ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.[6580C>T];[7124_7127del]

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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 RCV004689559 SCV005186170 pathogenic Autosomal recessive nonsyndromic hearing loss 3 2024-08-09 criteria provided, single submitter clinical testing

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