ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.457+32TG[12]

dbSNP: rs397839804
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000409204 SCV000488155 uncertain significance Lynch syndrome 5 2016-02-19 criteria provided, single submitter clinical testing
Mendelics RCV000409204 SCV001135786 likely benign Lynch syndrome 5 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001536952 SCV001753770 benign not provided 2019-08-30 criteria provided, single submitter clinical testing
Center for Genomic Medicine, Rigshospitalet, Copenhagen University Hospital RCV002267835 SCV002552277 likely benign not specified 2023-08-15 criteria provided, single submitter clinical testing

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