Barely Significant
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Variant graph craft (VGC): a comprehensive tool for analyzing genetic variation and identifying disease-causing variants.

BMC Bioinformatics · 2024 · PMC11370019 · PMID 39227781

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nominally significantno p-value reported
For example, we demonstrate the visualization of variants in TTN, a gene with pathogenic, nominally significant variants identified in univariate analysis (Fig. 4 ).

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