List of variants reported as likely benign for Autosomal recessive nonsyndromic hearing loss 3 by Illumina Laboratory Services, Illumina

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.7503G>A (p.Thr2501=)	rs16960961	0.02872
NM_016239.4(MYO15A):c.4533C>T (p.Ala1511=)	rs114328138	0.01906
NM_016239.4(MYO15A):c.3413A>G (p.Gln1138Arg)	rs76468019	0.01903
NM_016239.4(MYO15A):c.9708G>A (p.Val3236=)	rs115393178	0.01622
NM_016239.4(MYO15A):c.1791G>A (p.Ala597=)	rs114552047	0.01041
NM_016239.4(MYO15A):c.6796G>A (p.Val2266Met)	rs114274755	0.00791
NM_016239.4(MYO15A):c.2028C>A (p.Pro676=)	rs577023485	0.00762
NM_016239.4(MYO15A):c.1385G>A (p.Gly462Asp)	rs145292219	0.00326
NM_016239.4(MYO15A):c.10573A>G (p.Ser3525Gly)	rs182332665	0.00151
NM_016239.4(MYO15A):c.7908C>T (p.Ala2636=)	rs201535856	0.00118
NM_016239.4(MYO15A):c.*628C>G	rs55973639

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