Barely Significant
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Disease expression caused by different variants in the BEST1 gene: genotype and phenotype findings in bestrophinopathies.

Acta Ophthalmol · 2022 · PMC9328113 · PMID 34327816

1
hedged sentence
0.0600
closest p · 1.2× alpha
0.0600
boldest claim

The sentences

close to significancep = 0.06so close (0.05 < p ≤ 0.1)
The differences were close to significance (p = 0.06), with the median CRT increasing from stage 1 (261 μm) to stage 3 in BVMD (348 μm) and then decreasing to stage 5 (237 μm).

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