Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center of Excellence for Medical Genomics, |
RCV002281627 | SCV002570079 | likely pathogenic | Multiple congenital anomalies-hypotonia-seizures syndrome 2 | 2002-09-08 | no assertion criteria provided | research |