Barely Significant
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Mutations in the Filaggrin are Predisposing Factor in Korean Children With Atopic Dermatitis.

Allergy Asthma Immunol Res · 2013 · PMC3695235 · PMID 23814674

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highly significantno p-value reported
8 reported that the R501X and 2282del4 nonsense mutations were associated with a highly significant dominant risk of AD in many European populations.

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