Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
NIHR Bioresource Rare Diseases, |
RCV000505086 | SCV000599100 | likely pathogenic | Retinitis pigmentosa | 2015-01-01 | no assertion criteria provided | research | |
Laboratory of Genetics in Ophthalmology, |
RCV001261187 | SCV001438587 | pathogenic | Leber congenital amaurosis 6 | no assertion criteria provided | research |