Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001463635 | SCV001667582 | likely benign | Familial aplasia of the vermis; Meckel-Gruber syndrome; Nephronophthisis | 2023-11-06 | criteria provided, single submitter | clinical testing | |
Natera, |
RCV001832602 | SCV002094190 | likely benign | Leber congenital amaurosis | 2021-08-09 | no assertion criteria provided | clinical testing |