• Hepatitis B Virus (HBV) by Molecular Method, Qualitative
  • Prenatal (Obstetrics) Carrier Screening for Inherited Genetic Conditions (Genesys Carrier Panel, LabCorp Inheritest®, UNITY Fetal Risk screen)
  • Tissue Transglutaminase (tTG) Antibody, IgG
  • Blood pH
  • Uniparental Disomy, FISH, Amniotic Fluid
  • CHIC2, 4q12 Deletion (FIP1L1 and PDGFRA Fusion), FISH, Blood
  • TNF receptor superfamily member 13B Gene Mutation Analysis
  • Eastern Equine Encephalitis Antibody, IgM by IFA, Serum
  • DKC1 Gene Mutation Analysis
  • Cholesterol, Body Fluid
  • LDS
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  • /Solute carrier family 6 member 2 (SLC6A2)
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  • Additional ICD10
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  • All
  • Diseases
  • Overview
  • Clinical Utility
  • Interpretation
  • Reference Ranges
  • Methodology
  • Specimen Collection
  • Additional Testing
  • Turnaround Time
  • CPT
  • ICD10
  • Additional ICD10
  • References

Solute carrier family 6 member 2 (SLC6A2)
Medical Test

Methodology
Access to Solute carrier family 6 member 2 (SLC6A2) is restricted.
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