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Table 4 Association between SNPs and SVD using the additive, genotype, dominant, and the recessive models

From: Association study of polymorphisms in the ABO gene with ischemic stroke in the Chinese population

SNP Model Allele or geno case control Unadjusted OR (95 % CI) Unadjusted
p-value
Adjusted
OR (95 % CI)
Adjusted p-value
rs579459 Additive C/T 166/734 334/1576 1.07 (0.87-1.31) 0.54 1.08 (0.85-1.39) 0.53
  Dominant CC + CT/TT 152/298 300/655 1.11 (0.88-1.41) 0.38 1.10 (0.83-1.47) 0.51
  Recessive CC/CT + TT 14/436 34/921 0.87 (0.46-1.64) 0.67 1.09 (0.51-2.32) 0.83
rs651007 Additive T/C 156/718 337/1575 1.02 (0.82-1.25) 0.89 1.03 (0.80-1.33) 0.80
  Dominant TT + CT/CC 144/293 304/652 1.05 (0.83-1.34) 0.67 1.04 (0.78-1.39) 0.81
  Recessive TT/CT + CC 12/425 33/923 0.79 (0.40-1.54) 0.49 1.05 (0.47-2.32) 0.91
rs529565 Additive C/T 305/569 709/1201 0.91 (0.77-1.07) 0.26 0.94 (0.77-1.14) 0.51
  Dominant CC + CT/TT 245/192 565/390 0.88 (0.70-1.11) 0.28 0.87 (0.66-1.15) 0.33
  Recessive CC/CT + TT 60/377 144/811 0.90 (0.65-1.24) 0.51 1.01 (0.69-1.50) 0.95
  1. All SNPs were analyzed under additive, genotype, dominant (Dom) and recessive (Rec) models; OR: odds ratio; CI: confidence interval; unadjusted P-value from t-test; adjusted P-value using logistic regression analysis with age, gender, hypertension, diabetes, and dyslipidemia as covariates. Significant P values (p < 0.05) are in bold and p* < 0.017 (Bonferroni multiple correction threshold)