Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000670944 | SCV000795868 | likely benign | Autosomal recessive Alport syndrome | 2017-11-21 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001491093 | SCV001695677 | likely benign | not provided | 2023-12-26 | criteria provided, single submitter | clinical testing |