Barely Significant
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A comprehensive evaluation of the role of genetic variation in follicular lymphoma survival.

BMC Med Genet · 2014 · PMC4411784 · PMID 25294155

Europe PMCDOI
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hedged sentence
0.0500
closest p · 1.0× alpha
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boldest claim

The sentences

nominally significantp < 0.05actually significant
Among the 22 candidate SNPs evaluated, two imputed variants showed nominally significant association (p < 0.05) with lymphoma-specific death: rs1801131 in MTHFR (HR = 0.69, 95% CI 0.49-0.97, p = 0.03) and rs2069762 in IL2 (HR = 0.63, 95% CI 0.43-0.92, p = 0.02; Table 4 ). rs1801131 was also associated with lymphoma progression (HR = 0.59, 95% CI 0.45-0.77, p = 0.0001).

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