ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.3664T>G (p.Phe1222Val) (rs775265464)

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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 RCV000491642 SCV000580126 uncertain significance Hereditary cancer-predisposing syndrome 2014-05-29 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient or conflicting evidence
Color RCV000491642 SCV000908428 uncertain significance Hereditary cancer-predisposing syndrome 2018-10-05 criteria provided, single submitter clinical testing

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