List of variants studied for autosomal recessive nonsyndromic hearing loss 3 by Baylor Genetics

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.1552G>A (p.Glu518Lys)	rs189255177	0.00105
NM_016239.4(MYO15A):c.1634C>T (p.Ala545Val)	rs199740747	0.00063
NM_016239.4(MYO15A):c.3622C>T (p.Arg1208Cys)	rs201618718	0.00063
NM_016239.4(MYO15A):c.4153T>G (p.Ser1385Ala)	rs201246214	0.00036
NM_016239.4(MYO15A):c.4976G>A (p.Arg1659Gln)	rs141473928	0.00035
NM_016239.4(MYO15A):c.10181C>T (p.Ala3394Val)	rs200249886	0.00024
NM_016239.4(MYO15A):c.5866C>T (p.Arg1956Trp)	rs185873402	0.00016
NM_016239.4(MYO15A):c.5867G>A (p.Arg1956Gln)	rs769596933	0.00006
NM_016239.4(MYO15A):c.2452C>A (p.Arg818Ser)	rs1424289379	0.00001
NM_016239.4(MYO15A):c.5962G>A (p.Glu1988Lys)	rs749019041	0.00001
NM_016239.4(MYO15A):c.4235T>A (p.Phe1412Tyr)	rs1597779977
NM_016239.4(MYO15A):c.823G>A (p.Gly275Ser)	rs183969516
NM_016239.4(MYO15A):c.8812G>A (p.Gly2938Arg)

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