ClinVar Miner

Submissions for variant NM_004568.6(SERPINB6):c.203T>C (p.Ile68Thr)

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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 Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV003990464 SCV004807133 uncertain significance Autosomal recessive nonsyndromic hearing loss 91 2024-03-26 criteria provided, single submitter clinical testing

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