Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000605049 | SCV000718419 | likely benign | not provided | 2019-06-05 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001050499 | SCV001214609 | likely benign | Intellectual disability, autosomal dominant 8 | 2023-11-10 | criteria provided, single submitter | clinical testing |