ClinVar Miner

Submissions for variant NM_000179.2(MSH6):c.2329T>A (p.Trp777Arg) (rs267608067)

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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 RCV000130193 SCV000185030 uncertain significance Hereditary cancer-predisposing syndrome 2016-10-11 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence
Color RCV000130193 SCV000908397 uncertain significance Hereditary cancer-predisposing syndrome 2018-07-17 criteria provided, single submitter clinical testing

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