Barely Significant
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<i>FGFR4</i> c.1162G > A (p.Gly388Arg) Polymorphism Analysis in Turkish Patients with Retinoblastoma.

J Oncol · 2020 · PMC7787726 · PMID 33456465

Europe PMCDOI
1
hedged sentence
0.0700
closest p · 1.4× alpha
0.0700
boldest claim

The sentences

nearly significantp =0.07so close (0.05 < p ≤ 0.1)
In 19 (61.3%) of these patients, the FGFR4 p.Gly388Arg variant was identified ( p =0.07 is nearly significant).

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