Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001703601 | SCV000518734 | likely benign | not provided | 2021-03-22 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV000869457 | SCV001010885 | likely benign | Rett syndrome, congenital variant | 2023-12-16 | criteria provided, single submitter | clinical testing |