Barely Significant
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Sex-aware genome-wide assessment of de novo variants in autism across coding and noncoding regions.

Hum Genomics · 2026 · PMC13248286 · PMID 42032772

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hedged sentence
closest p
boldest claim

The sentences

close to significanceno p-value reported
While not exome-wide significant, this is a gene that may be of interest in future studies as it is the only one that was not an X chromosome gene that was close to significance.

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