Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000461627 | SCV000555126 | likely benign | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2022-12-06 | criteria provided, single submitter | clinical testing | |
CHEO Genetics Diagnostic Laboratory, |
RCV001171035 | SCV001333704 | likely benign | Cardiomyopathy | 2018-08-21 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001548519 | SCV001768446 | likely benign | not provided | 2019-03-28 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002489094 | SCV002799856 | 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 | 2021-08-20 | criteria provided, single submitter | clinical testing |