ClinVar Miner

List of variants reported as benign for Autosomal dominant nonsyndromic hearing loss 36

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Total variants: 13
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HGVS dbSNP gnomAD frequency
NM_138691.3(TMC1):c.-219A>G rs7026304 0.55869
NM_138691.3(TMC1):c.-468G>A rs7022441 0.53167
NM_138691.3(TMC1):c.45C>T (p.Asp15=) rs2589615 0.51851
NM_138691.3(TMC1):c.241G>A (p.Glu81Lys) rs1796993 0.21988
NM_138691.3(TMC1):c.-329C>A rs7856724 0.13978
NM_138691.3(TMC1):c.1713C>T (p.Phe571=) rs34532421 0.08866
NM_138691.3(TMC1):c.-540C>T rs112220638 0.02586
NM_138691.3(TMC1):c.*183A>G rs71507808 0.02514
NM_138691.3(TMC1):c.*106G>C rs79830675 0.01140
NM_138691.3(TMC1):c.*28A>C rs151157872 0.00779
NM_138691.3(TMC1):c.-275G>A rs58824091 0.00773
NM_138691.3(TMC1):c.421C>T (p.Arg141Trp) rs11143384 0.00691
NM_138691.3(TMC1):c.*156T>C rs545955592 0.00005

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