ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.1267_1270del (p.Ser423fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Neuberg Centre For Genomic Medicine, NCGM RCV004547293 SCV005042735 likely pathogenic Autosomal recessive nonsyndromic hearing loss 2 criteria provided, single submitter clinical testing

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