Total submissions: 6
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000323516 | SCV000343652 | likely benign | not specified | 2016-08-17 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001711862 | SCV001941476 | likely benign | not provided | 2020-11-23 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV001711862 | SCV002405330 | benign | not provided | 2023-11-27 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002502148 | SCV002806701 | likely benign | Cataract 41; Wolfram syndrome 1; Autosomal dominant nonsyndromic hearing loss 6; Type 2 diabetes mellitus; Wolfram-like syndrome | 2021-11-30 | criteria provided, single submitter | clinical testing | |
Clinical Genetics, |
RCV001711862 | SCV002034469 | likely benign | not provided | no assertion criteria provided | clinical testing | ||
Laboratory of Diagnostic Genome Analysis, |
RCV001711862 | SCV002036895 | likely benign | not provided | no assertion criteria provided | clinical testing |