Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001538361 | SCV001756000 | benign | not provided | 2019-09-25 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001785824 | SCV002026879 | benign | Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1 | 2021-09-05 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001785825 | SCV002026880 | benign | Lateral meningocele syndrome | 2021-09-05 | criteria provided, single submitter | clinical testing |