ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.1845del (p.Lys615fs) (rs886037762)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre de Biotechnologie de Sfax,Université de Sfax RCV000240660 SCV000257362 pathogenic Usher syndrome, type 1 2015-04-01 no assertion criteria provided research

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