Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Baylor Genetics | RCV000223938 | SCV004041016 | likely pathogenic | Autosomal dominant nonsyndromic hearing loss 66 | 2023-01-07 | criteria provided, single submitter | clinical testing | |
OMIM | RCV000223938 | SCV000280566 | pathogenic | Autosomal dominant nonsyndromic hearing loss 66 | 2019-07-30 | no assertion criteria provided | literature only |