Barely Significant
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Replication and predictive value of SNPs associated with melanoma and pigmentation traits in a Southern European case-control study.

PLoS One · 2013 · PMC3564929 · PMID 23393597

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

The sentences

nominally significantp<0.05actually significant
More specifically, the 34 selected variants from MelGene were distinguished in two groups: 1) all variants associated with melanoma at a level of p<0.05 following meta-analysis of relevant data from at least 3 independent case-control datasets (28 variants) and 2) additional biologically plausible variants representing potential causal pathways and selected from GWAS (3 variants) and candidate gene studies (3 variants) with genome-wide (p<10 −7 ) or nominally significant (p<0.05) associations.

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