ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.9061C>T (p.Arg3021Ter)

dbSNP: rs1567658710
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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 RCV000678988 SCV000805204 likely pathogenic Autosomal recessive nonsyndromic hearing loss 3 2018-06-25 criteria provided, single submitter clinical testing

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