ClinVar Miner

Submissions for variant NM_004484.4(GPC3):c.1033-4250del

dbSNP: rs372010975
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001655806 SCV001864500 benign not provided 2019-08-06 criteria provided, single submitter clinical testing
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV001655806 SCV002010676 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV001529233 SCV001742339 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001529233 SCV001967367 benign not specified no assertion criteria provided clinical testing

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