| CLASS | MOLPATH.MISC | LP121011-3 |
| COMPONENT | Genetic variant clinical significance | LP62054-9 |
| PROPERTY | Imp | LP6819-9 |
| TIME_ASPCT | Pt | LP6960-1 |
| SYSTEM | Bld/Tiss | LP7061-7 |
| SCALE_TYP | Nom | LP7750-5 |
| METHOD_TYP | Molgen | LP6404-0 |
| AnswerList | MG_1_Genetic variant | LL377-3 |
| parent | Lab terms not yet categorized | LP248770-2 |
| CLASSTYPE | Laboratory class | |
| ORDER_OBS | Observation | |
| UNITSREQUIRED | N |
| LONG_COMMON_NAME | en-US | Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics method |
| LONG_COMMON_NAME | en-US | Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics method |
| SHORTNAME | en-US | Genetic variant clin sig Bld/T-Imp |
| ConsumerName | en-US | Genetic variant clinical significance, Blood or tissue specimen |
| SHORTNAME | pt-BR | Genetic variant clin sig Sg/T-Imp |
| LONG_COMMON_NAME | fr-FR | Variant génétique signification clinique [Interprétation] Sang/Tissu ; Résultat nominal ; Biologie moléculaire |
| LONG_COMMON_NAME | nl-NL | Genetische variant klinische significantie [interpretatie] in bloed of weefsel d.m.v. moleculair genetisch onderzoek |
| LONG_COMMON_NAME | es-MX | Importancia clínica de la variante genética: Sangre o tejido : Punto temporal: Impresión / interpretación del estudio: Nominal: Genética molecular |
LOINC Version: 2.77
FHIR