Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Fulgent Genetics, |
RCV005045478 | SCV005672739 | likely pathogenic | Usher syndrome type 2C; Febrile seizures, familial, 4 | 2024-06-10 | criteria provided, single submitter | clinical testing |