Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001429287 | SCV001632001 | likely benign | Alagille syndrome due to a JAG1 point mutation | 2022-01-06 | criteria provided, single submitter | clinical testing |