Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Mendelics | RCV002249493 | SCV002516350 | likely pathogenic | Charcot-Marie-Tooth disease X-linked dominant 1 | 2022-05-04 | criteria provided, single submitter | clinical testing | |
Inherited Neuropathy Consortium | RCV000789795 | SCV000929179 | uncertain significance | Charcot-Marie-Tooth disease | no assertion criteria provided | literature only |