Barely Significant
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Rare protein-coding variants implicate genes involved in risk of suicide death.

Am J Med Genet B Neuropsychiatr Genet · 2021 · PMC9292859 · PMID 34042246

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nominally significantno p-value reported
The average CADD PHRED score for the 2,528 nominally significant variants was 22.05 (6.25 SD ).

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