ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.4454T>C (p.Leu1485Pro)

dbSNP: rs751973078
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Hereditary Hearing Loss Research Unit, University of Madras RCV001249185 SCV001366121 likely pathogenic Autosomal recessive nonsyndromic hearing loss 3 criteria provided, single submitter case-control

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