Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001220883 | SCV001392896 | likely benign | Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome | 2023-08-08 | criteria provided, single submitter | clinical testing | |
Sema4, |
RCV002258165 | SCV002530534 | uncertain significance | Hereditary cancer-predisposing syndrome | 2021-07-22 | criteria provided, single submitter | curation |