Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000664966 | SCV000789012 | uncertain significance | Usher syndrome type 1C; Autosomal recessive nonsyndromic hearing loss 18A | 2016-12-27 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001397163 | SCV001598908 | likely benign | not provided | 2021-04-04 | criteria provided, single submitter | clinical testing |