Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001477796 | SCV001682047 | likely benign | Hereditary cancer-predisposing syndrome | 2018-08-22 | criteria provided, single submitter | clinical testing | |
Sema4, |
RCV002258068 | SCV002538510 | uncertain significance | Nijmegen breakage syndrome-like disorder | 2022-01-02 | criteria provided, single submitter | curation | |
Women's Health and Genetics/Laboratory Corporation of America, |
RCV003479252 | SCV004223812 | likely benign | not specified | 2023-11-14 | criteria provided, single submitter | clinical testing |