ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.2701C>G (p.Arg901Gly) (rs772514245)

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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 RCV000566629 SCV000670070 uncertain significance Hereditary cancer-predisposing syndrome 2017-04-26 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Confirmed de novo alteration in the setting of a new disease (appropriate phenotype) in the family

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