53037-8
Genetic variation clinical significance [Imp]
Genetic disease sequence variation interpretation, a impression in blood or tissue by Molgen, a nominal result.
- LOINC
- 53037-8
- Component
- Genetic disease sequence variation interpretation
- Specimen
- Blood or tissue (Bld/Tiss)
- Property
- Impression (Imp)
- Scale
- Nominal (Nom)
- Method
- Molgen
- Class
- HL7.GENETICS
- Status
- ACTIVE