Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000978168 | SCV001126094 | likely benign | Immunodeficiency, common variable, 7 | 2024-01-03 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003962939 | SCV004785106 | likely benign | CR2-related condition | 2019-08-26 | criteria provided, single submitter | clinical testing | This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |