ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.4002-28_4002-26dup

gnomAD frequency: 0.00238  dbSNP: rs200989473
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001189177 SCV001356412 benign Hereditary cancer-predisposing syndrome 2018-11-06 criteria provided, single submitter clinical testing
GeneDx RCV001673031 SCV001887795 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV003493813 SCV004243107 likely benign not specified 2024-02-06 criteria provided, single submitter clinical testing

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