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. 2026 Jul 11;48(7):706. doi: 10.3390/cimb48070706
ACMG American College of Medical Genetics and Genomics
AI Artificial intelligence
ES Exome sequencing
HPO Human Phenotype Ontology
SNV Single-nucleotide variant
UP2 Universal Pathogenicity Predictor
VUS Variant of uncertain significance
WGS Whole-genome sequencing