Total submissions: 3
Submitter | RCV | SCV | Clinical significance | Condition | Last evaluated | Review status | Method | Comment |
---|---|---|---|---|---|---|---|---|
Eurofins Ntd Llc |
RCV000277239 | SCV000335802 | benign | not specified | 2015-10-08 | criteria provided, single submitter | clinical testing | |
Labcorp Genetics |
RCV000968221 | SCV001115660 | benign | not provided | 2024-01-31 | criteria provided, single submitter | clinical testing | |
Prevention |
RCV003955452 | SCV004773165 | likely benign | TCIRG1-related disorder | 2024-01-16 | 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). |