ClinVar Miner

Submissions for variant NM_005422.4(TECTA):c.3338G>C (p.Gly1113Ala)

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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 RCV005055042 SCV005688800 uncertain significance Autosomal recessive nonsyndromic hearing loss 21 2025-02-06 criteria provided, single submitter clinical testing

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