Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000463818 | SCV000542795 | uncertain significance | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2016-11-26 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002481380 | SCV002780470 | 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 | 2021-12-27 | criteria provided, single submitter | clinical testing | |
Revvity Omics, |
RCV003139627 | SCV003826633 | uncertain significance | not provided | 2020-07-10 | criteria provided, single submitter | clinical testing | |
Ce |
RCV003139627 | SCV004150238 | uncertain significance | not provided | 2023-07-01 | criteria provided, single submitter | clinical testing |