Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome- |
RCV001527196 | SCV001738142 | likely benign | Autosomal recessive Alport syndrome | 2021-06-10 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001673111 | SCV001884934 | benign | not provided | 2018-07-09 | criteria provided, single submitter | clinical testing |