ClinVar Miner

Submissions for variant NM_206933.3(USH2A):c.10585G>A (p.Gly3529Ser) (rs111033439)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000041674 SCV000065370 uncertain significance not specified 2009-08-03 criteria provided, single submitter clinical testing
Counsyl RCV000667791 SCV000792295 uncertain significance Usher syndrome, type 2A; Retinitis pigmentosa 39 2017-06-13 criteria provided, single submitter clinical testing

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