ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.276A>T (p.Pro92=)

dbSNP: rs1800932
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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 RCV001177263 SCV001341439 likely benign Hereditary cancer-predisposing syndrome 2019-12-09 criteria provided, single submitter clinical testing
GeneDx RCV001540753 SCV001758672 likely benign not provided 2018-11-07 criteria provided, single submitter clinical testing
Invitae RCV002068185 SCV002351668 likely benign Hereditary nonpolyposis colorectal neoplasms 2023-10-30 criteria provided, single submitter clinical testing

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