Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000462788 | SCV000542924 | uncertain significance | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2016-12-13 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001550296 | SCV001770601 | likely benign | not provided | 2020-02-06 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 32880476) |