Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome- |
RCV001563774 | SCV001786800 | uncertain significance | Autosomal recessive nonsyndromic hearing loss 77 | 2021-07-14 | criteria provided, single submitter | clinical testing |