Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000458199 | SCV000559124 | likely benign | Hereditary cancer-predisposing syndrome | 2023-11-02 | criteria provided, single submitter | clinical testing | |
Sema4, |
RCV002257748 | SCV002538452 | likely benign | Nijmegen breakage syndrome-like disorder | 2021-03-14 | criteria provided, single submitter | curation | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV003479133 | SCV004223594 | likely benign | not specified | 2023-11-09 | criteria provided, single submitter | clinical testing |