Barely Significant
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A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study.

Breast Cancer Res · 2012 · PMC3446390 · PMID 22452962

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marginally significantno p-value reported
SNP rs13393577 and three more SNPs (3q26.32 rs3806685, 6q25.1 rs9498283, and 17q24.3 rs11077488) showing marginally significant associations in stage II ( P trend < 0.10) were further evaluated in stage III, which included 1,997 cases and 1,676 controls.

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