Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Fulgent Genetics, |
RCV001029985 | SCV002786163 | uncertain significance | X-linked Alport syndrome | 2021-10-11 | criteria provided, single submitter | clinical testing | |
Bioscientia Institut fuer Medizinische Diagnostik Gmb |
RCV001029985 | SCV001192787 | uncertain significance | X-linked Alport syndrome | 2019-10-08 | no assertion criteria provided | clinical testing |