Barely Significant
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Whole-exome and whole-genome sequencing of 1064 individuals with type 1 diabetes reveals novel genes for diabetic kidney disease.

Diabetologia · 2024 · PMC11519100 · PMID 39103720

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nominally significantp <0.05actually significant
Furthermore, for the single variants within these genes that were nominally significant ( p <0.05) in the FinnDiane WES/WGS meta-analysis, we tested for replication in the FinnDiane, THL Biobank, FinnGen GWAS and TOPMed WGS data.

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