Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003810301 | SCV004609928 | likely benign | Familial aplasia of the vermis; Meckel-Gruber syndrome | 2023-11-07 | criteria provided, single submitter | clinical testing |