Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001501956 | SCV001706778 | likely benign | Ehlers-Danlos syndrome, type 4 | 2019-04-05 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV001501956 | SCV004830127 | likely benign | Ehlers-Danlos syndrome, type 4 | 2023-10-02 | criteria provided, single submitter | clinical testing |