Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000917428 | SCV001062705 | likely benign | not provided | 2024-01-14 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002502780 | SCV002811189 | likely benign | Usher syndrome type 1C; Autosomal recessive nonsyndromic hearing loss 18A; Usher syndrome type 1 | 2021-07-12 | criteria provided, single submitter | clinical testing | |
Natera, |
RCV001276300 | SCV001462416 | uncertain significance | Usher syndrome type 1C | 2020-04-11 | no assertion criteria provided | clinical testing |