Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Biesecker Lab/Clinical Genomics Section, |
RCV000172321 | SCV000051168 | uncertain significance | not provided | 2013-06-24 | criteria provided, single submitter | research | |
Invitae | RCV000551726 | SCV000643264 | uncertain significance | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2017-06-28 | criteria provided, single submitter | clinical testing | |
Ce |
RCV000172321 | SCV001152895 | uncertain significance | not provided | 2017-05-01 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002478555 | SCV002792560 | 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 | 2021-09-16 | criteria provided, single submitter | clinical testing |