ClinVar Miner

Submissions for variant NM_206933.3(USH2A):c.10613G>A (p.Arg3538Gln) (rs774844491)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Praxis fuer Humangenetik Tuebingen RCV000487925 SCV000574814 uncertain significance not provided 2016-09-30 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000487925 SCV000341149 uncertain significance not provided 2016-05-04 criteria provided, single submitter clinical testing
Human Genetics - Radboudumc,Radboudumc RCV000678642 SCV000804730 uncertain significance Cone-rod dystrophy 2016-09-01 no assertion criteria provided clinical testing

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