Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV000488318 | SCV000574996 | uncertain significance | not provided | 2016-10-01 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV000765201 | SCV000896436 | uncertain significance | Prader-Willi syndrome; Schaaf-Yang syndrome | 2018-10-31 | criteria provided, single submitter | clinical testing |