Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Prevention |
RCV000250172 | SCV000305601 | benign | not specified | criteria provided, single submitter | clinical testing | ||
Gene |
RCV000830449 | SCV000972184 | benign | not provided | 2018-06-16 | 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. |
Genome- |
RCV001838567 | SCV002098600 | benign | Dilated cardiomyopathy 1D | 2021-09-10 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001838568 | SCV002098601 | benign | Cardiomyopathy, familial restrictive, 3 | 2021-09-10 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV001838566 | SCV002098602 | benign | Hypertrophic cardiomyopathy 2 | 2021-09-10 | criteria provided, single submitter | clinical testing |