Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Gene |
RCV000485334 | SCV000571540 | benign | not specified | 2016-11-29 | criteria provided, single submitter | clinical testing | This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease. |
Invitae | RCV000528935 | SCV000652815 | benign | Methylmalonic acidemia with homocystinuria, type cblJ | 2024-01-18 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003902727 | SCV004722147 | benign | ABCD4-related condition | 2019-04-26 | criteria provided, single submitter | clinical testing | This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications). |