Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome- |
RCV001579109 | SCV001806512 | uncertain significance | Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3 | 2021-07-22 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001579110 | SCV001806513 | uncertain significance | Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3 | 2021-07-22 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001579111 | SCV001806514 | uncertain significance | Autosomal recessive limb-girdle muscular dystrophy type 2O | 2021-07-22 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001579112 | SCV001806515 | uncertain significance | Retinitis pigmentosa 76 | 2021-07-22 | criteria provided, single submitter | clinical testing |