Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Blueprint Genetics | RCV000788762 | SCV000927997 | uncertain significance | not provided | 2018-10-17 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002535790 | SCV003321841 | likely benign | Osteogenesis imperfecta type I; Ehlers-Danlos syndrome, classic type, 1 | 2024-01-03 | criteria provided, single submitter | clinical testing |