ClinVar Miner

Submissions for variant NM_206933.3(USH2A):c.5857+17A>C (rs74766738)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000241906 SCV000317208 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001289565 SCV001477522 benign none provided 2019-10-21 criteria provided, single submitter clinical testing
Invitae RCV001519719 SCV001728639 benign not provided 2020-11-17 criteria provided, single submitter clinical testing
GeneDx RCV001519719 SCV001757458 benign not provided 2015-03-03 criteria provided, single submitter clinical testing

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