Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001447820 | SCV001650896 | likely benign | Bardet-Biedl syndrome | 2023-12-04 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003965878 | SCV004783156 | likely benign | BBS2-related condition | 2019-09-04 | 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). |