Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV002118118 | SCV002401545 | benign | not provided | 2023-12-21 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002486901 | SCV002803158 | benign | Brachydactyly type B1; Autosomal recessive Robinow syndrome | 2021-07-30 | criteria provided, single submitter | clinical testing |