• Sinusitis
  • Lyme Disease (Borrelia burgdorferi) Confirmatory Testing
  • Heparin Antifactor Xa Assay
  • Paroxysmal nocturnal hemoglobinuria
  • Carcinoid syndrome
  • Glycogen storage disease type I (von Gierke disease)
  • Glanzmann thrombasthenia (hereditary familial thrombocytopenia)
  • Obstetric Panel
  • Factor B Complement Antigen
  • Beta-2 Adrenergic Receptor (ADRB2) Gene Variation
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /SMAD2 Gene Mutation Analysis
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References
  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

SMAD2 Gene Mutation Analysis
Medical Test

Interpretation
Access to SMAD2 Gene Mutation Analysis is restricted.