Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome- |
RCV001549071 | SCV001769150 | benign | Autosomal recessive nonsyndromic hearing loss 44 | 2021-07-14 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001676053 | SCV001895679 | benign | not provided | 2018-11-10 | criteria provided, single submitter | clinical testing |