Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute Of Human Genetics Munich, |
RCV000995769 | SCV001150107 | likely pathogenic | Rett syndrome, congenital variant | 2019-08-07 | criteria provided, single submitter | clinical testing |