Barely Significant
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Genetics of skin color variation in Europeans: genome-wide association studies with functional follow-up.

Hum Genet · 2015 · PMC4495261 · PMID 25963972

Europe PMCDOI
1
hedged sentence
0.0500
closest p · 1.0× alpha
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boldest claim

The sentences

nominally significantp value <0.05actually significant
BNC2 rs10756819 was not genome-wide significant but showed a consistent and nominally significant effect in all studied cohorts ( p value <0.05); this therefore replicated our previous finding from a candidate gene study (Jacobs et al. 2012 ) suggesting that BNC2 influences subtle variation in skin color.

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