Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV001513179 | SCV001720744 | benign | not provided | 2024-01-29 | criteria provided, single submitter | clinical testing | |
Gene |
RCV001513179 | SCV001774037 | likely benign | not provided | 2020-11-22 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003921097 | SCV004728858 | benign | FN1-related disorder | 2019-06-21 | 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). |