Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000880776 | SCV001023898 | benign | not provided | 2024-01-18 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003948305 | SCV004759566 | likely benign | TUBGCP6-related disorder | 2020-02-19 | 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). |
Ce |
RCV000880776 | SCV004810908 | likely benign | not provided | 2024-03-01 | criteria provided, single submitter | clinical testing | TUBGCP6: BP4, BP7, BS2 |