Barely Significant
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A rare sequence variant in intron 1 of THAP1 is associated with primary dystonia.

Mol Genet Genomic Med · 2014 · PMC4049367 · PMID 24936516

Europe PMCDOI
1
hedged sentence
0.1300
closest p · 2.6× alpha
0.1300
boldest claim

The sentences

did not reach statistical significanceP = 0.13not close (p > 0.1)
However, the difference in MAF did not reach statistical significance when compared with the EVS database ( P = 0.13).

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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.