Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV001727283 | SCV001962559 | likely benign | not provided | 2021-07-01 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002496051 | SCV002801974 | likely benign | Cataract 41; Wolfram syndrome 1; Autosomal dominant nonsyndromic hearing loss 6; Type 2 diabetes mellitus; Wolfram-like syndrome | 2021-08-16 | criteria provided, single submitter | clinical testing |