Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Revvity Omics, |
RCV003134712 | SCV003816537 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 9 | 2019-02-07 | criteria provided, single submitter | clinical testing | |
Invitae | RCV003778739 | SCV004641419 | likely benign | not provided | 2023-11-17 | criteria provided, single submitter | clinical testing |