Barely Significant
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Prenatal diagnosis of recurrent hypoplastic left heart syndrome associated with MYH6 variants: a case report.

BMC Cardiovasc Disord · 2023 · PMC9993643 · PMID 36890431

Europe PMCDOI
1
hedged sentence
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

The sentences

highly significantp = 0.000068actually significant
More recently, whole-genome sequencing revealed a highly significant ( p = 0.000068), abnormally high proportion of pathogenic MYH6 variants observed in 197 patients with HLHS (vs. 813 controls) [ 13 ].

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