ClinVar Miner

List of variants studied for peripheral vertigo

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 216
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HGVS dbSNP gnomAD frequency
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_001039141.3(TRIOBP):c.5588C>T (p.Ala1863Val) rs140528529 0.00203
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_000081.4(LYST):c.6710A>C (p.Gln2237Pro) rs138443479 0.00148
NM_001378778.1(MPDZ):c.2194T>A (p.Ser732Thr) rs200475640 0.00138
NM_002473.6(MYH9):c.4198C>T (p.Arg1400Trp) rs76368635 0.00123
NM_002334.4(LRP4):c.5660C>G (p.Ser1887Cys) rs149082597 0.00111
NM_001369268.1(ACAN):c.5567G>A (p.Ser1856Asn) rs200762388 0.00098
NM_001854.4(COL11A1):c.328G>C (p.Gly110Arg) rs141978499 0.00088
NM_001292063.2(OTOG):c.385G>A (p.Val129Met) rs552304627 0.00081
NM_002160.4(TNC):c.3196C>T (p.Arg1066Cys) rs139280264 0.00079
NM_004431.5(EPHA2):c.2162G>A (p.Arg721Gln) rs116506614 0.00073
NM_002470.4(MYH3):c.875C>G (p.Ser292Cys) rs139480342 0.00068
NM_001039141.3(TRIOBP):c.5014G>T (p.Gly1672Ter) rs200045032 0.00054
NM_002160.4(TNC):c.1297G>A (p.Asp433Asn) rs147990968 0.00052
NM_015978.3(TNNI3K):c.1528G>T (p.Val510Leu) rs34335537 0.00046
NM_018451.5(CPAP):c.2785A>G (p.Lys929Glu) rs141844033 0.00046
NM_002334.4(LRP4):c.4699A>T (p.Arg1567Trp) rs199747378 0.00041
NM_000260.4(MYO7A):c.2057G>A (p.Arg686His) rs781991817 0.00036
NM_001854.4(COL11A1):c.1427G>A (p.Arg476His) rs149558726 0.00036
NM_000642.3(AGL):c.854G>A (p.Arg285Gln) rs144817648 0.00026
NM_001369268.1(ACAN):c.836G>A (p.Arg279Gln) rs184913582 0.00026
NM_004999.4(MYO6):c.475G>A (p.Glu159Lys) rs201507590 0.00026
NM_002473.6(MYH9):c.4225G>A (p.Asp1409Asn) rs34292387 0.00025
NM_001852.4(COL9A2):c.1834G>A (p.Gly612Arg) rs142151614 0.00022
NM_000260.4(MYO7A):c.6247G>A (p.Ala2083Thr) rs41298759 0.00021
NM_005908.4(MANBA):c.1921C>T (p.Arg641Cys) rs140692906 0.00021
NM_006005.3(WFS1):c.2053C>T (p.Arg685Cys) rs112967046 0.00020
NM_001854.4(COL11A1):c.4594C>G (p.Pro1532Ala) rs140954784 0.00019
NM_006005.3(WFS1):c.1123C>T (p.Arg375Cys) rs200095753 0.00019
NM_032119.4(ADGRV1):c.16640G>A (p.Arg5547His) rs200907244 0.00017
NM_000092.5(COL4A4):c.1055C>T (p.Pro352Leu) rs371717486 0.00016
NM_001369268.1(ACAN):c.1948G>A (p.Val650Met) rs201414869 0.00015
NM_000642.3(AGL):c.4076G>A (p.Arg1359His) rs201533636 0.00014
NM_001145809.2(MYH14):c.526G>A (p.Ala176Thr) rs138001307 0.00014
NM_005908.4(MANBA):c.1499G>A (p.Arg500His) rs147542645 0.00014
NM_006005.3(WFS1):c.124C>T (p.Arg42Ter) rs71530923 0.00013
NM_022772.4(EPS8L2):c.13G>A (p.Gly5Arg) rs375020679 0.00012
NM_000081.4(LYST):c.3311G>A (p.Arg1104Gln) rs148299757 0.00011
NM_001148.6(ANK2):c.8144C>T (p.Ser2715Phe) rs147619875 0.00011
NM_001148.6(ANK2):c.10805G>A (p.Arg3602Gln) rs374991526 0.00010
NM_000642.3(AGL):c.3451C>T (p.Arg1151Trp) rs370797337 0.00009
NM_001365951.3(KIF1B):c.146C>A (p.Ser49Tyr) rs143654307 0.00009
NM_000092.5(COL4A4):c.4678C>T (p.Arg1560Cys) rs200973262 0.00008
NM_001080432.3(FTO):c.185A>G (p.His62Arg) rs550932456 0.00008
NM_005908.4(MANBA):c.1916G>A (p.Arg639His) rs536744758 0.00008
NM_018451.5(CPAP):c.1849C>T (p.Pro617Ser) rs573822147 0.00008
NM_018451.5(CPAP):c.659C>T (p.Ser220Leu) rs201219786 0.00008
NM_005422.4(TECTA):c.4481T>C (p.Val1494Ala) rs200544452 0.00007
NM_001378778.1(MPDZ):c.5183T>C (p.Leu1728Pro) rs772792353 0.00006
NM_001852.4(COL9A2):c.2059A>G (p.Lys687Glu) rs201847956 0.00006
NM_004341.5(CAD):c.2297T>C (p.Met766Thr) rs138025761 0.00006
NM_004999.4(MYO6):c.1589A>T (p.Asp530Val) rs373929865 0.00006
NM_005908.4(MANBA):c.1922G>A (p.Arg641His) rs569997475 0.00006
NM_022124.6(CDH23):c.6512G>A (p.Arg2171His) rs531513127 0.00006
NM_001378609.3(OTOGL):c.975del (p.Leu325fs) rs766753922 0.00005
NM_018451.5(CENPJ):c.1749A>C (p.Gln583His) rs746938343 0.00005
NM_000081.4(LYST):c.4705A>C (p.Asn1569His) rs767687843 0.00004
NM_000260.4(MYO7A):c.2507G>A (p.Arg836His) rs782179888 0.00004
NM_001145809.2(MYH14):c.3237G>T (p.Lys1079Asn) rs370658125 0.00004
NM_001145809.2(MYH14):c.4946G>A (p.Arg1649Gln) rs368076336 0.00004
NM_001364905.1(LRBA):c.109C>T (p.Pro37Ser) rs374519451 0.00004
NM_001364905.1(LRBA):c.319C>A (p.Gln107Lys) rs373476644 0.00004
NM_002470.4(MYH3):c.347A>G (p.Tyr116Cys) rs147024680 0.00004
NM_012418.4(FSCN2):c.65G>A (p.Arg22His) rs200258773 0.00004
NM_012418.4(FSCN2):c.733C>T (p.Arg245Ter) rs781864584 0.00004
NM_000081.4(LYST):c.10870G>A (p.Val3624Ile) rs776033238 0.00003
NM_001854.4(COL11A1):c.698A>G (p.Tyr233Cys) rs141304474 0.00003
NM_004341.5(CAD):c.3008A>G (p.Tyr1003Cys) rs367833212 0.00003
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_206996.4(SPAG17):c.1069G>C (p.Asp357His) rs183758503 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_000092.5(COL4A4):c.3434G>A (p.Gly1145Glu) rs1260916310 0.00001
NM_000092.5(COL4A4):c.4522G>A (p.Gly1508Ser) rs1003748020 0.00001
NM_000642.3(AGL):c.809G>A (p.Gly270Glu) rs1466350775 0.00001
NM_001148.6(ANK2):c.3979A>G (p.Met1327Val) rs778074732 0.00001
NM_001378778.1(MPDZ):c.4879G>A (p.Glu1627Lys) rs772598863 0.00001
NM_001386795.1(DTNA):c.2224G>T (p.Val742Phe) rs533568822 0.00001
NM_001854.4(COL11A1):c.2231A>G (p.Lys744Arg) rs775660447 0.00001
NM_002470.4(MYH3):c.787G>T (p.Asp263Tyr) rs771509347 0.00001
NM_015978.3(TNNI3K):c.1477C>T (p.Arg493Ter) rs201857576 0.00001
NM_015978.3(TNNI3K):c.1526A>T (p.Glu509Val) rs760008465 0.00001
NM_015978.3(TNNI3K):c.187C>T (p.Arg63Cys) rs79045456 0.00001
NC_000017.11:g.40356228C>T
NM_000081.4(LYST):c.116T>A (p.Met39Lys)
NM_000081.4(LYST):c.9314A>C (p.Lys3105Thr)
NM_000260.4(MYO7A):c.2617C>T (p.Arg873Trp) rs200454015
NM_000260.4(MYO7A):c.4635G>A (p.Trp1545Ter) rs918353878
NM_000642.3(AGL):c.1643C>T (p.Pro548Leu)
NM_001039141.3(TRIOBP):c.6560T>C (p.Leu2187Pro)
NM_001039141.3(TRIOBP):c.6911G>A (p.Arg2304Gln)
NM_001080432.3(FTO):c.1154A>C (p.Gln385Pro)
NM_001080432.3(FTO):c.287G>A (p.Arg96His) rs139577103
NM_001080477.4(TENM3):c.1847A>T (p.Asp616Val)
NM_001080477.4(TENM3):c.2065G>A (p.Gly689Ser)
NM_001080477.4(TENM3):c.3400G>A (p.Gly1134Arg)
NM_001080477.4(TENM3):c.5243A>G (p.Glu1748Gly)
NM_001080477.4(TENM3):c.5504G>A (p.Gly1835Asp)
NM_001080779.2(MYO1C):c.1232G>A (p.Trp411Ter)
NM_001080779.2(MYO1C):c.1316A>T (p.Asn439Ile)
NM_001080779.2(MYO1C):c.1351G>A (p.Glu451Lys)
NM_001080779.2(MYO1C):c.185C>T (p.Ala62Val)
NM_001080779.2(MYO1C):c.2252G>A (p.Arg751Gln)
NM_001080779.2(MYO1C):c.427G>A (p.Gly143Arg)
NM_001080779.2(MYO1C):c.775C>T (p.Arg259Trp)
NM_001128840.3(CACNA1D):c.1105G>A (p.Val369Met)
NM_001128840.3(CACNA1D):c.5848C>T (p.Pro1950Ser)
NM_001145809.2(MYH14):c.3931C>T (p.Arg1311Trp)
NM_001145809.2(MYH14):c.5921C>T (p.Ser1974Phe)
NM_001145809.2(MYH14):c.727G>C (p.Glu243Gln)
NM_001148.6(ANK2):c.37G>T (p.Gly13Ter)
NM_001148.6(ANK2):c.49A>G (p.Asn17Asp)
NM_001148.6(ANK2):c.7347C>G (p.His2449Gln)
NM_001177693.2(ARHGEF28):c.1027C>T (p.Arg343Cys)
NM_001177693.2(ARHGEF28):c.1865C>A (p.Thr622Asn)
NM_001177693.2(ARHGEF28):c.1982C>T (p.Ser661Phe)
NM_001177693.2(ARHGEF28):c.4172C>A (p.Thr1391Asn)
NM_001177693.2(ARHGEF28):c.4835T>C (p.Leu1612Pro)
NM_001292063.2(OTOG):c.2203C>A (p.Pro735Thr) rs2134027384
NM_001329752.2(FAM136A):c.547C>T (p.Gln183Ter) rs690016537
NM_001364905.1(LRBA):c.1348C>T (p.Leu450Phe)
NM_001364905.1(LRBA):c.4048A>T (p.Asn1350Tyr)
NM_001365951.3(KIF1B):c.4126C>T (p.Pro1376Ser)
NM_001365951.3(KIF1B):c.4675A>G (p.Thr1559Ala)
NM_001369268.1(ACAN):c.5726C>G (p.Ser1909Cys)
NM_001369268.1(ACAN):c.5756C>T (p.Ser1919Leu)
NM_001378609.3(OTOGL):c.1556C>T (p.Thr519Met)
NM_001378609.3(OTOGL):c.3413T>G (p.Ile1138Ser)
NM_001378609.3(OTOGL):c.3544G>A (p.Ala1182Thr)
NM_001378609.3(OTOGL):c.5145G>A (p.Trp1715Ter)
NM_001378778.1(MPDZ):c.1739C>G (p.Ser580Cys) rs149265684
NM_001378778.1(MPDZ):c.3583C>A (p.Pro1195Thr)
NM_001378778.1(MPDZ):c.4295A>T (p.Asn1432Ile)
NM_001378778.1(MPDZ):c.791G>A (p.Gly264Glu)
NM_001852.4(COL9A2):c.313G>A (p.Gly105Arg)
NM_001854.4(COL11A1):c.497G>T (p.Arg166Leu)
NM_002160.4(TNC):c.1873C>T (p.Pro625Ser)
NM_002160.4(TNC):c.2129C>T (p.Thr710Met)
NM_002160.4(TNC):c.2227G>A (p.Glu743Lys)
NM_002160.4(TNC):c.2512G>A (p.Gly838Ser)
NM_002160.4(TNC):c.2705T>A (p.Val902Asp)
NM_002160.4(TNC):c.608G>T (p.Gly203Val)
NM_002334.4(LRP4):c.1490T>G (p.Leu497Arg)
NM_002334.4(LRP4):c.2143C>T (p.Pro715Ser)
NM_002334.4(LRP4):c.860G>C (p.Trp287Ser)
NM_002470.4(MYH3):c.248C>G (p.Pro83Arg) rs199513213
NM_002470.4(MYH3):c.3104T>G (p.Leu1035Arg)
NM_002470.4(MYH3):c.5345G>A (p.Arg1782Gln)
NM_002470.4(MYH3):c.545G>C (p.Gly182Ala)
NM_003898.4(SYNJ2):c.1637G>A (p.Arg546Gln)
NM_003898.4(SYNJ2):c.179C>T (p.Ala60Val)
NM_003898.4(SYNJ2):c.1850G>A (p.Arg617His)
NM_003898.4(SYNJ2):c.559G>A (p.Gly187Arg)
NM_003898.4(SYNJ2):c.901G>A (p.Val301Met)
NM_004341.5(CAD):c.3494C>T (p.Ala1165Val)
NM_004341.5(CAD):c.5785G>A (p.Val1929Ile)
NM_004431.5(EPHA2):c.556G>A (p.Gly186Ser)
NM_004431.5(EPHA2):c.943C>T (p.Arg315Trp)
NM_004999.4(MYO6):c.1445A>G (p.Gln482Arg)
NM_004999.4(MYO6):c.883C>T (p.Arg295Cys)
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_006005.3(WFS1):c.1294C>G (p.Leu432Val) rs35031397
NM_012418.4(FSCN2):c.368C>T (p.Thr123Ile)
NM_012418.4(FSCN2):c.664A>G (p.Lys222Glu)
NM_014520.4(MYBBP1A):c.2407C>T (p.Arg803Cys)
NM_014520.4(MYBBP1A):c.2419C>T (p.Arg807Trp)
NM_014520.4(MYBBP1A):c.2551C>T (p.Pro851Ser)
NM_014520.4(MYBBP1A):c.2906T>A (p.Leu969Ter)
NM_014520.4(MYBBP1A):c.3349C>T (p.Gln1117Ter)
NM_015226.3(CLEC16A):c.1501G>A (p.Val501Met)
NM_015226.3(CLEC16A):c.2066C>T (p.Pro689Leu)
NM_015226.3(CLEC16A):c.913C>T (p.Arg305Trp)
NM_015978.3(TNNI3K):c.1389T>G (p.Ile463Met)
NM_018451.5(CENPJ):c.1220C>A (p.Ser407Tyr)
NM_018451.5(CENPJ):c.3538G>T (p.Glu1180Ter)
NM_018451.5(CENPJ):c.3539A>G (p.Glu1180Gly)
NM_018451.5(CPAP):c.3653C>T (p.Thr1218Met) rs149855336
NM_022065.5(THADA):c.2006A>G (p.Tyr669Cys)
NM_022065.5(THADA):c.2497G>A (p.Ala833Thr)
NM_022065.5(THADA):c.3715A>T (p.Ile1239Phe)
NM_022065.5(THADA):c.4911G>A (p.Trp1637Ter)
NM_022065.5(THADA):c.5293A>C (p.Thr1765Pro)
NM_022772.4(EPS8L2):c.1141C>T (p.Arg381Cys)
NM_022772.4(EPS8L2):c.805T>C (p.Phe269Leu)
NM_022772.4(EPS8L2):c.814C>T (p.Arg272Trp) rs766514830
NM_022772.4(EPS8L2):c.922C>T (p.Pro308Ser)
NM_024718.5(RABL6):c.1094C>T (p.Ser365Leu)
NM_024718.5(RABL6):c.1294C>T (p.Leu432=)
NM_024718.5(RABL6):c.842G>A (p.Gly281Asp)
NM_080683.3(PTPN13):c.1625A>G (p.Glu542Gly)
NM_080683.3(PTPN13):c.1931C>T (p.Pro644Leu)
NM_080683.3(PTPN13):c.4184T>G (p.Ile1395Ser)
NM_080683.3(PTPN13):c.7360G>A (p.Glu2454Lys)
NM_152219.4(GJD3):c.237C>A (p.Leu79=)
NM_152219.4(GJD3):c.522G>C (p.Pro174=)
NM_152219.4(GJD3):c.523C>T (p.His175Tyr)
NM_152219.4(GJD3):c.758G>C (p.Arg253Pro)
NM_153676.4(USH1C):c.1823C>G (p.Pro608Arg) rs41282932
NM_206996.4(SPAG17):c.1981del (p.Gln661fs)
NM_206996.4(SPAG17):c.2545T>G (p.Tyr849Asp)
NM_206996.4(SPAG17):c.508A>T (p.Lys170Ter)

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