ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.2805_2806insTT (p.Asp936fs) (rs876659189)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000218854 SCV000275354 pathogenic Hereditary cancer-predisposing syndrome 2015-04-17 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Alterations resulting in premature truncation (e.g.reading frame shift, nonsense)

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