Barely Significant
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A common variant of CNTNAP2 is associated with sub-threshold autistic traits and intellectual disability.

PLoS One · 2021 · PMC8668106 · PMID 34898614

Europe PMCDOI
1
hedged sentence
0.5200
closest p · 10.4× alpha
0.5200
boldest claim

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did not reach statistical significancep = 0 . 52not close (p > 0.1)
Post-hoc analysis demonstrated that this effect was larger in the TD group, although it did not reach statistical significance [t(55) = 1.98, p = 0 . 52 ].

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