Barely Significant
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Genetic variants linked to myopic macular degeneration in persons with high myopia: CREAM Consortium.

PLoS One · 2019 · PMC6695159 · PMID 31415580

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highly significantno p-value reported
For two of the most highly significant SNPs first associated with refractive error ( GJD2 and RASGRF1 ), no association with MMD was found in an ethnically-homogenous Chinese population [ 31 ].

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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.