ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.2782A>G (p.Thr928Ala) (rs1057519255)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Knight Diagnostic Laboratories,Oregon Health and Sciences University RCV000415629 SCV000493757 uncertain significance Lynch syndrome I 2016-03-30 criteria provided, single submitter clinical testing
Ambry Genetics RCV000562226 SCV000662422 uncertain significance Hereditary cancer-predisposing syndrome 2018-04-06 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient or conflicting evidence
Color RCV000562226 SCV000690291 uncertain significance Hereditary cancer-predisposing syndrome 2018-08-28 criteria provided, single submitter clinical testing

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