ClinVar Miner

Submissions for variant NM_153676.4(USH1C):c.1069C>T (p.Arg357Trp) (rs140934960)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000174556 SCV000225876 uncertain significance not provided 2014-05-21 criteria provided, single submitter clinical testing
Counsyl RCV000665382 SCV000789495 uncertain significance Usher syndrome, type 1C; Deafness, autosomal recessive 18 2017-02-02 criteria provided, single submitter clinical testing

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