Clinical Genomic Interpretation Service

Professional evaluation and explanation of genomic test results by qualified clinical geneticists or molecular pathologists to guide diagnosis, treatment, and risk assessment.

This fee covers the professional clinical interpretation of raw or analyzed genetic test data by qualified healthcare providers (e.g., certified genetic counselors, clinical molecular geneticists, or medical geneticists). Primary uses include translating variant classifications (e.g., pathogenic, VUS, benign) into patient-specific risk assessments; correlating findings with personal/family history; guiding diagnosis, surveillance, treatment (e.g., targeted therapy eligibility), reproductive planning, and cascade testing; generating structured, actionable reports compliant with ACMG/AMP guidelines; and supporting informed consent and post-test counseling.