Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000879651 | SCV001022697 | likely benign | not provided | 2024-01-17 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003895403 | SCV004710887 | likely benign | TPP1-related condition | 2023-11-27 | 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). |