Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute Of Human Genetics Munich, |
RCV000995861 | SCV001150244 | likely pathogenic | Developmental and epileptic encephalopathy, 11 | 2019-01-07 | criteria provided, single submitter | clinical testing |