Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000863685 | SCV001004388 | benign | Imerslund-Grasbeck syndrome | 2024-01-18 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001772157 | SCV002004199 | likely benign | not provided | 2020-04-06 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003928357 | SCV004745986 | benign | CUBN-related condition | 2019-05-22 | 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). |