Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001698143 | SCV000525828 | benign | not provided | 2019-07-22 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000873521 | SCV001015526 | benign | Hereditary sensory neuropathy-deafness-dementia syndrome | 2024-01-19 | criteria provided, single submitter | clinical testing | |
ARUP Laboratories, |
RCV001698143 | SCV002048110 | benign | not provided | 2023-09-22 | criteria provided, single submitter | clinical testing |