ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.10183C>T (p.Leu3395Phe)

dbSNP: rs952306971
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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 RCV001822951 SCV001984901 uncertain significance Autosomal recessive nonsyndromic hearing loss 3 criteria provided, single submitter clinical testing
WangQJ Lab, Chinese People's Liberation Army General Hospital RCV001822951 SCV001762500 uncertain significance Autosomal recessive nonsyndromic hearing loss 3 2021-07-01 no assertion criteria provided clinical testing

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