A missense mutation in <i>TCN2</i> is associated with decreased risk for congenital heart defects and may increase cellular uptake of vitamin B12 via Megalin.

Oncotarget · 2017 · PMC5589654 · PMID 28903415

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hedged sentence

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closest p

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boldest claim

The sentences

nominally significantno p-value reported

Moreover, the c.230A>T is a specific polymorphism in East-Asian populations and exhibits nominally significant evidence for positive selection in Northern Chinese populations.

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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.