Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002104901 | SCV002389685 | benign | Autosomal recessive nonsyndromic hearing loss 66; Isolated neonatal sclerosing cholangitis | 2023-08-04 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002486866 | SCV002800519 | likely benign | Autosomal recessive nonsyndromic hearing loss 66; Nephronophthisis 19; Isolated neonatal sclerosing cholangitis | 2021-12-23 | criteria provided, single submitter | clinical testing |