Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Genome Diagnostics Laboratory, |
RCV002264596 | SCV002543340 | benign | Autoinflammatory syndrome | 2019-05-01 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003926350 | SCV004743499 | benign | CARD14-related disorder | 2019-05-22 | 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). |