Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002077876 | SCV002324179 | likely benign | RASopathy | 2023-12-16 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV004538769 | SCV004713246 | likely benign | CBL-related disorder | 2021-11-04 | no assertion criteria provided | 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). |