ClinVar Miner

Submissions for variant NM_000038.6(APC):c.190G>T (p.Gly64Ter) (rs79323615)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000499452 SCV000591016 pathogenic Familial adenomatous polyposis 2015-10-26 criteria provided, single submitter clinical testing
Systems Biology Platform Zhejiang California International NanoSystems Institute RCV000073864 SCV000105457 cancer Familial colorectal cancer no assertion criteria provided not provided Converted during submission to other.

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