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