ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.5055dup (p.Asn1686fs)

dbSNP: rs1555543836
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Division of Human Genetics, Children's Hospital of Philadelphia RCV000477926 SCV000536902 likely pathogenic Autosomal recessive nonsyndromic hearing loss 3 2016-06-29 no assertion criteria provided research

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