Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Fulgent Genetics, |
RCV000186353 | SCV002814135 | likely pathogenic | Primary hyperoxaluria, type I | 2022-02-05 | criteria provided, single submitter | clinical testing | |
Clinical Biochemistry Laboratory, |
RCV000186353 | SCV000239700 | pathogenic | Primary hyperoxaluria, type I | 2014-11-27 | no assertion criteria provided | in vivo |