Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000975573 | SCV001123459 | likely benign | not provided | 2023-05-02 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002489430 | SCV002795389 | likely benign | Autosomal dominant Alport syndrome; Autosomal recessive Alport syndrome; Benign familial hematuria | 2021-07-19 | criteria provided, single submitter | clinical testing |