Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000669113 | SCV000793826 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 1A | 2017-11-14 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001855515 | SCV002180444 | uncertain significance | not provided | 2021-10-14 | criteria provided, single submitter | clinical testing |