Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000653823 | SCV000775713 | likely benign | Drash syndrome; Frasier syndrome; Wilms tumor 1; 11p partial monosomy syndrome | 2023-11-13 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002493054 | SCV002800390 | likely benign | Aniridia 1; Drash syndrome; Frasier syndrome; Meacham syndrome; Mesothelioma, malignant; Nephrotic syndrome, type 4; Wilms tumor 1; 11p partial monosomy syndrome | 2021-10-26 | criteria provided, single submitter | clinical testing | |
All of Us Research Program, |
RCV004004109 | SCV004828261 | likely benign | Wilms tumor 1 | 2023-05-30 | criteria provided, single submitter | clinical testing |