Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000922385 | SCV001067813 | likely benign | not provided | 2022-11-01 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003895612 | SCV004711577 | likely benign | FBXL4-related condition | 2021-10-16 | 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). |