Barely Significant
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Thyroid peroxidase gene variants and susceptibility to congenital hypothyroidism and autoimmune thyroid disease among Egyptian pediatric cohort.

Clin Exp Pediatr · 2026 · PMC13244060 · PMID 41927052

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closest p · 0.0× alpha
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The sentences

highly significantP <0.001actually significant
This shift toward His-containing genotypes was highly significant ( P <0.001) and accompanied by markedly elevated odds ratios, indicating a strong risk effect of the His allele, particularly in homozygous form.

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