LL377-3
MG_1_Genetic variant
Active
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
Requests to this service require a free LOINC username and password. Below is a sample of the possible capabilities. See the LOINC Terminology Service documentation for more information.
- 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
LOINC Copyright
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