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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)