Barely Significant
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<i>C6orf10</i> Low-Frequency and Rare Variants in Italian Multiple Sclerosis Patients.

Front Genet · 2019 · PMC6607989 · PMID 31297130

Europe PMCDOI
1
hedged sentence
0.0010
closest p · 0.0× alpha
0.0010
boldest claim

The sentences

highly significantp -value < 0.001actually significant
Based on frequencies in the Control gnomAD, the OR for the rs1687005 risk T-allele was 4.57 (95% CI 2.33–8.97) and the odds ratios for the rs12722600 risk T-allele was 9.88 (95% CI 5.71–17.09), both highly significant ( p -value < 0.001).

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