Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001688677 | SCV001915289 | benign | not provided | 2018-06-24 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001788787 | SCV002029338 | benign | Autosomal recessive nonsyndromic hearing loss 9 | 2021-09-05 | criteria provided, single submitter | clinical testing |