Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000649383 | SCV000771210 | likely benign | Hereditary sensory neuropathy-deafness-dementia syndrome | 2023-02-22 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001592811 | SCV001814669 | likely benign | not provided | 2020-12-04 | criteria provided, single submitter | clinical testing | |
Ce |
RCV001592811 | SCV002063717 | likely benign | not provided | 2021-11-01 | criteria provided, single submitter | clinical testing |