Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000672239 | SCV000797329 | likely pathogenic | Fanconi anemia complementation group A | 2018-01-23 | criteria provided, single submitter | clinical testing | |
Baylor Genetics | RCV000672239 | SCV004196633 | likely pathogenic | Fanconi anemia complementation group A | 2022-05-16 | criteria provided, single submitter | clinical testing |