ClinVar Miner

Submissions for variant NM_016239.4(MYO15A):c.2061_2062insT (p.Pro688fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre RCV004821086 SCV005441999 likely pathogenic Autosomal recessive nonsyndromic hearing loss 3 2024-12-19 criteria provided, single submitter clinical testing

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