Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV002212831 | SCV002368074 | likely benign | Neurofibromatosis, type 1 | 2021-08-10 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV004553680 | SCV004800253 | likely benign | NF1-related disorder | 2023-12-15 | 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). |