ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.2538A>G (p.Glu846=)

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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 RCV003584506 SCV004357655 likely benign Hereditary cancer-predisposing syndrome 2023-04-26 criteria provided, single submitter clinical testing
Invitae RCV003759895 SCV004452386 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-04-07 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004011498 SCV004824832 likely benign Lynch syndrome 2023-05-04 criteria provided, single submitter clinical testing

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