Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002928760 | SCV003275157 | benign | not provided | 2023-12-20 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV004548428 | SCV004766964 | likely benign | FAT1-related disorder | 2020-01-22 | 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). |