Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000546418 | SCV000626449 | likely benign | Fanconi anemia | 2024-01-27 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002490953 | SCV002804114 | likely benign | Fanconi anemia complementation group P | 2022-03-23 | criteria provided, single submitter | clinical testing |