Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000528154 | SCV000622179 | likely benign | Alzheimer disease | 2023-12-11 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003942720 | SCV004772282 | likely benign | APP-related condition | 2019-12-18 | 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). |