Barely Significant
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Causal inference for heritable phenotypic risk factors using heterogeneous genetic instruments.

PLoS Genet · 2021 · PMC8301661 · PMID 34157017

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highly significantno p-value reported
All five risk factors show highly significant effects, though multi-modality is detected in HDL-C and SBP.

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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.