Barely Significant
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Elucidation of the genetic causes of bicuspid aortic valve disease.

Cardiovasc Res · 2023 · PMC10153415 · PMID 35727948

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nominally significantP < 0.05actually significant
We applied LDSC to partition the SNP-based heritability for BAV across these 16 transcriptome profiles and found nominally significant GWAS enrichment ( P < 0.05) among 11 foetal cardiac cell types (see Supplementary material online , Table S3 ).

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