Barely Significant
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Human genetics of metabolic dysfunction-associated steatotic liver disease: from variants to cause to precision treatment.

J Clin Invest · 2025 · PMC11957700 · PMID 40166930

Europe PMCDOI
1
hedged sentence
0.0500
closest p · 1.0× alpha
0.0500
boldest claim

The sentences

nominally significantP < 0.05actually significant
Another NASH CRN study also found nominally significant ( P < 0.05) associations between PNPLA3 genotype and fibrosis or lobular inflammation ( 57 ).

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