Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center For Human Genetics And Laboratory Diagnostics, |
RCV001002794 | SCV001160767 | likely pathogenic | Epilepsy, X-linked 1, with variable learning disabilities and behavior disorders | 2019-08-26 | criteria provided, single submitter | clinical testing |