Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002217466 | SCV002370589 | likely benign | not provided | 2024-11-05 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002479885 | SCV002794798 | likely benign | Cataract 41; Wolfram syndrome 1; Autosomal dominant nonsyndromic hearing loss 6; Type 2 diabetes mellitus; Wolfram-like syndrome | 2022-03-04 | criteria provided, single submitter | clinical testing |