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Table 4 Multiple-SNP variants for TLR2, TLR4 and TLR9 polymorphisms and the occurrence of congenital HCMV infection

From: TLR2 2258 G>A single nucleotide polymorphism and the risk of congenital infection with human cytomegalovirus

TLR gene’s polymorphisms

Multiple-SNPa variant

Prevalence rates of multiple-SNP variants

ORb (95% CIc)

P-valued

Infected cases

Uninfected controls

TLR2 2258 G>A – TLR4 896 C>T

GA

0.850

0.874

1.00

 

GG

0.025

0.109

0.39 (0.06–2.59)

0.330

AA

0.125

0.016

8.81 (0.93–83.12)

0.063

TLR2 2258 G>A – TLR4 1196 C>T

GC

0.875

0.859

1.00

 

AC

0.125

0.016

8.03 (0.85–75.63)

0.075

TLR2 2258 G>A – TLR9 2848 G>A

GA

0.400

0.576

1.00

 

GG

0.475

0.408

1.62 (0.58–4.53)

0.360

AA

0.125

0.016

11.58 (1.19–112.59)

0.040

  1. P ≤ 0.050 is considered as significant
  2. a SNPs single nucleotide polymorphisms
  3. b OR odds ratio
  4. c 95% CI confidence interval
  5. dlogistic regression model