Barely Significant
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Whole-exome sequencing identified genetic risk factors for asparaginase-related complications in childhood ALL patients.

Oncotarget · 2017 · PMC5546438 · PMID 28574850

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markedly significantno p-value reported
Our analysis also suggests that synergistic interactions might exist between the SNPs identified in each of the studied toxicities, which could explain the markedly significant associations and high odd-ratios in the combined SNPs models.

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