Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002092007 | SCV002325380 | likely benign | Brachyolmia-amelogenesis imperfecta syndrome | 2023-09-26 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003958481 | SCV004775521 | likely benign | LTBP3-related disorder | 2024-01-08 | 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). |