Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001719960 | SCV000513441 | likely benign | not provided | 2019-01-03 | criteria provided, single submitter | clinical testing | |
Ambry Genetics | RCV000620003 | SCV000737316 | uncertain significance | Cardiovascular phenotype | 2017-10-10 | criteria provided, single submitter | clinical testing | There is insufficient or conflicting evidence for classification of this alteration. |
CHEO Genetics Diagnostic Laboratory, |
RCV000769184 | SCV000900560 | uncertain significance | Cardiomyopathy | 2016-05-05 | criteria provided, single submitter | clinical testing | |
Laboratory for Molecular Medicine, |
RCV000154731 | SCV000204411 | not provided | not specified | 2013-04-26 | no assertion provided | clinical testing |