Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001365551 | SCV001561826 | uncertain significance | not provided | 2021-08-26 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002476668 | SCV002801388 | uncertain significance | Brachydactyly type B1; Autosomal recessive Robinow syndrome | 2022-02-09 | criteria provided, single submitter | clinical testing |