List of variants studied for autosomal recessive nonsyndromic hearing loss 3 by Division of Human Genetics, Children's Hospital of Philadelphia

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.1196A>G (p.Tyr399Cys)	rs368682932	0.00033
NM_016239.4(MYO15A):c.7367C>G (p.Ala2456Gly)	rs199953758	0.00015
NM_016239.4(MYO15A):c.10054G>A (p.Ala3352Thr)	rs367863299	0.00013
NM_016239.4(MYO15A):c.6580C>T (p.Arg2194Trp)	rs773551819	0.00011
NM_016239.4(MYO15A):c.4848C>G (p.Phe1616Leu)	rs368430972	0.00006
NM_016239.4(MYO15A):c.8714-1G>A	rs377015931	0.00006
NM_016239.4(MYO15A):c.5925G>A (p.Trp1975Ter)	rs375290498	0.00005
NM_016239.4(MYO15A):c.1721G>C (p.Arg574Pro)	rs964336018	0.00001
NM_016239.4(MYO15A):c.3311dup (p.Gly1104_Glu1105insTer)	rs794729637
NM_016239.4(MYO15A):c.5055dup (p.Asn1686fs)	rs1555543836
NM_016239.4(MYO15A):c.625G>T (p.Glu209Ter)	rs571594379

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