ClinVar Miner

Submissions for variant NM_206933.3(USH2A):c.13297G>T (p.Val4433Leu) (rs111033381)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000041738 SCV000231900 benign not specified 2014-07-22 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000041738 SCV000065434 benign not specified 2010-06-17 criteria provided, single submitter clinical testing
NEI Ophthalmic Genomics Laboratory,National Institutes of Health RCV000087006 SCV000119259 not provided not provided no assertion provided not provided

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