ClinVar Miner

List of variants in gene MYO6 reported as benign for Autosomal dominant nonsyndromic hearing loss 22

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Gene type:
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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_004999.4(MYO6):c.817-21G>A rs7760587 0.99214
NM_004999.4(MYO6):c.*4114T>A rs7766661 0.71424
NM_004999.4(MYO6):c.*3835C>T rs7742137 0.51984
NM_004999.4(MYO6):c.*2027T>C rs6914716 0.39479
NM_004999.4(MYO6):c.*350T>C rs699186 0.33974
NM_004999.4(MYO6):c.*3940T>C rs11964034 0.33693
NM_004999.4(MYO6):c.2658+17C>T rs2295936 0.22603
NM_004999.4(MYO6):c.*12C>T rs12606 0.22544
NM_004999.4(MYO6):c.*3296G>T rs7741414 0.21429
NM_004999.4(MYO6):c.*3447A>C rs1341567 0.18060
NM_004999.4(MYO6):c.553+11T>C rs12210963 0.13246
NM_004999.4(MYO6):c.*459A>G rs1045758 0.13207
NM_004999.4(MYO6):c.1722C>T (p.Asp574=) rs11756446 0.04192
NM_004999.4(MYO6):c.*1703C>T rs9360957 0.03977
NM_004999.4(MYO6):c.3303C>T (p.Cys1101=) rs9443199 0.02151
NM_004999.4(MYO6):c.-49C>G rs149130280 0.01849
NM_004999.4(MYO6):c.*3546A>G rs73751758 0.01688
NM_004999.4(MYO6):c.*1962A>G rs80199115 0.01663
NM_004999.4(MYO6):c.1176A>G (p.Thr392=) rs2273857 0.01287
NM_004999.4(MYO6):c.*1469G>T rs74367845 0.01285
NM_004999.4(MYO6):c.*2547G>A rs148652044 0.01219
NM_004999.4(MYO6):c.*875C>T rs184099248 0.01168
NM_004999.4(MYO6):c.*3632T>G rs9443200 0.01023
NM_004999.4(MYO6):c.*3509G>A rs78129547 0.00972
NM_004999.4(MYO6):c.3667G>A (p.Asp1223Asn) rs41269323 0.00799
NM_004999.4(MYO6):c.*4464C>T rs79815348 0.00798
NM_004999.4(MYO6):c.1120T>C (p.Tyr374His) rs61732664 0.00762
NM_004999.4(MYO6):c.*2910T>A rs140495245 0.00749
NM_004999.4(MYO6):c.2982G>A (p.Glu994=) rs55905349 0.00487
NM_004999.4(MYO6):c.3333G>A (p.Val1111=) rs114970874 0.00471
NM_004999.4(MYO6):c.3246T>C (p.Tyr1082=) rs138437852 0.00470
NM_004999.4(MYO6):c.1656G>A (p.Lys552=) rs111033431 0.00448
NM_004999.4(MYO6):c.3824A>G (p.Tyr1275Cys) rs146461956 0.00424
NM_004999.4(MYO6):c.1674+13A>G rs6925845 0.00415
NM_004999.4(MYO6):c.*2716A>G rs188568413 0.00357
NM_004999.4(MYO6):c.*1607C>T rs77813459 0.00356
NM_004999.4(MYO6):c.*4481T>C rs142744723 0.00334
NM_004999.4(MYO6):c.2534C>T (p.Thr845Ile) rs55662069 0.00322
NM_004999.4(MYO6):c.*1287T>A rs570884031 0.00292
NM_004999.4(MYO6):c.3563A>G (p.Lys1188Arg) rs61734891 0.00266
NM_004999.4(MYO6):c.*1627A>G rs147347025 0.00263
NM_004999.4(MYO6):c.*3914T>C rs541767003 0.00228
NM_004999.4(MYO6):c.*301G>A rs116215208 0.00173
NM_004999.4(MYO6):c.2595C>T (p.Pro865=) rs150876010 0.00124
NM_004999.4(MYO6):c.*1785A>C rs139803503 0.00120
NM_004999.4(MYO6):c.*3879G>A rs189646143 0.00105
NM_004999.4(MYO6):c.*4446A>G rs148227849 0.00029
NM_004999.4(MYO6):c.*2996A>G rs536099586 0.00021
NM_004999.4(MYO6):c.262-9C>T rs187811833 0.00021
NM_004999.4(MYO6):c.*4283A>G rs7746476
NM_004999.4(MYO6):c.*4283A>T rs7746476

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