Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002630558 | SCV002958893 | likely benign | Fanconi anemia | 2022-04-24 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV004534144 | SCV004713689 | likely benign | FANCM-related disorder | 2022-02-03 | 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). |