Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Molecular Diagnosis Center for Deafness | RCV001822951 | SCV001984901 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 3 | criteria provided, single submitter | clinical testing | ||
Wang |
RCV001822951 | SCV001762500 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 3 | 2021-07-01 | no assertion criteria provided | clinical testing |