ClinVar Miner

Submissions for variant NC_000005.10:g.80654344_80654345insTGGCGCGTCCCGCCCAGGT

dbSNP: rs70991108
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001594851 SCV001828794 benign not provided 2019-04-20 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 29147684)
Labcorp Genetics (formerly Invitae), Labcorp RCV001594851 SCV002401897 benign not provided 2021-02-18 criteria provided, single submitter clinical testing
Department of Pharmacy and Biotechnology, University of Bologna RCV000144918 SCV000187674 uncertain significance Gastrointestinal stromal tumor no assertion criteria provided case-control

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