Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001704467 | SCV000530629 | likely benign | not provided | 2019-08-13 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000876892 | SCV001019527 | benign | Hereditary sensory neuropathy-deafness-dementia syndrome | 2023-12-18 | criteria provided, single submitter | clinical testing |