Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002079687 | SCV002429990 | benign | not provided | 2024-01-02 | criteria provided, single submitter | clinical testing | |
Ce |
RCV002079687 | SCV004183864 | likely benign | not provided | 2023-11-01 | criteria provided, single submitter | clinical testing | FN1: BP4, BS1 |
Prevention |
RCV003913778 | SCV004746923 | benign | FN1-related disorder | 2019-09-19 | no assertion criteria provided | clinical testing | This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |