Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Fulgent Genetics, |
RCV002505519 | SCV002816189 | 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 | 2021-08-26 | criteria provided, single submitter | clinical testing | |
Revvity Omics, |
RCV000997598 | SCV003819648 | uncertain significance | not provided | 2020-02-12 | criteria provided, single submitter | clinical testing | |
Clinical Genetics, |
RCV000997598 | SCV001921451 | uncertain significance | not provided | no assertion criteria provided | clinical testing | ||
Clinical Genetics DNA and cytogenetics Diagnostics Lab, |
RCV000997598 | SCV001970625 | uncertain significance | not provided | no assertion criteria provided | clinical testing |