Total submissions: 1
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Centre for Mendelian Genomics, |
RCV000626763 | SCV000747466 | uncertain significance | Retinal detachment; Visual impairment; Rod-cone dystrophy; Central scotoma; Blurred vision | 2017-01-01 | criteria provided, single submitter | clinical testing |