Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001465737 | SCV001669729 | likely benign | Bardet-Biedl syndrome | 2023-11-09 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003900606 | SCV004710808 | likely benign | BBS2-related condition | 2021-08-31 | 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). |