ClinVar Miner

List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 3 by Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_016239.4(MYO15A):c.3622C>T (p.Arg1208Cys)	rs201618718	0.00063
NM_016239.4(MYO15A):c.5866C>T (p.Arg1956Trp)	rs185873402	0.00016
NM_016239.4(MYO15A):c.3620T>C (p.Ile1207Thr)	rs1365097671

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