Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Counsyl | RCV000668978 | SCV000793665 | uncertain significance | Pendred syndrome | 2017-08-22 | criteria provided, single submitter | clinical testing | |
Baylor Genetics | RCV003472108 | SCV004201891 | likely pathogenic | Autosomal recessive nonsyndromic hearing loss 4 | 2023-08-13 | criteria provided, single submitter | clinical testing |