Barely Significant
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Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.

Nat Commun · 2023 · PMC10359300 · PMID 37474567

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nominally significantno p-value reported
Across the 32 detected credible intervals and 1667 annotated HPO concepts, we identified 622 nominally significant associations (two-sided Fisher’s exact test, Supplementary Data 3 ).

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