Prioritization and functional assessment of noncoding variants associated with complex diseases.

Genome Med · 2018 · PMC6042373 · PMID 29996888

Europe PMC DOI

hedged sentence

0.0000

closest p · 0.0× alpha

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boldest claim

The sentences

extremely significantp ≤ 10E−8actually significant

Twenty four thousand nine hundred ninety-three cSNPs from GWASdb were selected as extremely significant variants using a threshold of p ≤ 10E−8.

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