Barely Significant
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Association and mutation analyses of 16p11.2 autism candidate genes.

PLoS One · 2009 · PMC2644762 · PMID 19242545

Europe PMCDOI
1
hedged sentence
0.0490
closest p · 1.0× alpha
0.0490
boldest claim

The sentences

nominally significantp = 0.049actually significant
The TDT identified one nominally significant association (p = 0.049) with intragenic marker rs7193756 (chr16:29,657,155-29,657,655) from the Affymetrix 5.0 data; however, the DFAM was not significant (p = 0.20) ( Table S1 ).

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