Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV001707674 | SCV000718502 | likely benign | not provided | 2020-02-20 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003950260 | SCV004761895 | likely benign | TRDN-related condition | 2023-12-16 | 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). |