Barely Significant
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Genetic Variants and Their Associations to Type 2 Diabetes Mellitus Complications in the United Arab Emirates.

Front Endocrinol (Lausanne) · 2021 · PMC8772337 · PMID 35069435

2
hedged sentences
0.0100
closest p · 0.2× alpha
0.0100
boldest claim

The sentences

borderline significantp-value < 0.01actually significant
In the case of DNp, rs743507 and rs1808593 (p-value= 0.004) in the NOS3 gene were found to be as borderline significant (p-value < 0.01).

also in 11,409 other papers

highly significantno p-value reported
Dyslipidemia was present in all patients with complications and in 69% of the no complications group, making it a highly significant cofactor in disease progression.

also in 132,142 other papers

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.