Barely Significant
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Transcriptional regulation of the MET receptor tyrosine kinase gene by MeCP2 and sex-specific expression in autism and Rett syndrome.

Transl Psychiatry · 2013 · PMC3818007 · PMID 24150225

Europe PMCDOI
1
hedged sentence
0.0550
closest p · 1.1× alpha
0.0550
boldest claim

The sentences

approached significanceP =0.055so close (0.05 < p ≤ 0.1)
The interaction between rs1858830 allele and MECP2 mutation approached significance ( P =0.055).

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