Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000977910 | SCV001125832 | benign | Rett syndrome, congenital variant | 2023-11-18 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003953363 | SCV004775888 | likely benign | FOXG1-related disorder | 2020-02-10 | no assertion criteria provided | 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). |