Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000976534 | SCV001124438 | benign | not provided | 2023-10-05 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003943257 | SCV004758284 | likely benign | CDK5RAP2-related disorder | 2021-09-15 | 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). |