Targeted Gene Sequencing in Children with Crohn's Disease and Their Parents: Implications for Missing Heritability.

G3 (Bethesda) · 2018 · PMC6118318 · PMID 30166421

Europe PMC DOI

hedged sentences

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closest p

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boldest claim

The sentences

marginally significantno p-value reported

For both models, we included R702W because of its widely reported association with Crohn’s disease, although the variant was marginally significant in this study.

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nominally significantno p-value reported

We identified three genes with nominally significant p-values: NOD2 , RTKN2 , and MGAT3 .

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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.