ClinVar Miner

List of variants reported as pathogenic for Autosomal recessive nonsyndromic hearing loss 31

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_015404.4(WHRN):c.2332C>T (p.Arg778Ter)	rs137852839
NM_015404.4(WHRN):c.2423del (p.Gly808fs)	rs869320674
NM_015404.4(WHRN):c.26C>A (p.Ser9Ter)	rs776268964

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