Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV001253053 | SCV001428572 | likely pathogenic | Adult-onset foveomacular vitelliform dystrophy | 2018-01-18 | criteria provided, single submitter | clinical testing |