Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000412431 | SCV000485353 | likely pathogenic | Fanconi anemia complementation group C | 2015-11-24 | criteria provided, single submitter | clinical testing | |
Baylor Genetics | RCV000412431 | SCV004196688 | likely pathogenic | Fanconi anemia complementation group C | 2023-01-31 | criteria provided, single submitter | clinical testing |