ClinVar Miner

Submissions for variant NM_001292063.2(OTOG):c.2695C>T (p.Gln899Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Cologne University RCV004549022 SCV005043280 pathogenic Autosomal recessive nonsyndromic hearing loss 18B 2024-03-13 criteria provided, single submitter clinical testing

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