Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute for Clinical Genetics, |
RCV003237459 | SCV002009235 | uncertain significance | not provided | 2021-11-03 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV001761807 | SCV002776510 | uncertain significance | Fanconi anemia complementation group P | 2021-11-17 | criteria provided, single submitter | clinical testing |