ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.2004C>T (p.Ser668=)

dbSNP: rs766113887
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001184177 SCV001350095 likely benign Hereditary cancer-predisposing syndrome 2019-12-04 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001194396 SCV001363904 likely benign not specified 2019-11-20 criteria provided, single submitter clinical testing

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