ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.1977del (p.Gly660fs)

dbSNP: rs1555078942
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
NIHR Bioresource Rare Diseases, University of Cambridge RCV000504671 SCV000599115 likely pathogenic Usher syndrome 2015-01-01 no assertion criteria provided research

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