Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000528292 | SCV000625721 | benign | Common variable immunodeficiency | 2024-01-31 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003905324 | SCV004719368 | likely benign | TNFSF12-related condition | 2019-08-09 | 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). |