Barely Significant
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Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine.

Nat Commun · 2024 · PMC10847475 · PMID 38321032

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nominally significantp < 0.05actually significant
We then performed a pathway enrichment analysis on all 353 nominally significant ( p < 0.05) genes from the burden test (i.e., CVM-associated genes).

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