Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002123015 | SCV002405517 | benign | Brachyolmia-amelogenesis imperfecta syndrome | 2024-01-08 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003970913 | SCV004779751 | likely benign | LTBP3-related disorder | 2020-11-10 | 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). |