Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV002240444 | SCV001673782 | likely benign | Osteogenesis imperfecta type I; Ehlers-Danlos syndrome, classic type, 1 | 2024-01-15 | criteria provided, single submitter | clinical testing | |
ARUP Laboratories, |
RCV001579559 | SCV004562483 | likely benign | not provided | 2023-09-11 | criteria provided, single submitter | clinical testing | |
Genome Diagnostics Laboratory, |
RCV001579559 | SCV001807677 | likely benign | not provided | no assertion criteria provided | clinical testing | ||
Clinical Genetics DNA and cytogenetics Diagnostics Lab, |
RCV001579559 | SCV001964439 | likely benign | not provided | no assertion criteria provided | clinical testing |