Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1447313633
rs1447313633
1.000 2 218649090 frameshift variant TT/- del
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 1.000 1 2019 2019
dbSNP: rs1559296368
rs1559296368
1.000 2 218646330 frameshift variant C/- del
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 1.000 1 2019 2019
dbSNP: rs1569151872
rs1569151872
0.851 0.240 21 44509225 frameshift variant GAC/AA delins
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 1.000 1 2016 2016
dbSNP: rs531630376
rs531630376
1.000 0.080 5 141955844 stop gained C/A snv 4.0E-06
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 1.000 1 2019 2019
dbSNP: rs546151500
rs546151500
0.925 0.080 2 218643341 stop gained G/A;T snv 8.0E-06; 4.0E-06
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 1.000 1 2019 2019
dbSNP: rs63750687
rs63750687
0.752 0.200 14 73217137 missense variant C/A;G;T snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 1.000 1 2014 2014
dbSNP: rs748787734
rs748787734
0.827 0.240 19 6495437 missense variant G/A;C snv 1.2E-05
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 1.000 1 2014 2014
dbSNP: rs797045055
rs797045055
CYTB ; ND5 ; ND6
1.000 0.080 MT 14597 missense variant A/G snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 1.000 1 2016 2016
dbSNP: rs879253799
rs879253799
0.882 0.320 2 171443559 frameshift variant A/- delins
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 1.000 1 2016 2016
dbSNP: rs1057518942
rs1057518942
1.000 0.160 18 23544424 missense variant G/A snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs1085307993
rs1085307993
0.716 0.440 5 161331056 missense variant C/T snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs1114167290
rs1114167290
0.882 0.080 15 52340235 missense variant G/C snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs1131692231
rs1131692231
0.827 0.280 5 157294834 missense variant C/T snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs113371321
rs113371321
18 23534477 missense variant G/A;C snv 1.2E-04
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs1135401746
rs1135401746
0.827 0.400 1 1806512 missense variant C/G snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs114925667
rs114925667
0.672 0.520 3 132675903 missense variant G/A;T snv 1.9E-03; 4.1E-06
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs121917762
rs121917762
TH
0.925 0.040 11 2165727 stop gained G/A;T snv 4.0E-06; 4.0E-06
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs137852968
rs137852968
0.925 0.080 20 3916955 stop gained C/A;T snv 4.0E-06; 1.2E-05; 3.6E-05
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs1553547838
rs1553547838
0.925 0.280 2 199328709 stop gained G/A snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs1553621496
rs1553621496
0.677 0.440 2 209976305 splice donor variant T/G snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs1553770577
rs1553770577
0.724 0.480 3 132675342 missense variant T/C snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs1554208945
rs1554208945
0.752 0.240 6 87260207 missense variant A/C snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs1554317002
rs1554317002
0.724 0.440 7 39950821 frameshift variant C/- delins
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs1554389088
rs1554389088
0.807 0.160 7 44243526 missense variant G/A snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0
dbSNP: rs1554504663
rs1554504663
0.851 0.080 8 23007627 missense variant G/A snv
CUI: C0013421
Disease: Dystonia
Dystonia
0.700 0