Barely Significant
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Large-Scale Whole Genome Sequence Analysis of >22,000 Subjects Provides no Evidence of <i>FMR1</i> Premutation Allele Involvement in Autism Spectrum Disorder.

Genes (Basel) · 2023 · PMC10454383 · PMID 37628570

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hedged sentence
0.0100
closest p · 0.2× alpha
0.0100
boldest claim

The sentences

nominally significantp -value = 0.010actually significant
The prevalence of FMR1 premutation carriers in the parents of the SSC cohort compared to the prevalence observed in samples from the MRGB ( Figure 3 C) were significantly higher for mothers ( p -value = 4.057 × 10 −5 ) and nominally significant for fathers ( p -value = 0.010).

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