47997-2
Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics method
Genetic variant clinical significance, a impression in blood or tissue by Molgen, a nominal result.
- LOINC
- 47997-2
- Component
- Genetic variant clinical significance
- Specimen
- Blood or tissue (Bld/Tiss)
- Property
- Impression (Imp)
- Scale
- Nominal (Nom)
- Method
- Molgen
- Class
- MOLPATH.MISC
- Status
- ACTIVE