Barely Significant
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Comorbidity of Novel <i>CRHR2</i> Gene Variants in Type 2 Diabetes and Depression.

Int J Mol Sci · 2022 · PMC9456299 · PMID 36077219

Europe PMCDOI
1
hedged sentence
0.0400
closest p · 0.8× alpha
0.0400
boldest claim

The sentences

borderline significancep = 0.04actually significant
A rare CRHR2 variant (rs3779250-risk allele-C) has been reported in Japanese patients with MDD [ 21 ], and a previous study in Belgium reported an MDD-risk variant with borderline significance ( p = 0.04) [ 54 ].

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