ClinVar Miner

List of variants reported as pathogenic for autosomal dominant nonsyndromic hearing loss 56

Included ClinVar conditions (1):

Autosomal dominant nonsyndromic hearing loss 56

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Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002160.4(TNC):c.5317G>A (p.Val1773Met)	rs137933052	0.00025
NM_002160.4(TNC):c.5247A>T (p.Gly1749=)
NM_002160.4(TNC):c.5386A>T (p.Thr1796Ser)	rs431905513

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