Barely Significant
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Widespread genomic influences on phenotype in Dravet syndrome, a 'monogenic' condition.

Brain · 2023 · PMC10473570 · PMID 37006128

1
hedged sentence
0.8900
closest p · 17.8× alpha
0.8900
boldest claim

The sentences

did not reach statistical significanceP = 0.89not close (p > 0.1)
The epilepsy PRS was higher in the Dravet syndrome cohort compared with the GEL epilepsy and GEL controls, although this did not reach statistical significance (adjusted P = 0.89, at PT = 10 −2 , and adjusted P = 0.11, at PT = 10 −2 , Tukey’s test, respectively).

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