• TGFBI Gene Mutation Analysis
  • Anti Mullerian Hormone (AMH)
  • Meperidine, Urine
  • PML-RARA (Promyelocytic Leukemia/Retinoic Acid Receptor Alpha) Translocation, t(15;17) Analysis
  • Glucose, Body Fluid
  • Electrophoresis, Protein, 24 Hour, Urine
  • Cerebral arterial thrombosis
  • Phenobarbital, Serum
  • Chromosome Breakage Study, Tissue
  • HER2/neu (ERBB2), IHC, Semi-Quantitative, Other Tissue
  • LDS
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  • /Comprehensive Pharmacogenetics (PGx) Gene Variation Panel
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • LOINC
  • ICD10
  • Additional ICD10
  • References

Comprehensive Pharmacogenetics (PGx) Gene Variation Panel
Medical Test

Overview
Access to Comprehensive Pharmacogenetics (PGx) Gene Variation Panel is restricted.