Barely Significant
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Family-based genome-wide association study of leprosy in Vietnam.

PLoS Pathog · 2020 · PMC7259797 · PMID 32421744

Europe PMCDOI
2
hedged sentences
0.0000
closest p · 0.0× alpha
0.0000
boldest claim

The sentences

highly significantp = 5.1x10 −14actually significant
The first, rs3764147, located on chromosome 13, is a missense variant (p.Ile254Val) of the LACC1 gene with a highly significant genome-wide p -value in the combined analysis of the discovery family and the replication case/control samples ( p = 5.1x10 −14 ).

also in 132,142 other papers

borderline non-significantno p-value reported
A borderline non-significant genome-wide p -value of 6.4x10 -8 was obtained for this SNP, with an OR of developing leprosy for AC vs.

also in 434 other papers

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.