Barely Significant
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Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population.

Am J Hum Genet · 2019 · PMC6848996 · PMID 31607426

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nominally significantno p-value reported
While we find a nominally significant association between UPD of chromosome 22 and autism risk, we do not find significant associations between UPD and deleterious traits in the 23andMe database.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.