Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000670328 | SCV000795168 | uncertain significance | Autosomal recessive Alport syndrome | 2017-10-30 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002532100 | SCV003467279 | likely benign | not provided | 2023-12-20 | criteria provided, single submitter | clinical testing |