Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV002463398 | SCV002757820 | uncertain significance | Orofaciodigital syndrome type 6; Joubert syndrome 17 | 2020-11-06 | criteria provided, single submitter | clinical testing |