Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
CHEO Genetics Diagnostic Laboratory, |
RCV001799186 | SCV002042453 | likely benign | Cardiomyopathy | 2019-07-15 | criteria provided, single submitter | clinical testing | |
Invitae | RCV002074138 | SCV002348205 | likely benign | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2023-06-23 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002489846 | SCV002803199 | likely benign | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure; Early-onset myopathy with fatal cardiomyopathy; Hypertrophic cardiomyopathy 9 | 2021-08-25 | criteria provided, single submitter | clinical testing |