Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003613006 | SCV004560485 | likely benign | Mowat-Wilson syndrome | 2023-08-10 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003893380 | SCV004716725 | likely benign | ZEB2-related disorder | 2021-11-11 | 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). |