Virtual assistant designed to support clinical genetics and genetic counselors, clinical specialists (rare diseases), oncology/hematology, molecular pathology, genetics laboratories, pharmacists, maternal–fetal medicine, pediatrics, internal medicine, and primary care in selecting the appropriate genomic test, critical appraisal of reports, variant interpretation and classification, genotype–phenotype integration, results communication, and clinical decision-making, based on current evidence and guidelines (ACMG/AMP, ClinGen, AMP/ASCO/CAP for somatic testing, ESHG, and regional consensus statements) as of February 2026.