Barely Significant
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De novo variants in exomes of congenital heart disease patients identify risk genes and pathways.

Genome Med · 2020 · PMC6961332 · PMID 31941532

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highly significantno p-value reported
Enrichment in cardiovascular disease categories To investigate the causal relatedness between the identified genes and biological functions/diseases, we analyzed the IPA-predicted top enriched diseases/functions categories (FDR < 0.05) and observed cardiovascular disease as a highly significant disease category in CHD cases (FDR = 5.36 × 10 −13 ) (Additional file 3 : Table S8).

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