ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.513A>G (p.Glu171=) (rs786201116)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000162695 SCV000213150 likely benign Hereditary cancer-predisposing syndrome 2015-12-20 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Synonymous alterations with insufficient evidence to classify as benign
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000502233 SCV000592569 likely benign not specified 2016-08-05 criteria provided, single submitter clinical testing
Color RCV000162695 SCV000690447 likely benign Hereditary cancer-predisposing syndrome 2017-08-31 criteria provided, single submitter clinical testing
Integrated Genetics/Laboratory Corporation of America RCV000502233 SCV000919771 likely benign not specified 2019-08-29 criteria provided, single submitter clinical testing
Invitae RCV000980082 SCV001128030 likely benign not provided 2018-12-07 criteria provided, single submitter clinical testing

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