ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.147C>T (p.Ala49=) (rs768803986)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000163365 SCV000213902 likely benign Hereditary cancer-predisposing syndrome 2016-04-28 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Invitae RCV000229806 SCV000283717 likely benign Hereditary nonpolyposis colon cancer 2017-12-01 criteria provided, single submitter clinical testing
Color RCV000163365 SCV000685196 likely benign Hereditary cancer-predisposing syndrome 2016-02-24 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000679215 SCV000805845 likely benign not provided 2017-03-09 criteria provided, single submitter clinical testing

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