Barely Significant
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Linkage disequilibrium mapping of CHEK2: common variation and breast cancer risk.

PLoS Med · 2006 · PMC1457009 · PMID 16671833

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marginally significantno p-value reported
The 1100delC was exclusively carried on rare haplotypes, which may explain the marginally significant association between the group of 19 rare haplotypes and breast cancer risk ( Table 4 ).

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