Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Blueprint Genetics | RCV001073638 | SCV001239189 | likely pathogenic | Retinal dystrophy | 2019-07-26 | criteria provided, single submitter | clinical testing | |
Baylor Genetics | RCV003470637 | SCV004193531 | pathogenic | Retinitis pigmentosa 25 | 2023-02-20 | criteria provided, single submitter | clinical testing | |
NIHR Bioresource Rare Diseases, |
RCV000504800 | SCV000599153 | likely pathogenic | Retinitis pigmentosa | 2015-01-01 | no assertion criteria provided | research |