ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.5835T>G (p.Tyr1945Ter)

dbSNP: rs2142343642
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnosis Center for Deafness RCV002051752 SCV001984921 pathogenic Autosomal recessive nonsyndromic hearing loss 3 criteria provided, single submitter clinical testing
Deafness Molecular Diagnostic Center, Chinese PLA General Hospital RCV002051752 SCV001949934 likely pathogenic Autosomal recessive nonsyndromic hearing loss 3 no assertion criteria provided case-control

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