Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Labcorp Genetics |
RCV003699878 | SCV004464161 | benign | not provided | 2022-11-18 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV004539070 | SCV004719998 | likely benign | PPA2-related disorder | 2019-08-09 | criteria provided, single submitter | 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). |