Barely Significant
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Characterization of prevalent genetic variants in the Estonian Biobank body-mass index GWAS.

Nat Commun · 2025 · PMC12508233 · PMID 41062462

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nominally significantno p-value reported
All the lead variants from these loci showed at least nominally significant association in the latest available data freeze from the publicly available FinnGen dataset (freeze version 10) for the ‘Body-mass index, inverse-rank normalized’ trait, suggesting that these single nucleotide variants (SNVs) represent valid hits (Supplementary Fig. 4 ).

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