Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000184129 | SCV000236741 | benign | not specified | 2014-06-23 | criteria provided, single submitter | clinical testing | This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. |
Eurofins Ntd Llc |
RCV000725528 | SCV000337533 | uncertain significance | not provided | 2015-11-12 | criteria provided, single submitter | clinical testing | |
Invitae | RCV001087956 | SCV000555399 | likely benign | Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J | 2024-01-18 | criteria provided, single submitter | clinical testing | |
Athena Diagnostics Inc | RCV000725528 | SCV001146338 | likely benign | not provided | 2018-11-05 | criteria provided, single submitter | clinical testing | |
CHEO Genetics Diagnostic Laboratory, |
RCV001798644 | SCV002042398 | likely benign | Cardiomyopathy | 2020-04-20 | criteria provided, single submitter | clinical testing |