Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000921189 | SCV001066586 | likely benign | Immunodeficiency 18 | 2024-01-29 | criteria provided, single submitter | clinical testing | |
Baylor Genetics | RCV000921189 | SCV001527443 | uncertain significance | Immunodeficiency 18 | 2018-08-24 | criteria provided, single submitter | clinical testing | This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868]. |