ClinVar Miner

Submissions for variant NM_153676.4(USH1C):c.105-16C>T (rs2041027)

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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 RCV000041247 SCV000064938 benign not specified 2009-06-24 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000041247 SCV000316305 benign not specified criteria provided, single submitter clinical testing
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000041247 SCV000854884 benign not specified 2017-07-21 criteria provided, single submitter clinical testing
Invitae RCV001513061 SCV001720594 benign not provided 2020-11-27 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000041247 SCV001741964 benign not specified no assertion criteria provided clinical testing

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