Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001522617 | SCV001732192 | benign | Alagille syndrome due to a JAG1 point mutation | 2025-01-15 | criteria provided, single submitter | clinical testing |