Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000904998 | SCV001049556 | likely benign | not provided | 2022-11-15 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002502685 | SCV002808112 | likely benign | Brachydactyly type B1; Autosomal recessive Robinow syndrome | 2021-12-12 | criteria provided, single submitter | clinical testing |