Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Revvity Omics, |
RCV001449976 | SCV002020142 | likely pathogenic | Niemann-Pick disease, type C1 | 2021-04-05 | criteria provided, single submitter | clinical testing | |
Hereditary Research Laboratory, |
RCV001449976 | SCV001653518 | pathogenic | Niemann-Pick disease, type C1 | 2021-06-02 | no assertion criteria provided | clinical testing |