Total submissions: 2
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000898024 | SCV001042206 | benign | not provided | 2023-11-27 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003970004 | SCV004778144 | benign | NSD2-related condition | 2019-08-28 | 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). |