Barely Significant
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Whole-exome sequencing of BRCA-negative breast cancer patients and case-control analyses identify variants associated with breast cancer susceptibility.

Hum Genomics · 2022 · PMC9685974 · PMID 36424660

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Of these 34 variants, 26 were significantly enriched in phs000822.v1.p1 when compared against gnomAD (EAS) while eight did not reach statistical significance.

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