ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.488C>A (p.Ser163Ter)

dbSNP: rs773729617
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Diagnostics Services (NGS), CSIR - Centre For Cellular And Molecular Biology RCV000855723 SCV000998749 pathogenic Autosomal recessive nonsyndromic hearing loss 3 2019-10-10 criteria provided, single submitter clinical testing

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