ClinVar Miner

Submissions for variant NM_005359.5(SMAD4):c.1571_1574delGGATins19 (p.?)

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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 RCV000165521 SCV000216253 uncertain significance Hereditary cancer-predisposing syndrome 2014-08-12 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Detected in individual satisfying established diagnostic critera for classic disease without a clear mutation,Insufficient or conflicting evidence

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