Barely Significant
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Multi-ethnic distribution of clinically relevant CYP2C genotypes and haplotypes.

Pharmacogenomics J · 2013 · PMC3396745 · PMID 22491019

Europe PMCDOI
1
hedged sentence
0.0001
closest p · 0.0× alpha
0.0001
boldest claim

The sentences

highly significantp <0.0001actually significant
The overall across-population difference in CYP2C8 allele frequencies was highly significant for three polymorphic variants (rs11572080 [* 3 ], rs11572103 [* 2 ], rs10509681 [* 3 ]; p <0.0001).

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