Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Ce |
RCV000416233 | SCV000493395 | uncertain significance | not provided | 2016-08-01 | criteria provided, single submitter | clinical testing | |
Invitae | RCV000416233 | SCV001033824 | likely benign | not provided | 2023-12-27 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003897835 | SCV004722713 | likely benign | GRM6-related condition | 2019-09-05 | 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). |