ClinVar Miner

Submissions for variant NM_006383.4(CIB2):c.199-1G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Department of Human Genetics, Hannover Medical School RCV003227457 SCV003924015 likely pathogenic Autosomal recessive nonsyndromic hearing loss 48 2023-05-10 criteria provided, single submitter clinical testing

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