Barely Significant
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Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.

Ann Clin Transl Neurol · 2018 · PMC5899906 · PMID 29688227

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

The sentences

nominally significantP < 0.05actually significant
In addition, missense mutations in MYRF and ASRGL 1 under previously reported linkage peaks at 7q14.3 and 11q12.3 segregated completely in one family and in follow‐up genotyping both were nominally significant ( P < 0.05).

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