Version 2.77

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

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