Association of TLR3 L412F Polymorphism with Cytomegalovirus Infection in Children.

PLoS One · 2017 · PMC5207783 · PMID 28046022

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highly significantno p-value reported

In individuals with a mutation present in at least one allele of the L412F SNP, an increased risk of HCMV disease was found, and this result remained highly significant after Bonferroni’s correction for multiple testing ( P c < 0.001).

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did not reach statistical significanceno p-value reported

Moreover, those with a heterozygous genotype of rs3775296 showed an increased relative risk of HCMV infection ( P = 0.042), but this association did not reach statistical significance after correction for multiple testing.

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