Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001722570 | SCV000715063 | likely benign | not provided | 2021-03-10 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000915552 | SCV001060764 | likely benign | Hereditary sensory neuropathy-deafness-dementia syndrome | 2023-03-26 | criteria provided, single submitter | clinical testing |