ClinVar Miner

Submissions for variant NM_032119.4(ADGRV1):c.9927T>G (p.Pro3309=) (rs16869042)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000039665 SCV000063354 benign not specified 2010-03-23 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000039665 SCV000230753 benign not specified 2015-07-07 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000039665 SCV000314881 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000755457 SCV000602438 benign not provided 2017-05-02 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV000039665 SCV000193302 likely benign not specified no assertion criteria provided clinical testing

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