Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center For Human Genetics And Laboratory Diagnostics, |
RCV001258332 | SCV001435298 | pathogenic | Rett syndrome, congenital variant | 2020-07-03 | criteria provided, single submitter | clinical testing |