Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV003415058 | SCV004127398 | likely benign | not provided | 2023-10-01 | criteria provided, single submitter | clinical testing | FMN2: BP4, BP7 |
Prevention |
RCV003954112 | SCV004770142 | likely benign | FMN2-related disorder | 2020-08-17 | 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). |