Barely Significant
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Genotype Phenotype Correlation in Dent Disease 2 and Review of the Literature: <i>OCRL</i> Gene Pleiotropism or Extreme Phenotypic Variability of Lowe Syndrome?

Genes (Basel) · 2021 · PMC8535715 · PMID 34680992

Europe PMCDOI
1
hedged sentence
0.0500
closest p · 1.0× alpha
0.0500
boldest claim

The sentences

near significancep = 0.05actually significant
No significant difference in the frequency of extra-renal signs was observed except for a near significance ( p = 0.05) of ocular symptoms for non-truncating vs. truncating mutations ( Figure 5 ).

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