Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000547861 | SCV000642849 | uncertain significance | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2017-06-28 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002491034 | SCV002797640 | 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 | 2021-07-28 | criteria provided, single submitter | clinical testing | |
Revvity Omics, |
RCV003139785 | SCV003821151 | uncertain significance | not provided | 2019-08-22 | criteria provided, single submitter | clinical testing | |
CHEO Genetics Diagnostic Laboratory, |
RCV003486864 | SCV004239863 | likely benign | Cardiomyopathy | 2023-05-16 | criteria provided, single submitter | clinical testing |