Barely Significant
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Confirmation of GLRA3 as a susceptibility locus for albuminuria in Finnish patients with type 1 diabetes.

Sci Rep · 2018 · PMC6098108 · PMID 30120300

2
hedged sentences
0.0000
closest p · 0.0× alpha
0.0000
boldest claim

The sentences

highly significantp = 1.7 × 10 −9actually significant
While no association with AER was seen in the patients reaching the current recommended treatment target of an HbA 1c ≤ 7.0% (N = 304, β [95% CI] = −0.017 [−0.137–0.101], p = 0.78), the association was highly significant ( p = 1.7 × 10 −9 ) in the patients with an HbA 1c > 7.0% (N = 2560, β [95% CI] = 0.17 [0.117–0.230]).

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nominally significantno p-value reported
Despite substantial estimated heritability, only variants in the GLRA3 gene have been genome-wide significantly associated ( p -value < 5 × 10 −8 ) with diabetic albuminuria, in Finnish individuals with type 1 diabetes; However, replication attempt in non-Finnish Europeans with type 1 diabetes showed nominally significant association in the opposite direction, suggesting a population-specific effect, but simultaneously leaving the finding controversial.

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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.