Total submissions: 4
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV001086662 | SCV000294271 | likely benign | Renal cell carcinoma | 2024-02-01 | criteria provided, single submitter | clinical testing | |
Gene |
RCV000828224 | SCV000969908 | likely benign | not provided | 2020-12-09 | criteria provided, single submitter | clinical testing | |
Sema4, |
RCV002255343 | SCV002532128 | likely benign | Hereditary cancer-predisposing syndrome | 2022-02-09 | criteria provided, single submitter | curation | |
Prevention |
RCV004745306 | SCV005347529 | likely benign | MET-related disorder | 2024-03-09 | 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). |