LOINC
Version 2.71

47997-2Genetic variant clinical significance [Interpretation] in Blood or Tissue by Molecular genetics methodActive

Fully-Specified Name

Component
Genetic variant clinical significance
Property
Imp
Time
Pt
System
Bld/Tiss
Scale
Nom
Method
Molgen

Additional Names

Short Name
Genetic variant clin sig Bld/T-Imp
Display Name
Genetic variant clinical significance Molgen (Bld/Tiss) [Interp]
Consumer Name Alpha
Genetic variant clinical significance, Blood or tissue specimen

Normative Answer List LL377-3

Answer Code Score Answer ID
Pathogenic LA6668-3
Presumed Pathogenic LA6669-1
Novel Presumed Pathogenic LA6670-9
Novel Unknown Significance LA6671-7
Novel Presumed Benign LA6672-5
Novel LA6673-3
Presumed Benign LA6674-1
Benign LA6675-8
Resistant LA6676-6
Responsive LA6677-4
Novel Presumed Non-Responsive LA6678-2
Novel Presumed Responsive LA6679-0
Unclassified LA6680-8
Polymorphism LA6681-6
Unknown Significance LA6682-4

Basic Attributes

Class
MOLPATH.MISC
Type
Laboratory
First Released
Version 2.21
Last Updated
Version 2.26
Order vs. Observation
Observation

Member of these Panels

LOINC Long Common Name
48014-5 Sequence variation panel - Blood or Tissue by Molecular genetics method

Language Variants Get Info

zh-CNChinese (China)
遗传变异临床意义:印象:时间点:全血/组织:名义型:分子遗传学类实验室方法
nl-NLDutch (Netherlands)
genetische variant klinische significantie:interpretatie:moment:bloed of weefsel:nominaal:moleculair genetisch onderzoek
fr-FRFrench (France)
Variant génétique signification clinique:Interprétation:Ponctuel:Sang/Tissu:Résultat nominal:Biologie moléculaire
it-ITItalian (Italy)
Variante genetica, significato clinico:Imp:Pt:Sangue/Tess:Nom:Molgen
pt-BRPortuguese (Brazil)
Significado da variação genética clínica:Imp:Pt:Sg/Tecido:Nom:Genética molecular
ru-RURussian (Russian Federation)
Генетический вариант клиническая значимость:Впчт:ТчкВрм:Кр/Тк:Ном:МолГен
es-ESSpanish (Spain)
Significado clínico de variante genética:Impresión/interpretación del estudio:Punto temporal:Sangre o tejido:Nom:Genética molecular
tr-TRTurkish (Turkey)
Genetik varyant klinik anlamlılık:İzlnm:Zmlı:Kan/Dk:Snf:Molgen

LOINC FHIR® API Example - CodeSystem Request Get Info

https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=47997-2