (1.37- 4.47)

0.001

G/T + T/T vs. G/G

181 (78.02)

170 (57.33)

2.06 (1.38 – 3.07)

0.001

Allele

G

246 (53.02)

302(65.09)

1.00 (Reference)

 

T

218 (46.98)

162(34.91)

1.65 (1.26 – 2.151)

0.001

NME1 (rs2302254) C > T

C/C

54 (23.28)

65 (28.02)

1.00 (Reference)

 

C/T

124 (53.45)

125 (53.88)

1.19 (0.77 – 1.85)

0.495

T/T

54 (23.28)

42 (18.10)

1.54 (0.90 – 2.65)

0.147

C/T + T/T vs. C/C

178 (76.72)

167 (71.98)

1.28 (0.82 – 1.99)

0.287

Allele

C

232 (50.0)

255 (54.96)

1.00 (Reference)

 

T

232 (50.0)

209 (45.04)

1.22 (0.94 – 1.57)

0.148

DCC (rs2229080) G < C

G/G

48 (20.69)

78 (33.62)

1.00 (Reference)

 

G/C

128 (55.17)

104 (44.83)

2.00 (1.28 – 3.11)

0.002

C/C

56 (24.14)

50 (21.55)

1.82 (1.07 – 3.07)

0.034

G/C + C/C vs. G/G

184 (79.31)

154 (66.38)

1.94 (1.27 – 3.02)

0.002

Allele

G

224 (48.28)

260 (56.03)

1.00 (Reference)

 

C

240 (51.72)

204 (43.97)

1.36 (1.05 – 1.76)

0.021

DCC (rs714) A > G

A/A

45 (19.40)

57 (24.57)

1.00 (Reference)

 

A/G

130 (56.03)

108 (46.55)

1.52 (0.95—2.43)

0.097

G/G

57 (24.57)

67 (28.88)

1.07 (0.63—1.82)

0.885

A/G + G/G vs. A/A

187 (80.60)

175 (75.43)

1.35 (0.87 – 2.10)

0.217

Allele

A

220 (47.41)

222 (47.41)

1.00 (Reference)

 

G

244 (52.59)

242 (52.59)

1.01 (0.78—1.31)

0.947

  1. P-value were adjusted by the Bonferroni test (0.0125); Bold text highlights statistically significant findings