Barely Significant
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Copy number variants in candidate genes are genetic modifiers of Hirschsprung disease.

PLoS One · 2011 · PMC3119685 · PMID 21712996

Europe PMCDOI
1
hedged sentence
0.0029
closest p · 0.1× alpha
0.0029
boldest claim

The sentences

highly significantP = 0.0029actually significant
This association is highly significant since the 10 isolated HSCR patients have only one variant but the 8 HSCR cases with additional anomalies have 7 variants (P = 0.0029).

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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.