Total submissions: 5
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001590181 | SCV001825939 | likely benign | not provided | 2020-08-19 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 30297972) |
Invitae | RCV002592489 | SCV003301296 | likely benign | Hypertrophic cardiomyopathy 2; Dilated cardiomyopathy 1D; Cardiomyopathy, familial restrictive, 3 | 2022-11-08 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV003446842 | SCV004173719 | likely benign | Dilated cardiomyopathy 1D | 2023-04-11 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV003446843 | SCV004173721 | likely benign | Cardiomyopathy, familial restrictive, 3 | 2023-04-11 | criteria provided, single submitter | clinical testing | |
Genome- |
RCV003446841 | SCV004173722 | likely benign | Hypertrophic cardiomyopathy 2 | 2023-04-11 | criteria provided, single submitter | clinical testing |