Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Fulgent Genetics, |
RCV002499492 | SCV002799394 | likely pathogenic | Autosomal recessive Alport syndrome; Benign familial hematuria | 2022-02-15 | criteria provided, single submitter | clinical testing | |
Bioscientia Institut fuer Medizinische Diagnostik Gmb |
RCV001280874 | SCV001468219 | likely pathogenic | Benign familial hematuria | 2020-02-06 | no assertion criteria provided | clinical testing |