ClinVar Miner

Submissions for variant NM_005359.5(SMAD4):c.*2707_*2711delCTTTA (rs769541605)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000346667 SCV000409213 uncertain significance Juvenile Polyposis 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000390407 SCV000409214 uncertain significance Hereditary hemorrhagic telangiectasia type 1 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000302424 SCV000409215 uncertain significance Myhre syndrome 2016-06-14 criteria provided, single submitter clinical testing

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