Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Fulgent Genetics, |
RCV002477795 | SCV002778779 | uncertain significance | Focal segmental glomerulosclerosis 5; Charcot-Marie-Tooth disease dominant intermediate E | 2021-10-29 | criteria provided, single submitter | clinical testing | |
Inherited Neuropathy Consortium | RCV000789984 | SCV000929373 | uncertain significance | Charcot-Marie-Tooth disease | no assertion criteria provided | literature only |