LL4034-6
ACMG_Clinical significance of genetic variation
Active
Basic Properties
- OID
- 1.3.6.1.4.1.12009.10.1.2644
- Name
- ACMG_Clinical significance of genetic variation
- Description
- Answers: 5; Scale: Ord; Code: -; Score: -
- LOINCs using this list
- 1
Answer List
| Answer | Code | Score | Answer ID |
|---|---|---|---|
| Pathogenic | LA6668-3 | ||
| Likely pathogenic | LA26332-9 | ||
| Uncertain significance | LA26333-7 | ||
| Likely benign | LA26334-5 | ||
| Benign | LA6675-8 |
LOINC terms using this Answer List
| 53037-8 | Genetic variation clinical significance [Imp] |
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/$lookup?system=http: //loinc.org&code=LL4034-6 - ValueSet definition
- https:
//fhir.loinc.org/ValueSet/?url=http: //loinc.org/vs/LL4034-6 - ValueSet expansion
- https:
//fhir.loinc.org/ValueSet/$expand?url=http: //loinc.org/vs/LL4034-6
LOINC Copyright
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