Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001698182 | SCV000531137 | likely benign | not provided | 2018-05-04 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000865374 | SCV001006327 | benign | Osteogenesis imperfecta type I; Ehlers-Danlos syndrome, classic type, 1 | 2024-01-25 | criteria provided, single submitter | clinical testing | |
ARUP Laboratories, |
RCV001698182 | SCV001471775 | benign | not provided | 2022-04-28 | criteria provided, single submitter | clinical testing |