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Table 2 Association between SNPs and ischemic stroke 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 363/1455 334/1576 1.18 (1.00-1.39) 0.05 1.18 (0.97-1.43) 0.10
  Dominant CC + CT/TT 326/583 300/655 1.22 (1.00-1.48) 0.04 1.20 (0.95-1.52) 0.12
  Recessive CC/CT + TT 37/872 34/921 1.15 (0.71-1.85) 0.57 1.31 (0.74-2.31) 0.36
rs651007 Additive T/C 349/1421 337/1575 1.15 (0.97-1.36) 0.10 1.15 (0.94-1.40) 0.17
  Dominant TT + CT/CC 314/571 304/652 1.18 (0.97-1.43) 0.09 1.16 (0.92-1.46) 0.22
  Recessive TT/CT + CC 35/850 33/923 1.15 (0.71-1.87) 0.57 1.35 (0.76-2.40) 0.31
rs529565 Additive C/T 679/1087 709/1201 1.06 (0.93-1.21) 0.41 1.06 (0.90-1.24) 0.48
  Dominant CC + CT/TT 540/343 565/390 1.09 (0.90-1.31) 0.38 1.08 (0.86-1.35) 0.52
  Recessive CC/CT + TT 139/744 144/811 1.05 (0.82-1.36) 0.69 1.08 (0.79-1.47) 0.62
  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)