Barely Significant
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Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.

PLoS Genet · 2012 · PMC3343074 · PMID 22570617

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The sentences

nominally significantno p-value reported
A single-allele p-value of <0.05 was considered to be nominally significant and included in the PARIS analysis.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.