Barely Significant
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Meta-analysis of whole-exome sequencing data from two independent cohorts finds no evidence for rare variant enrichment in Parkinson disease associated loci.

PLoS One · 2020 · PMC7529297 · PMID 33002040

Europe PMCDOI
1
hedged sentence
0.0500
closest p · 1.0× alpha
0.0500
boldest claim

The sentences

nominally significantp < 0.05actually significant
Gene-based analyses indicated three genes with nominally significant p-values (uncorrected p < 0.05) across multiple cohorts: GALC , SEC23IP and PARP9 .

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