Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001698201 | SCV000526506 | likely benign | not provided | 2020-11-10 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000897597 | SCV001041751 | likely benign | Intellectual disability, autosomal dominant 8 | 2024-01-21 | criteria provided, single submitter | clinical testing |