Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome- |
RCV001527193 | SCV001738139 | benign | Autosomal recessive Alport syndrome | 2021-06-10 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001655795 | SCV001865957 | benign | not provided | 2018-06-22 | criteria provided, single submitter | clinical testing |