• Factor II (Prothrombin) Mutation
  • Ehrlichia chaffeensis Antibody, IgM
  • Chlamydophila pneumoniae DNA, Real-Time PCR, Qualitative
  • PM-1 (PM-Scl) Antibody
  • Lipoprotein Associated Phospholipase A2 Activity
  • Hexosaminidase A (HEXA) Gene Mutation Analysis
  • Bismuth, Urine
  • Schistosoma Exam, Urine
  • Bordetella pertussis Antibody, IgA, IgG
  • Butalbital, Serum
  • LDS
  • Sign up
  • Log in
  • LDS
  • /Medical Tests
  • /Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS
  • 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

Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS
Medical Test

Methodology
Access to Hereditary Colon Cancer Gene Mutation Panel (Lynch syndrome), NGS is restricted.