Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome- |
RCV001543315 | SCV001761860 | benign | Autosomal recessive Alport syndrome | 2021-07-10 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001712998 | SCV001946375 | benign | not provided | 2018-07-09 | criteria provided, single submitter | clinical testing |