Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003846386 | SCV004694878 | likely benign | Niemann-Pick disease, type C1 | 2023-11-11 | criteria provided, single submitter | clinical testing |