ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.816A>G (p.Glu272=)

dbSNP: rs863224631
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000542687 SCV000625005 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-11-24 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000776691 SCV000912319 likely benign Hereditary cancer-predisposing syndrome 2017-10-27 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004003704 SCV004837063 likely benign Lynch syndrome 2023-08-15 criteria provided, single submitter clinical testing

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