ClinVar Miner

Submissions for variant NM_006005.3(WFS1):c.2141A>G (p.Asn714Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Statistical Genetics, Columbia University RCV004810731 SCV005431518 likely pathogenic Autosomal dominant nonsyndromic hearing loss 2024-11-08 criteria provided, single submitter research

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