Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000866891 | SCV000713863 | benign | not provided | 2021-06-23 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV001406334 | SCV001608284 | likely benign | Rett syndrome, congenital variant | 2023-11-27 | criteria provided, single submitter | clinical testing |