Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Institute of Human Genetics, |
RCV000408588 | SCV000281811 | uncertain significance | Severe early-childhood-onset retinal dystrophy | 2016-01-01 | criteria provided, single submitter | clinical testing | |
Ce |
RCV000513081 | SCV000608484 | uncertain significance | not provided | 2017-02-01 | criteria provided, single submitter | clinical testing |