Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001718933 | SCV000721849 | benign | not provided | 2020-08-14 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000873962 | SCV001016065 | likely benign | Hereditary sensory neuropathy-deafness-dementia syndrome | 2023-12-23 | criteria provided, single submitter | clinical testing |