Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV003428668 | SCV004157355 | uncertain significance | not provided | 2023-09-01 | criteria provided, single submitter | clinical testing | PDGFRB: PM2, BP4 |
Prevention |
RCV003901070 | SCV004716318 | likely benign | PDGFRB-related disorder | 2023-10-12 | 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). |