• Tumor Necrosis Factor Receptor-Associated Periodic Syndrome (TRAPS)
  • Hunter Syndrome (IDS) Gene Mutation Analysis
  • Angiosarcoma, MYC (8q24) Amplification, FISH, Tissue
  • Beta-amyloid Protein Ratio 1-42/1-40 (QUEST AD-Detectâ„¢, INNOTEST® B-AMYLOID), Plasma
  • Benign neoplasm, adrenal gland
  • Francisella tularensis Antibody, IgG, IgM
  • Venous Blood Gases
  • Hemosiderin Stain, Urine
  • Beta Thalassemia Genetic Testing
  • SMAD4 Germline Mutation Analysis
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /ATP binding cassette subfamily G member 2 (ABCG2) Genotyping
  • 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

ATP binding cassette subfamily G member 2 (ABCG2) Genotyping
Medical Test

Specimen Collection
Access to ATP binding cassette subfamily G member 2 (ABCG2) Genotyping is restricted.