Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Molecular Diagnosis Center for Deafness | RCV000770836 | SCV001984926 | pathogenic | Autosomal recessive nonsyndromic hearing loss 3 | criteria provided, single submitter | clinical testing | ||
Laboratory of Molecular Medicine, |
RCV000770836 | SCV004171060 | pathogenic | Autosomal recessive nonsyndromic hearing loss 3 | criteria provided, single submitter | clinical testing | ||
Genetic Testing Center for Deafness, |
RCV000770836 | SCV000902337 | likely pathogenic | Autosomal recessive nonsyndromic hearing loss 3 | 2019-02-26 | no assertion criteria provided | case-control |