ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.3173-10C>A

dbSNP: rs587780559
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001703861 SCV000526070 likely benign not provided 2019-06-26 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 26976419)
Invitae RCV000526975 SCV000624826 likely benign Hereditary nonpolyposis colorectal neoplasms 2024-01-03 criteria provided, single submitter clinical testing
Color Diagnostics, LLC DBA Color Health RCV000580406 SCV000685363 likely benign Hereditary cancer-predisposing syndrome 2015-06-01 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV004000420 SCV004834562 likely benign Lynch syndrome 2024-02-05 criteria provided, single submitter clinical testing

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