ClinVar Miner

Submissions for variant NM_000260.4(MYO7A):c.736-2A>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Medical Molecular Genetics Department, National Research Center RCV005055232 SCV005184327 likely pathogenic Autosomal recessive nonsyndromic hearing loss 2 2024-01-02 criteria provided, single submitter clinical testing

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