Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000912538 | SCV001057648 | likely benign | not provided | 2022-02-22 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002505343 | SCV002800347 | likely benign | Brachydactyly type B1; Autosomal recessive Robinow syndrome | 2021-08-02 | criteria provided, single submitter | clinical testing |