Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003004979 | SCV003300257 | benign | not provided | 2023-11-24 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003963556 | SCV004779401 | likely benign | PTPRO-related disorder | 2020-01-15 | 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). |