Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genetic Diseases Diagnostic Center, |
RCV000786061 | SCV000864392 | likely pathogenic | Hereditary spastic paraplegia 35 | 2018-12-18 | no assertion criteria provided | clinical testing |