ClinVar Miner

Submissions for variant NM_021978.4(ST14):c.1224-6dup

dbSNP: rs11368852
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001727872 SCV002372389 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001529767 SCV001743816 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001727872 SCV001973661 likely benign not provided no assertion criteria provided clinical testing

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