Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome- |
RCV001578955 | SCV001806322 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 4 | 2021-07-22 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001578956 | SCV001806323 | uncertain significance | Pendred syndrome | 2021-07-22 | criteria provided, single submitter | clinical testing |