Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000868124 | SCV001009421 | likely benign | Wilms tumor 1 | 2023-11-24 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003975415 | SCV004795377 | likely benign | GPC3-related disorder | 2023-10-24 | 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). |