Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome- |
RCV001527253 | SCV001738211 | benign | Autosomal recessive Alport syndrome | 2021-06-10 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001638121 | SCV001851137 | benign | not provided | 2018-06-22 | criteria provided, single submitter | clinical testing |