Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center for Human Genetics, |
RCV000659487 | SCV000781303 | uncertain significance | Ehlers-Danlos syndrome, classic type | 2016-11-01 | criteria provided, single submitter | clinical testing |