ClinVar Miner

Submissions for variant NM_000038.6(APC):c.5880G>A (p.Pro1960=) (rs465899)

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Total submissions: 11
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000035080 SCV000109829 benign not specified 2016-03-16 criteria provided, single submitter clinical testing
Ambry Genetics RCV000162375 SCV000212685 benign Hereditary cancer-predisposing syndrome 2014-10-29 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000035080 SCV000301602 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000270059 SCV000452031 benign APC-Associated Polyposis Disorders 2016-06-14 criteria provided, single submitter clinical testing
Department of Pathology and Laboratory Medicine,Sinai Health System RCV000035080 SCV000591193 benign not specified 2012-04-20 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000755460 SCV000602519 benign not provided 2017-05-08 criteria provided, single submitter clinical testing
Invitae RCV000755460 SCV000647613 benign not provided 2019-03-06 criteria provided, single submitter clinical testing
Color RCV000162375 SCV000681767 benign Hereditary cancer-predisposing syndrome 2016-03-18 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000035080 SCV000058720 benign not specified 2008-03-01 no assertion criteria provided clinical testing
Systems Biology Platform Zhejiang California International NanoSystems Institute RCV000074242 SCV000105835 cancer Familial colorectal cancer no assertion criteria provided not provided Converted during submission to other.
Mayo Clinic Genetic Testing Laboratories,Mayo Clinic RCV000035080 SCV000257018 benign not specified no assertion criteria provided clinical testing

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