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. 2022 Apr 30;12(5):733. doi: 10.3390/jpm12050733
gnomAD Genome Aggregation Database
HCM hypertrophic cardiomyopathy
LP/P likely pathogenic/pathogenic
LVH left ventricular hypertrophy
LVNC left ventricular non-compaction
VUS variant of uncertain significance
ES exome sequencing
S:N signal-to-noise
ACMG American College of Medical Genetics