Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Clinical Genetics laboratory, |
RCV000767219 | SCV000897613 | uncertain significance | Charcot-Marie-Tooth disease, axonal, type 2O | 2019-03-29 | no assertion criteria provided | clinical testing |