Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV005085396 | SCV005715714 | benign | Alagille syndrome due to a JAG1 point mutation | 2024-03-13 | criteria provided, single submitter | clinical testing |