Genome-wide association study of primary open angle glaucoma risk and quantitative traits.

Mol Vis · 2012 · PMC3351427 · PMID 22605921

Europe PMC

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highly significantno p-value reported

Discussion We report two SNPs highly significant in our discovery data for the phenotypes CCT and CDR.

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nominally significantno p-value reported

We found 4 nominally significant results in the replication cohort, but none passed correction for multiple testing.

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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.