| CLASS | MOLPATH | LP7822-2 |
| COMPONENT | Genetic variant diagnostic significance | LP411468-4 |
| PROPERTY | Imp | LP6819-9 |
| TIME_ASPCT | Pt | LP6960-1 |
| SYSTEM | Bld/Tiss | LP7061-7 |
| SCALE_TYP | Nar | LP7749-7 |
| parent | Genetic variant diagnostic significance | Blood or Tissue | Molecular pathology | LP417054-6 |
| CLASSTYPE | Laboratory class | |
| ORDER_OBS | Observation |
| LONG_COMMON_NAME | en-US | Genetic variant diagnostic significance [Interpretation] in Blood or Tissue Narrative |
| LONG_COMMON_NAME | en-US | Genetic variant diagnostic significance [Interpretation] in Blood or Tissue Narrative |
| SHORTNAME | en-US | Genetic variant diag sig Bld/T-Imp |
| ConsumerName | en-US | Interpretation of Genetic variant diagnostic significance test result, Blood or tissue specimen |
| LONG_COMMON_NAME | fr-FR | Variant génétique influançant le diagnostic [Interprétation] Sang/Tissu ; Résultat textuel |
| LONG_COMMON_NAME | es-MX | Importancia diagnóstica de la variante genética: Sangre o tejido : Punto temporal: Impresión / interpretación del estudio: Narrativo: |
LOINC Version: 2.77
FHIR