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. 2018 May 26;24:3488–3495. doi: 10.12659/MSM.907524

Table 2.

Logistic regression analysis and genotype frequency of polymorphisms in IL-1α gene between HCC and control.

SNP locus HWE Genotype HCC Control Model OR (95% CI) P-value
n=178 n=397
rs3783550
Intron
0.51 C/C 67 (53.2%) 186 (50.1%) Codominant 0.81 (0.55–1.21) 0.31
A/C 51 (40.5%) 157 (42.3%) Dominant 0.86 (0.52–1.43) 0.56
A/A 8 (6.3%) 28 (7.5%) Recessive 0.51 (0.19–1.38) 0.18
rs17561
missense (Ser114Ala)
0.68 G/G 163 (92.6%) 350 (88.2%) Codominant 0.50 (0.24–1.06) 0.06
T/G 13 (7.4%) 45 (11.3%) Dominant 0.52 (0.24–1.14) 0.10
T/T 0 (0.0%) 2 (0.5%) Recessive 0.00 (0.00–NA) 0.11
rs1800587
5′-UTR
0.12 C/C 162 (91.5%) 349 (87.9%) Codominant 0.70 (0.35–1.39) 0.30
T/C 14 (7.9%) 45 (11.3%) Dominant 0.66 (0.31–1.39) 0.27
T/T 1 (0.6%) 3 (0.8%) Recessive 0.87 (0.06–12.77) 0.92
rs1800794
5′-nearGene
0.23 C/C 158 (91.9%) 350 (88.6%) Codominant 0.69 (0.34–1.39) 0.29
T/C 13 (7.6%) 43 (10.9%) Dominant 0.64 (0.30–1.39) 0.25
T/T 1 (0.6%) 2 (0.5%) Recessive 0.94 (0.06–14.63) 0.97

HWE is Hardy-Weinberg equilibrium. Genotype distributions are shown as number (%). Odds ratio (OR), 95% confidence interval (CI), and p-values were from logistic regression analysis with codominant, dominant, and recessive models controlling age and gender as covariates. SNP is single nucleotide polymorphism. Total number of each SNP is different, because genotypes of some SNPs are unreadable.