ClinVar Miner

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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