Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001497686 | SCV001702422 | likely benign | Familial aplasia of the vermis; Meckel-Gruber syndrome; Nephronophthisis | 2024-01-25 | criteria provided, single submitter | clinical testing | |
Breakthrough Genomics, |
RCV004706225 | SCV005216208 | likely benign | not provided | criteria provided, single submitter | not provided |