Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000536908 | SCV000642572 | uncertain significance | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2017-07-20 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001722486 | SCV000730445 | likely benign | not provided | 2019-10-01 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 30847666) |
Revvity Omics, |
RCV001722486 | SCV003818364 | uncertain significance | not provided | 2021-06-06 | criteria provided, single submitter | clinical testing |