Barely Significant
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Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa.

Mol Psychiatry · 2018 · PMC5828108 · PMID 29155802

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The sentences

nominally significantP <0.05actually significant
Twelve signals passed QC and were polymorphic in the de novo genotyping cohort, of which four were nominally significant ( Supplementary Table 6 ; P <0.05, minimum P =0.001).

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