Source: CLINVAR

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: rs80338680
rs80338680
1.000 0.080 19 12649932 missense variant G/A;C;T snv 2.3E-04; 4.0E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 6 1981 2015
dbSNP: rs5030869
rs5030869
0.882 0.120 X 154532990 missense variant C/A;T snv 5.5E-06; 1.9E-04 6.6E-05
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 5 1981 2008
dbSNP: rs786203983
rs786203983
1.000 19 49862188 missense variant C/A snv 4.2E-05
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 8 1982 2017
dbSNP: rs797045047
rs797045047
1.000 9 137162510 missense variant G/A;C snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 25 1983 2017
dbSNP: rs28929474
rs28929474
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 6 1983 2015
dbSNP: rs1554236054
rs1554236054
1.000 6 157201481 frameshift variant -/G delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 20 1984 2017
dbSNP: rs1064795935
rs1064795935
1.000 13 110181389 missense variant C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 18 1984 2015
dbSNP: rs1555302735
rs1555302735
13 110173899 splice donor variant C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 18 1984 2015
dbSNP: rs1555303010
rs1555303010
13 110176450 missense variant C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 18 1984 2015
dbSNP: rs917027829
rs917027829
1.000 5 150069942 stop gained G/A;T snv 4.0E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 13 1984 2014
dbSNP: rs121907960
rs121907960
1.000 0.120 15 72349148 inframe deletion GAA/- delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 11 1986 2011
dbSNP: rs587779406
rs587779406
1.000 0.120 15 72346552 synonymous variant G/A snv 8.0E-05 1.0E-04
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 11 1986 2011
dbSNP: rs1131691712
rs1131691712
19 13286952 frameshift variant -/A delins 4.2E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 46 1988 2017
dbSNP: rs1382415023
rs1382415023
SON
1.000 21 33554945 frameshift variant GAAA/- delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 28 1988 2016
dbSNP: rs1555899177
rs1555899177
SON
1.000 21 33554005 frameshift variant ACTC/- del
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 28 1988 2016
dbSNP: rs1064797245
rs1064797245
0.776 0.280 19 41970540 missense variant G/A snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 27 1988 2017
dbSNP: rs200891944
rs200891944
19 41981976 missense variant C/A;T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 27 1988 2017
dbSNP: rs606231435
rs606231435
0.827 0.240 19 41970539 missense variant C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 27 1988 2017
dbSNP: rs587783685
rs587783685
0.925 0.120 12 49032113 stop gained G/A snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 25 1988 2017
dbSNP: rs781139634
rs781139634
2 25235768 stop gained G/A snv 7.0E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 36 1989 2018
dbSNP: rs1555046615
rs1555046615
1.000 11 118503389 frameshift variant A/- del
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 22 1989 2017
dbSNP: rs1555047506
rs1555047506
11 118505003 frameshift variant GTTT/- delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 22 1989 2017
dbSNP: rs782297546
rs782297546
0.925 0.240 11 118473471 frameshift variant C/-;CC delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 22 1989 2017
dbSNP: rs1057521083
rs1057521083
0.925 0.200 2 199348709 missense variant G/A snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 21 1989 2017
dbSNP: rs1057519430
rs1057519430
0.925 X 41346946 missense variant C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 16 1989 2017