Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ambry Genetics | RCV000252440 | SCV000318788 | uncertain significance | Cardiovascular phenotype | 2013-07-12 | criteria provided, single submitter | clinical testing | There is insufficient or conflicting evidence for classification of this alteration. |
Eurofins Ntd Llc |
RCV000729226 | SCV000856869 | uncertain significance | not provided | 2017-09-14 | criteria provided, single submitter | clinical testing | |
Fulgent Genetics, |
RCV002479979 | SCV002790043 | 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 | 2021-10-18 | criteria provided, single submitter | clinical testing | |
Revvity Omics, |
RCV000729226 | SCV003824862 | uncertain significance | not provided | 2019-03-06 | criteria provided, single submitter | clinical testing |