Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV002220621 | SCV002363393 | likely benign | Smith-Lemli-Opitz syndrome | 2022-02-04 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002220621 | SCV002809638 | likely benign | Smith-Lemli-Opitz syndrome | 2022-04-07 | criteria provided, single submitter | clinical testing |