Barely Significant
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Identification of genetic variation that determines human trehalase activity and its association with type 2 diabetes.

Hum Genet · 2013 · PMC3654185 · PMID 23468175

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nominally significantno p-value reported
In subsequent association mapping studies, several SNPs with nominally significant associations with T2D are mapped to or near TREH, UBASH3B, KIRREL3 and SNX19.

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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.