Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002943690 | SCV003277496 | likely benign | Gingival disorder | 2022-09-09 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003898635 | SCV004711633 | likely benign | FPR1-related disorder | 2021-02-15 | 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). |