ClinVar Miner

Submissions for variant NM_000179.3(MSH6):c.789G>A (p.Val263=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003061943 SCV003346008 likely benign Hereditary nonpolyposis colorectal neoplasms 2022-07-11 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV003477039 SCV004222056 likely benign not provided 2023-05-19 criteria provided, single submitter clinical testing

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