ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.2949G>C (p.Glu983Asp) (rs780485157)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000499422 SCV000592619 uncertain significance Lynch syndrome 2013-11-08 criteria provided, single submitter clinical testing
Ambry Genetics RCV000573654 SCV000664985 uncertain significance Hereditary cancer-predisposing syndrome 2017-08-01 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence,In silico models in agreement (benign)

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