Barely Significant
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Validations of Top and Novel Susceptibility Variants in All-Age Chinese Patients With Acute Lymphoblastic Leukemia.

Front Genet · 2020 · PMC7477633 · PMID 33193587

1
hedged sentence
0.0900
closest p · 1.8× alpha
0.0900
boldest claim

The sentences

only marginally significantP = 0.09so close (0.05 < p ≤ 0.1)
Particularly, we focused on the novel Hispanic-specific ALL risk signal at ERG locus, observing only marginally significant association of this SNP with ALL susceptibility in childhood patients [ P = 0.09, OR = 1.17 (0.98–1.40)], but not adults ( P = 0.76).

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