Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000903983 | SCV001048476 | benign | not provided | 2018-05-03 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003968287 | SCV004781796 | likely benign | CAVIN1-related disorder | 2022-01-03 | 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). |