ClinVar Miner

List of variants in gene MYO6 reported as benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
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HGVS dbSNP
NM_004999.4(MYO6):c.*1287T>A
NM_004999.4(MYO6):c.*12C>T rs12606
NM_004999.4(MYO6):c.*1469G>T rs74367845
NM_004999.4(MYO6):c.*1607C>T rs77813459
NM_004999.4(MYO6):c.*1627A>G rs147347025
NM_004999.4(MYO6):c.*1703C>T rs9360957
NM_004999.4(MYO6):c.*1785A>C rs139803503
NM_004999.4(MYO6):c.*1962A>G rs80199115
NM_004999.4(MYO6):c.*2027T>C rs6914716
NM_004999.4(MYO6):c.*2547G>A rs148652044
NM_004999.4(MYO6):c.*2716A>G rs188568413
NM_004999.4(MYO6):c.*2910T>A rs140495245
NM_004999.4(MYO6):c.*2996A>G rs536099586
NM_004999.4(MYO6):c.*301G>A
NM_004999.4(MYO6):c.*3296G>T rs7741414
NM_004999.4(MYO6):c.*3447A>C rs1341567
NM_004999.4(MYO6):c.*3509G>A rs78129547
NM_004999.4(MYO6):c.*350T>C rs699186
NM_004999.4(MYO6):c.*3546A>G rs73751758
NM_004999.4(MYO6):c.*3632T>G rs9443200
NM_004999.4(MYO6):c.*3835C>T rs7742137
NM_004999.4(MYO6):c.*3879G>A rs189646143
NM_004999.4(MYO6):c.*3914T>C
NM_004999.4(MYO6):c.*3940T>C rs11964034
NM_004999.4(MYO6):c.*4114T>A rs7766661
NM_004999.4(MYO6):c.*4283A>G rs7746476
NM_004999.4(MYO6):c.*4283A>T rs7746476
NM_004999.4(MYO6):c.*4446A>G
NM_004999.4(MYO6):c.*4464C>T rs79815348
NM_004999.4(MYO6):c.*4481T>C rs142744723
NM_004999.4(MYO6):c.*459A>G rs1045758
NM_004999.4(MYO6):c.*875C>T rs184099248
NM_004999.4(MYO6):c.-49C>G rs149130280
NM_004999.4(MYO6):c.1025C>T (p.Ala342Val) rs145564837
NM_004999.4(MYO6):c.1120T>C (p.Tyr374His) rs61732664
NM_004999.4(MYO6):c.1176A>G (p.Thr392=) rs2273857
NM_004999.4(MYO6):c.1656G>A (p.Lys552=) rs111033431
NM_004999.4(MYO6):c.1674+13A>G rs6925845
NM_004999.4(MYO6):c.1722C>T (p.Asp574=) rs11756446
NM_004999.4(MYO6):c.2534C>T (p.Thr845Ile) rs55662069
NM_004999.4(MYO6):c.2595C>T (p.Pro865=) rs150876010
NM_004999.4(MYO6):c.262-9C>T rs187811833
NM_004999.4(MYO6):c.2982G>A (p.Glu994=) rs55905349
NM_004999.4(MYO6):c.3246T>C (p.Tyr1082=) rs138437852
NM_004999.4(MYO6):c.3303C>T (p.Cys1101=) rs9443199
NM_004999.4(MYO6):c.3333G>A (p.Val1111=) rs114970874
NM_004999.4(MYO6):c.3563A>G (p.Lys1188Arg) rs61734891
NM_004999.4(MYO6):c.3667G>A (p.Asp1223Asn) rs41269323
NM_004999.4(MYO6):c.3824A>G (p.Tyr1275Cys) rs146461956
NM_004999.4(MYO6):c.475G>A (p.Glu159Lys) rs201507590
NM_004999.4(MYO6):c.553+11T>C rs12210963
NM_004999.4(MYO6):c.647A>T (p.Glu216Val) rs121912559

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