Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000559872 | SCV000628240 | likely benign | Hereditary cancer-predisposing syndrome | 2023-10-29 | criteria provided, single submitter | clinical testing | |
Mendelics | RCV000987600 | SCV001136978 | likely benign | Nijmegen breakage syndrome-like disorder | 2019-05-28 | criteria provided, single submitter | clinical testing |