Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001416628 | SCV001618811 | likely benign | Rett syndrome, congenital variant | 2023-12-06 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001537275 | SCV001754137 | likely benign | not provided | 2019-11-08 | criteria provided, single submitter | clinical testing |