Barely Significant
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Polygenic risk scores and the need for pharmacotherapy in neonatal abstinence syndrome.

Pediatr Res · 2023 · PMC9931940 · PMID 35974158

1
hedged sentence
0.0420
closest p · 0.8× alpha
0.0420
boldest claim

The sentences

nominally significantp = 0.042actually significant
However, rs2614095 (intronic variant within PNOC ) was nominally significant in the present study (p = 0.042) and showed the same direction of affect across studies (minor allele A being protective).

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