Barely Significant
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De Novo Variants Predominate in Autism Spectrum Disorder.

Genes (Basel) · 2025 · PMC12470000 · PMID 41010044

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highly significantno p-value reported
The three comparisons in the Abstract section regarding silent variants are all post-analysis; thus, these should be considered to be putative despite remaining highly significant following Bonferroni corrections.

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