Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000975535 | SCV001123421 | likely benign | not provided | 2024-01-11 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002503108 | SCV002804651 | likely benign | Autosomal dominant nonsyndromic hearing loss 11; Autosomal recessive nonsyndromic hearing loss 2; Usher syndrome type 1 | 2022-05-13 | criteria provided, single submitter | clinical testing |