Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000668427 | SCV000793026 | uncertain significance | Usher syndrome type 1C; Autosomal recessive nonsyndromic hearing loss 18A | 2017-07-26 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002507161 | SCV002814133 | uncertain significance | Usher syndrome type 1C; Autosomal recessive nonsyndromic hearing loss 18A; Usher syndrome type 1 | 2021-12-17 | criteria provided, single submitter | clinical testing |