ClinVar Miner

Submissions for variant NM_004999.4(MYO6):c.1473_1473+2delinsC

dbSNP: rs878853225
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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 RCV000225059 SCV000281979 pathogenic Autosomal dominant nonsyndromic hearing loss 22 2016-02-16 no assertion criteria provided research Childhood onset, moderate-profound HL

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