ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.4596+2_4596+3del

dbSNP: rs2142315894
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Deafness Molecular Diagnostic Center, Chinese PLA General Hospital RCV001823228 SCV001763604 pathogenic Autosomal recessive nonsyndromic hearing loss 3 no assertion criteria provided case-control

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