ClinVar Miner

List of variants reported as likely benign for Autosomal dominant nonsyndromic hearing loss 56 by Department of Pathology and Laboratory Medicine, Sinai Health System

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002160.4(TNC):c.115G>A (p.Ala39Thr)	rs143586851	0.00021
NM_002160.4(TNC):c.5128A>G (p.Met1710Val)	rs201311843
NM_002160.4(TNC):c.625G>A (p.Asp209Asn)

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