Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000969906 | SCV001117452 | likely benign | Autosomal recessive limb-girdle muscular dystrophy type 2O; Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3 | 2024-01-05 | criteria provided, single submitter | clinical testing | |
Genetic Services Laboratory, |
RCV001819098 | SCV002067792 | likely benign | not specified | 2019-01-18 | criteria provided, single submitter | clinical testing |