Barely Significant
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SET Domain Containing 2 Deficiency in Myelodysplastic Syndrome.

Front Genet · 2020 · PMC7423969 · PMID 32849799

Europe PMCDOI
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hedged sentence
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closest p · 1.0× alpha
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The sentences

borderline significanceP = 0.05actually significant
However, SETD2 mutations/variants were of only borderline significance on univariate analysis ( P = 0.05).

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