ClinVar Miner

Submissions for variant NM_004999.4(MYO6):c.560del (p.Pro187fs)

dbSNP: rs2150249865
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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 Medical Genetics and Applied Genomics, University Hospital Tübingen RCV002226798 SCV002505659 pathogenic Autosomal dominant nonsyndromic hearing loss 2022-05-02 criteria provided, single submitter clinical testing

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