List of variants studied for autosomal recessive nonsyndromic hearing loss 3 by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.8183G>A (p.Arg2728His)	rs184435771	0.00011
NM_016239.4(MYO15A):c.6764+2T>A	rs763975867	0.00009
NM_016239.4(MYO15A):c.4777G>A (p.Glu1593Lys)	rs376469502	0.00008
NM_016239.4(MYO15A):c.6046+1G>A	rs201978571	0.00005
NM_016239.4(MYO15A):c.10491+2T>C	rs1390498839	0.00001
NM_016239.4(MYO15A):c.4351G>A (p.Asp1451Asn)	rs767270134	0.00001
NM_016239.4(MYO15A):c.10247CCT[1] (p.Ser3417del)	rs760069953
NM_016239.4(MYO15A):c.1137del (p.Tyr380fs)	rs769260536
NM_016239.4(MYO15A):c.1185dup (p.Glu396fs)	rs772536599
NM_016239.4(MYO15A):c.5461del (p.Val1821fs)	rs764867438
NM_016239.4(MYO15A):c.7124_7127del (p.Asp2375fs)	rs780170125
NM_016239.4(MYO15A):c.8162C>A (p.Thr2721Lys)	rs1288328459
NM_016239.4(MYO15A):c.9371dup (p.Asn3124fs)	rs2046752611

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