List of variants studied for Autosomal recessive nonsyndromic hearing loss 3 by Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.8767C>T (p.Arg2923Ter)	rs373462792	0.00005
NM_016239.4(MYO15A):c.6371G>A (p.Arg2124Gln)	rs368053088	0.00004
NM_016239.4(MYO15A):c.3844C>T (p.Arg1282Trp)	rs757155918	0.00001
NM_016239.4(MYO15A):c.4519C>T (p.Arg1507Ter)	rs549138385
NM_016239.4(MYO15A):c.5683G>A (p.Glu1895Lys)	rs2142341062

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