Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002174825 | SCV002347439 | likely benign | Autosomal recessive nonsyndromic hearing loss 66; Isolated neonatal sclerosing cholangitis | 2024-10-15 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002494055 | SCV002799956 | likely benign | Autosomal recessive nonsyndromic hearing loss 66; Nephronophthisis 19; Isolated neonatal sclerosing cholangitis | 2021-09-28 | criteria provided, single submitter | clinical testing |