Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV000630998 | SCV000751978 | likely benign | Fanconi anemia | 2024-01-08 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003892413 | SCV004710942 | likely benign | FANCD2-related disorder | 2021-10-25 | 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). |