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. 2019 Aug 27;10(20):4860–4865. doi: 10.7150/jca.32675

Table 3.

Association of the 2 SNPs in MAGE-A11 gene and risk of RCC in totality and validation set.

Stages SNPs OR (95% CI)a Pb Bonferronic
Additive model Dominant model Recessive model Codominant model
het hom
Totality rs6641352 1.250 (1.069-1.461) 1.315 (1.089-1.588) 1.299 (0.855-1.975) 1.299 (1.066-1.583) 1.423 (0.931-2.174) 0.005 0.020
rs6540341 1.275 (1.102-1.476) 1.301 (1.081-1.564) 1.614 (1.123-2.320) 1.226 (1.009-1.491) 1.740 (1.202-2.519) 0.001 0.004
Validation rs6641352 1.309 (1.049-1.633) 1.456 (1.113-1.905) 1.112 (0.618-2.001) 1.489 (1.123-1.974) 1.269 (0.700-2.302) 0.017 0.068
rs6540341 1.298 (1.056-1.596) 1.317 (1.014-1.711) 1.717 (1.030-2.862) 1.228 (0.931-1.619) 1.852 (1.100-3.120) 0.013 0.052

Values in bold indicate are statistically different.

aLogistic regression model with adjustment for age, sex, BMI, smoking status, drinking status, hypertension, diabetes and family history of cancer in additive (rare homozygote versus heterozygote versus major homozygote) models, dominant (heterozygote/rare homozygote versus major homozygote), recessive (rare homozygote versus heterozygote/major homozygote) and codominant (het: heterozygote versus major homozygote; hom: rare homozygote versus major homozygote). BMI, body mass index; OR, odds ratio.

bAdjusted for age, sex, BMI, smoking status, drinking status, hypertension, diabetes and family history of cancer in additive model

cBonferroni correction for additive model.