Barely Significant
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Phenotypic severity of homozygous GCK mutations causing neonatal or childhood-onset diabetes is primarily mediated through effects on protein stability.

Hum Mol Genet · 2014 · PMC4240195 · PMID 25015100

Europe PMCDOI
1
hedged sentence
0.0020
closest p · 0.0× alpha
0.0020
boldest claim

The sentences

highly significantP = 0.002actually significant
Comparison of CSG with RSI detected a highly significant correlation ( r 2 = 0.74, P = 0.002).

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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.