Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000698946 | SCV000827637 | likely benign | Congenital hyperammonemia, type I | 2024-02-01 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002485710 | SCV002792811 | uncertain significance | Congenital hyperammonemia, type I; Pulmonary hypertension, neonatal, susceptibility to | 2021-07-11 | criteria provided, single submitter | clinical testing | |
Natera, |
RCV000698946 | SCV002076228 | uncertain significance | Congenital hyperammonemia, type I | 2019-10-28 | no assertion criteria provided | clinical testing |