Barely Significant
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Coding Region Mutation Screening in Optineurin in Chinese Normal-Tension Glaucoma Patients.

Dis Markers · 2019 · PMC6526575 · PMID 31198474

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

The sentences

did not reach statistical significancep > 0.05actually significant
Out of these seven OPTN sequence variants, c.464G>A (T34T) was significantly associated with NTG in both the allelic and genotypic association analyses (allelic association: p = 0.0001, OR = 2.20, 95% CI: 1.46-3.31; genotypic association: p = 0.0001), whereas the association of other variants with NTG did not reach statistical significance ( p > 0.05).

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