Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Fulgent Genetics, |
RCV000791325 | SCV002777213 | likely pathogenic | X-linked Alport syndrome | 2022-01-03 | criteria provided, single submitter | clinical testing | |
Institute of Human Genetics, |
RCV000791325 | SCV000930023 | likely pathogenic | X-linked Alport syndrome | no assertion criteria provided | clinical testing |