Barely Significant
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Identification of candidate causal variants and target genes at 41 breast cancer risk loci through differential allelic expression analysis.

Sci Rep · 2024 · PMC11438911 · PMID 39341862

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highly significantno p-value reported
3 b,c), but we identified other highly significant daeQTLs (adjusted p-values smaller than 5.0E−04) for 2507 genes.

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