Barely Significant
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A decision algorithm to identify patients with high probability of monogenic diabetes due to HNF1A mutations.

Endocrine · 2019 · PMC6453873 · PMID 30778899

1
hedged sentence
0.1400
closest p · 2.8× alpha
0.1400
boldest claim

The sentences

did not reach statistical significancep = 0.14not close (p > 0.1)
The adjusted difference between HNF1A MODY and type 1 diabetes did not reach statistical significance (1.1 μg/ml, p = 0.14).

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