Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV002179412 | SCV002339792 | likely benign | not provided | 2023-11-27 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002494038 | SCV002802902 | likely benign | Brachydactyly type B1; Autosomal recessive Robinow syndrome | 2021-12-15 | criteria provided, single submitter | clinical testing |