A spotter's guide to SNPtic exons: The common splice variants underlying some SNP-phenotype correlations.

Mol Genet Genomic Med · 2022 · PMC8801146 · PMID 34708937

Europe PMC DOI

hedged sentence

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closest p

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boldest claim

The sentences

probable significanceno p-value reported

For Google results, we considered as ‘hits’ only those results that originated from peer‐reviewed literature in which the SNP was described as being of probable significance to a particular phenotype.

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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.