ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.3233G>A (p.Trp1078Ter)

dbSNP: rs866595552
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Testing Center for Deafness, Department of Otolaryngology Head & Neck Surgery, Institute of Otolaryngology, Chinese PLA General Hospital RCV000770838 SCV000902339 likely pathogenic Autosomal recessive nonsyndromic hearing loss 3 2019-02-26 no assertion criteria provided case-control

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