Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001720166 | SCV000522969 | likely benign | not provided | 2020-06-02 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000939547 | SCV001085393 | likely benign | Hereditary sensory neuropathy-deafness-dementia syndrome | 2024-01-11 | criteria provided, single submitter | clinical testing |