Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute Of Human Genetics Munich, |
RCV001254069 | SCV001429982 | likely pathogenic | Autosomal dominant cerebellar ataxia, deafness and narcolepsy | 2020-06-08 | criteria provided, single submitter | clinical testing |