Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Molecular Genetics Laboratory, |
RCV000578363 | SCV000680101 | likely pathogenic | X-linked recessive seizure and neurodevelopmental deficit | 2017-07-03 | no assertion criteria provided | clinical testing |