Barely Significant
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Association Analysis of <i>WNT3</i>, <i>HLA-DRB5</i> and <i>IL1R2</i> Polymorphisms in Chinese Patients With Parkinson's Disease and Multiple System Atrophy.

Front Genet · 2021 · PMC8636743 · PMID 34868249

Europe PMCDOI
1
hedged sentence
0.0070
closest p · 0.1× alpha
0.0070
boldest claim

The sentences

highly significantp = 0.007actually significant
In addition, it became highly significant in the recessive model for the PD and LOPD group (OR: 1.331, 95% CI: 1.082–1.637, p = 0.007) ( Table 4 ).

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