Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000665295 | SCV000789389 | uncertain significance | Usher syndrome type 1C; Autosomal recessive nonsyndromic hearing loss 18A | 2017-02-01 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002060812 | SCV002447576 | likely benign | not provided | 2022-03-12 | criteria provided, single submitter | clinical testing |