Whole Exome Sequencing in Healthy Individuals of Extreme Constitution Types Reveals Differential Disease Risk: A Novel Approach towards Predictive Medicine.

J Pers Med · 2022 · PMC8952204 · PMID 35330488

Europe PMC DOI

hedged sentence

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closest p · 0.0× alpha

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boldest claim

The sentences

highly significantp -value < 2.537 × 10 −15actually significant

Interestingly, these SNP numbers are highly significant when compared to any random SNP set intersection with the GWAS catalog ( p -value < 2.537 × 10 −15 ).

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