Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000896161 | SCV001040241 | benign | not provided | 2024-01-05 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003910672 | SCV004722988 | likely benign | PLXNA2-related disorder | 2021-07-19 | 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). |