Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Mendelics | RCV002247481 | SCV002516099 | uncertain significance | not specified | 2022-05-04 | criteria provided, single submitter | clinical testing | |
OMIM | RCV000083259 | SCV000115338 | pathogenic | Autosomal dominant nonsyndromic hearing loss 56 | 2013-07-30 | no assertion criteria provided | literature only |