Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003529242 | SCV004282052 | likely benign | Noonan syndrome | 2023-07-28 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003901169 | SCV004709030 | likely benign | RRAS-related disorder | 2020-11-13 | 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). |