Barely Significant
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Genetic polymorphisms associated with increased risk of developing chronic myelogenous leukemia.

Oncotarget · 2015 · PMC4742176 · PMID 26474455

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highly significantno p-value reported
In conclusion this study highlights the pertinence of highly significant risk alleles identified in 437 CML patients out of 16 561 SNPs, and also provides a rationale for evaluating implicated genes for their potential role in CML development.

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