ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.257A>T (p.Gln86Leu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV003881686 SCV004697363 uncertain significance Usher syndrome type 2A no assertion criteria provided clinical testing

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