Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV003095363 | SCV003484031 | likely benign | not provided | 2023-09-25 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003936555 | SCV004759905 | likely benign | ATR-related disorder | 2019-11-04 | 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). |