Total submissions: 7
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Illumina Laboratory Services, |
RCV000305886 | SCV000372380 | uncertain significance | Left ventricular noncompaction cardiomyopathy | 2016-06-14 | criteria provided, single submitter | clinical testing | |
Illumina Laboratory Services, |
RCV000360595 | SCV000372381 | uncertain significance | Hypertrophic cardiomyopathy | 2016-06-14 | criteria provided, single submitter | clinical testing | |
Illumina Laboratory Services, |
RCV000396667 | SCV000372382 | uncertain significance | Dilated Cardiomyopathy, Dominant | 2016-06-14 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001711908 | SCV000726255 | likely benign | not provided | 2021-05-26 | criteria provided, single submitter | clinical testing | Has not been previously published as pathogenic or benign to our knowledge; This variant is associated with the following publications: (PMID: 32841044) |
Color Diagnostics, |
RCV001176816 | SCV001340875 | likely benign | Cardiomyopathy | 2019-03-07 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000360595 | SCV002400994 | likely benign | Hypertrophic cardiomyopathy | 2023-12-12 | criteria provided, single submitter | clinical testing | |
CHEO Genetics Diagnostic Laboratory, |
RCV001176816 | SCV004239397 | uncertain significance | Cardiomyopathy | 2022-07-18 | criteria provided, single submitter | clinical testing |