Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Blueprint Genetics | RCV001074143 | SCV001239712 | likely pathogenic | Retinal dystrophy | 2019-01-24 | criteria provided, single submitter | clinical testing | |
Department of Clinical Genetics, |
RCV000787765 | SCV000926770 | likely pathogenic | Stargardt disease | 2018-04-01 | no assertion criteria provided | research |