Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV000513415 | SCV000608877 | likely pathogenic | not provided | 2017-07-01 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002496975 | SCV002816055 | likely pathogenic | Intellectual developmental disorder, autosomal recessive 68 | 2021-07-23 | criteria provided, single submitter | clinical testing |