Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000671111 | SCV000796056 | likely pathogenic | Fanconi anemia complementation group A | 2017-11-28 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV000671111 | SCV002811639 | likely pathogenic | Fanconi anemia complementation group A | 2022-01-14 | criteria provided, single submitter | clinical testing |