ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.625G>T (p.Glu209Ter)

dbSNP: rs571594379
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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 RCV000477946 SCV000536851 pathogenic Autosomal recessive nonsyndromic hearing loss 3 2016-02-26 no assertion criteria provided research

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