ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.10585del (p.Leu3529fs)

dbSNP: rs2047052213
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Prof. Karen Avraham, Tel Aviv University RCV001265212 SCV001443269 pathogenic Autosomal recessive nonsyndromic hearing loss 3 2020-10-27 criteria provided, single submitter research Recessive, congenital SNHL

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