Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001402389 | SCV001604236 | likely benign | Pierson syndrome; LAMB2-related infantile-onset nephrotic syndrome | 2023-01-01 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV001402389 | SCV002813125 | likely benign | Pierson syndrome; LAMB2-related infantile-onset nephrotic syndrome | 2022-04-16 | criteria provided, single submitter | clinical testing |