Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genomic Research Center, |
RCV000714899 | SCV000845650 | likely pathogenic | Fanconi anemia complementation group A | 2018-08-07 | criteria provided, single submitter | clinical testing |