Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute for Clinical Genetics, |
RCV003238702 | SCV002009101 | uncertain significance | not provided | 2021-11-03 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV001761758 | SCV002782213 | uncertain significance | Fanconi anemia complementation group D2 | 2021-12-20 | criteria provided, single submitter | clinical testing |