Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Centre for Mendelian Genomics, |
RCV000414889 | SCV000492953 | uncertain significance | Right ventricular cardiomyopathy | 2013-12-13 | criteria provided, single submitter | clinical testing | |
Centre for Mendelian Genomics, |
RCV001198382 | SCV001369294 | uncertain significance | Tibial muscular dystrophy | 2016-01-01 | criteria provided, single submitter | clinical testing | This variant was classified as: Uncertain significance. |