| Answer | Pathogenic | LA6668-3 |
| Answer | Likely pathogenic | LA26332-9 |
| Answer | Uncertain significance | LA26333-7 |
| Answer | Likely benign | LA26334-5 |
| Answer | Benign | LA6675-8 |
| answers-for | Genetic variation clinical significance [Imp] | 53037-8 |
| STATUS | NotStated |
| LONG_COMMON_NAME | en-US | ACMG_Clinical significance of genetic variation |
LOINC Version: 2.81
FHIR