Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Invitae | RCV000910003 | SCV001054844 | benign | not provided | 2023-02-26 | criteria provided, single submitter | clinical testing | |
Genetic Services Laboratory, |
RCV001818823 | SCV002070262 | likely benign | not specified | 2020-06-01 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003968385 | SCV004777432 | likely benign | INSR-related condition | 2020-01-13 | 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). |