Version 2.78

Basic Properties

OID
1.3.6.1.4.1.12009.10.1.2414
Name
MG_1_Genetic variant
Description
Genetic variant clinical significance
LOINCs using this list
1

Answer List

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

LOINC terms using this Answer List

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

LOINC Terminology Service (API) using HL7® FHIR® Get Info

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=LL377-3
ValueSet definition
https://fhir.loinc.org/ValueSet/?url=http://loinc.org/vs/LL377-3
ValueSet expansion
https://fhir.loinc.org/ValueSet/$expand?url=http://loinc.org/vs/LL377-3