ClinVar Miner

List of variants reported as pathogenic for Autosomal recessive nonsyndromic hearing loss 21 by National Institute on Deafness and Communication Disorders, National Institutes of Health

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_005422.4(TECTA):c.2736C>A (p.Cys912Ter)	rs368050948
NM_005422.4(TECTA):c.6162+5G>A	rs1565541888
NM_005422.4(TECTA):c.840_841insT (p.Val281fs)	rs1565519673

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