Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001596766 | SCV001832119 | benign | not provided | 2015-03-03 | criteria provided, single submitter | clinical testing | This variant is associated with the following publications: (PMID: 25351510) |
Clinical Genetics, |
RCV001596766 | SCV001918574 | likely benign | not provided | no assertion criteria provided | clinical testing | ||
Diagnostic Laboratory, |
RCV001596766 | SCV001963383 | likely benign | not provided | no assertion criteria provided | clinical testing |