Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
CHEO Genetics Diagnostic Laboratory, |
RCV000769060 | SCV000900433 | uncertain significance | Cardiomyopathy | 2016-03-22 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002485981 | SCV002780817 | uncertain significance | 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 | 2021-10-13 | criteria provided, single submitter | clinical testing |