ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.2805_2806del (p.Asp936fs) (rs863225403)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000491348 SCV000580174 pathogenic Hereditary cancer-predisposing syndrome 2016-06-25 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)
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000202273 SCV000257229 likely pathogenic not provided no assertion criteria provided research

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