ClinVar Miner

Submissions for variant NM_001933.5(DLST):c.147-17G>C

dbSNP: rs201278080
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute for Clinical Genetics, University Hospital TU Dresden, University Hospital TU Dresden RCV003238531 SCV002010503 uncertain significance not provided 2021-11-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003238531 SCV004366227 likely benign not provided 2024-01-09 criteria provided, single submitter clinical testing

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