Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001500756 | SCV001705554 | likely benign | EGFR-related lung cancer | 2024-01-21 | criteria provided, single submitter | clinical testing | |
Sema4, |
RCV002258293 | SCV002537338 | likely benign | Hereditary cancer-predisposing syndrome | 2021-06-14 | criteria provided, single submitter | curation | |
Prevention |
RCV003956106 | SCV004776339 | likely benign | EGFR-related disorder | 2023-05-30 | criteria provided, single submitter | 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). |