• Zopiclone, Urine
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  • Prader-Willi and Angelman Syndrome Molecular Analysis
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  • Hemosiderin Stain, Urine
  • Salivary Gland Tumor, MYB (6q23) Rearrangement by FISH
  • Methanol
  • Vanadium, Serum
  • Phospholipase C Gamma 2 (PLCG2) Gene Mutation Analysis
  • Glycogen storage disease type II (Pompe disease)
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  • /Cytochrome P450 3A7 (CYP3A7) Genotyping
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  • 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

Cytochrome P450 3A7 (CYP3A7) Genotyping
Medical Test

Methodology
Access to Cytochrome P450 3A7 (CYP3A7) Genotyping is restricted.