Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Unit for Genetic & Epidemiological Research on Neurological Disorders, |
RCV000516067 | SCV000574462 | likely pathogenic | Hereditary spastic paraplegia | 2017-03-07 | criteria provided, single submitter | research | |
Paris Brain Institute, |
RCV001391460 | SCV001451232 | pathogenic | Hereditary spastic paraplegia 10 | criteria provided, single submitter | clinical testing |