ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.105C>T (p.Ala35=) (rs998365223)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color RCV000772631 SCV000905827 likely benign Hereditary cancer-predisposing syndrome 2015-12-10 criteria provided, single submitter clinical testing
Invitae RCV000630399 SCV000751355 likely benign Hereditary nonpolyposis colon cancer 2017-09-19 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000506243 SCV000601501 uncertain significance not specified 2017-06-15 criteria provided, single submitter clinical testing

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