Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome- |
RCV001578921 | SCV001806280 | uncertain significance | Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3 | 2021-07-22 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001578922 | SCV001806281 | uncertain significance | Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3 | 2021-07-22 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001578923 | SCV001806282 | uncertain significance | Autosomal recessive limb-girdle muscular dystrophy type 2O | 2021-07-22 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001578924 | SCV001806283 | uncertain significance | Retinitis pigmentosa 76 | 2021-07-22 | criteria provided, single submitter | clinical testing |