Barely Significant
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Genome-Wide Association Meta-Analysis of Single-Nucleotide Polymorphisms and Symptomatic Venous Thromboembolism during Therapy for Acute Lymphoblastic Leukemia and Lymphoma in Caucasian Children.

Cancers (Basel) · 2020 · PMC7280960 · PMID 32438682

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borderline significantno p-value reported
A candidate SNP analysis of the NOPHO cohort identified a significant association between VTE and F11 rs2036914 (hazard ratio (HR) 1.52, 95%CI 1.11–2.07), a borderline significant association with FGG rs2066865 (HR 1.37, 95%CI 0.99–1.91) but no association with either ABO rs8176719 or F5 rs6025 [ 17 ].

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