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

AnswerCodeScoreAnswer ID
PathogenicLA6668-3
Presumed PathogenicLA6669-1
Novel Presumed PathogenicLA6670-9
Novel Unknown SignificanceLA6671-7
Novel Presumed BenignLA6672-5
NovelLA6673-3
Presumed BenignLA6674-1
BenignLA6675-8
ResistantLA6676-6
ResponsiveLA6677-4
Novel Presumed Non-ResponsiveLA6678-2
Novel Presumed ResponsiveLA6679-0
UnclassifiedLA6680-8
PolymorphismLA6681-6
Unknown SignificanceLA6682-4

LOINC terms using this Answer List

47997-2Genetic 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