Barely Significant
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Patterns and functional implications of rare germline variants across 12 cancer types.

Nat Commun · 2015 · PMC4703835 · PMID 26689913

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nearly significantno p-value reported
With respect to genes, we first tested the expanded list of 34 significant or nearly significant genes (known and likely oncogenes excluded) in burden analysis (see Methods) for evidence of somatic loss of the WT allele.

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