ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3173-14CT[2]

dbSNP: rs746607182
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001696861 SCV000569364 likely benign not provided 2019-03-11 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000579813 SCV000685362 likely benign Hereditary cancer-predisposing syndrome 2016-07-01 criteria provided, single submitter clinical testing
Invitae RCV002056774 SCV002359366 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-09-25 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004003327 SCV004832507 likely benign Lynch syndrome 2023-10-23 criteria provided, single submitter clinical testing

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