ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.8730C>A (p.Cys2910Ter)

dbSNP: rs776201118
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues RCV001533147 SCV001748966 pathogenic Autosomal recessive nonsyndromic hearing loss 3 2021-06-15 criteria provided, single submitter clinical testing

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