Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Center for Pediatric Genomic Medicine, |
RCV000514304 | SCV000610359 | likely benign | not provided | 2017-07-24 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000514304 | SCV001037709 | benign | not provided | 2019-12-31 | criteria provided, single submitter | clinical testing | |
Athena Diagnostics Inc | RCV000514304 | SCV001146209 | benign | not provided | 2018-11-14 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000514304 | SCV001865808 | benign | not provided | 2020-01-06 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV002270612 | SCV002554472 | benign | Autosomal dominant nonsyndromic hearing loss 56 | 2022-03-15 | criteria provided, single submitter | clinical testing |