LOINC
Version 2.69

LL4034-6ACMG_Clinical significance of genetic variation / Answers: 5; Scale: Ord; Code: -; Score: -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: -
Externally Defined
False
Answers Shown
5
LOINCs Using This List
1
Source Name
American College of Medical Genetics

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 FHIR® API Examples - CodeSystem and ValueSet Requests Get Info

https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=LL4034-6 https://fhir.loinc.org/ValueSet/?url=http://loinc.org/vs/LL4034-6

LOINC Terms That Use This Answer List

53037-8 Genetic variation clinical significance [Imp]