ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.8083A>C (p.Lys2695Gln)

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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 RCV003881666 SCV004697318 uncertain significance Autosomal recessive nonsyndromic hearing loss 3 no assertion criteria provided clinical testing

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