ClinVar Miner

Submissions for variant NM_000038.6(APC):c.*1556C>G (rs448475)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000358142 SCV000452087 benign APC-Associated Polyposis Disorders 2016-06-14 criteria provided, single submitter clinical testing
Systems Biology Platform Zhejiang California International NanoSystems Institute RCV000074258 SCV000105851 cancer Familial colorectal cancer no assertion criteria provided not provided Converted during submission to other.

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