Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002904946 | SCV003261219 | likely benign | Noonan syndrome | 2023-06-28 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV004754903 | SCV005362199 | likely benign | RRAS-related disorder | 2024-09-11 | 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). |