Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000534951 | SCV000625719 | benign | Common variable immunodeficiency | 2024-01-29 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003905323 | SCV004726720 | benign | TNFSF12-related condition | 2019-06-17 | criteria provided, single submitter | clinical testing | This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |