Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000964139 | SCV001111326 | likely benign | Familial hemophagocytic lymphohistiocytosis 2 | 2024-01-20 | criteria provided, single submitter | clinical testing | |
Baylor Genetics | RCV001335646 | SCV001528837 | uncertain significance | Aplastic anemia | 2018-04-27 | criteria provided, single submitter | clinical testing | This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868]. |