NM_001292063.2(OTOG):c.769G>A (p.Val257Ile)
|
rs61978648
|
0.02169
|
NM_000260.4(MYO7A):c.6640G>A (p.Gly2214Ser)
|
rs111033231
|
0.01911
|
NM_001292063.2(OTOG):c.8490G>C (p.Lys2830Asn)
|
rs61997203
|
0.01716
|
NM_001292063.2(OTOG):c.4606C>T (p.Leu1536Phe)
|
rs117380920
|
0.00806
|
NM_022124.6(CDH23):c.3845A>G (p.Asn1282Ser)
|
rs149073355
|
0.00347
|
NM_001292063.2(OTOG):c.3683C>T (p.Pro1228Leu)
|
rs117005078
|
0.00338
|
NM_001292063.2(OTOG):c.7631G>A (p.Arg2544Gln)
|
rs76461792
|
0.00308
|
NM_001292063.2(OTOG):c.4022G>A (p.Arg1341Gln)
|
rs145689709
|
0.00242
|
NM_001649.4(SHROOM2):c.631G>A (p.Gly211Ser)
|
rs138558321
|
0.00238
|
NM_001292063.2(OTOG):c.6074C>T (p.Ala2025Val)
|
rs61736002
|
0.00229
|
NM_032119.4(ADGRV1):c.7582C>T (p.Pro2528Ser)
|
rs201733037
|
0.00228
|
NM_001292063.2(OTOG):c.8369G>A (p.Arg2790His)
|
rs117315845
|
0.00188
|
NM_000260.4(MYO7A):c.1007G>A (p.Arg336His)
|
rs45629132
|
0.00164
|
NM_001292063.2(OTOG):c.385G>A (p.Val129Met)
|
rs552304627
|
0.00081
|
NM_000260.4(MYO7A):c.2057G>A (p.Arg686His)
|
rs781991817
|
0.00036
|
NM_000260.4(MYO7A):c.6247G>A (p.Ala2083Thr)
|
rs41298759
|
0.00021
|
NM_032119.4(ADGRV1):c.16640G>A (p.Arg5547His)
|
rs200907244
|
0.00017
|
NM_005422.4(TECTA):c.4481T>C (p.Val1494Ala)
|
rs200544452
|
0.00007
|
NM_022124.6(CDH23):c.6512G>A (p.Arg2171His)
|
rs531513127
|
0.00006
|
NM_000260.4(MYO7A):c.2507G>A (p.Arg836His)
|
rs782179888
|
0.00004
|
NM_005422.4(TECTA):c.4205G>C (p.Cys1402Ser)
|
rs774697277
|
0.00003
|
NM_033056.4(PCDH15):c.5236C>A (p.Pro1746Thr)
|
rs762526774
|
0.00003
|
NM_000260.4(MYO7A):c.3G>A (p.Met1Ile)
|
rs782787126
|
0.00002
|
NM_000260.4(MYO7A):c.6626G>A (p.Arg2209Gln)
|
rs776881443
|
0.00002
|
NM_001386795.1(DTNA):c.2224G>T (p.Val742Phe)
|
rs533568822
|
0.00001
|
NM_000260.4(MYO7A):c.2617C>T (p.Arg873Trp)
|
rs200454015
|
|
NM_000260.4(MYO7A):c.4635G>A (p.Trp1545Ter)
|
rs918353878
|
|
NM_001292063.2(OTOG):c.2203C>A (p.Pro735Thr)
|
rs2134027384
|
|
NM_001329752.2(FAM136A):c.547C>T (p.Gln183Ter)
|
rs690016537
|
|
NM_005422.4(TECTA):c.4422del (p.Asn1474fs)
|
rs2135120291
|
|
NM_005422.4(TECTA):c.5368C>T (p.Pro1790Ser)
|
rs1300740898
|
|
NM_005422.4(TECTA):c.6353del (p.Gly2118fs)
|
rs1223512271
|
|
NM_153676.4(USH1C):c.1823C>G (p.Pro608Arg)
|
rs41282932
|
|