Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000227056 | SCV000288333 | likely benign | Neuroblastoma, susceptibility to, 3 | 2024-01-27 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003897549 | SCV004715554 | likely benign | ALK-related condition | 2022-07-21 | 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). |