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. 2020 Mar 24;34(8):e23311. doi: 10.1002/jcla.23311

TABLE 2.

Association between H19 gene rs2839698 polymorphism and colorectal cancer risk determined by logistic regression analyses

Models Genotype Case (n, %) Control (n, %) OR (95% CI) P‐value OR (95% CI)* P‐value*
Co‐dominant GG 134 (42.7%) 154 (35.1%) 1.00 1.00
Heterozygote GA 140 (44.6%) 211 (48.1%) 0.77 (0.56‐1.05) .098 0.72 (0.50‐1.02) .062
Homozygote AA 40 (12.7%) 74 (16.9%) 0.62 (0.40‐0.97) .038 0.63 (0.38‐1.02) .062
Dominant GG 134 (42.7%) 154 (35.1%) 1.00 1.00
AA + GA 180 (57.3%) 285 (64.9%) 0.73 (0.54‐0.98) .037 0.69 (0.50‐0.96) .030
Recessive GA + GG 274 (87.3%) 365 (83.1%) 1.00 1.00
AA 40 (12.7%) 74 (16.9%) 0.72 (0.47‐1.09) .118 0.75 (0.48‐1.18) .214
Allele G 408 (65.0%) 519 (59.1%) 1.00
A 220 (35.0%) 359 (40.9%) 0.78 (0.63‐0.96) .021

The genotyping was successful in 314 cases and 439 controls for rs2839698 polymorphism; Bold values are statistically significant (P < .05).

*

Adjustment for age, sex, BMI, alcohol, and smoking.