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: rs1064796453
rs1064796453
3 41235799 stop gained C/A;T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 22 1991 2017
dbSNP: rs1553631783
rs1553631783
3 41233416 frameshift variant G/- delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 22 1991 2017
dbSNP: rs1553732126
rs1553732126
3 123347875 frameshift variant -/G delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 22 1992 2017
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: rs1555764170
rs1555764170
18 55254579 frameshift variant CC/- del
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 22 2007 2017
dbSNP: rs775104326
rs775104326
0.776 0.160 3 41224995 stop gained C/A;T snv 4.0E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 22 1991 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: rs864309483
rs864309483
0.851 0.080 3 123352464 missense variant G/A snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 22 1992 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: rs1413339367
rs1413339367
1 42930661 stop gained G/A snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 21 1991 2016
dbSNP: rs1553156053
rs1553156053
1.000 1 42929652 stop gained G/A snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 21 1991 2016
dbSNP: rs1553317028
rs1553317028
1.000 2 32128440 inframe deletion CTT/- delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 21 1999 2016
dbSNP: rs1554086554
rs1554086554
5 114404815 inframe deletion TAT/- delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 21 1999 2016
dbSNP: rs1555254256
rs1555254256
1.000 13 23354906 stop gained C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 21 1993 2016
dbSNP: rs1557082399
rs1557082399
1.000 X 77593803 stop gained C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 21 1992 2017
dbSNP: rs797044850
rs797044850
1.000 0.080 2 32127017 missense variant A/G snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 21 1999 2016
dbSNP: rs878854991
rs878854991
0.882 0.080 2 32141906 missense variant G/A snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 21 1999 2016
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: rs1554599036
rs1554599036
1.000 8 60828698 frameshift variant GAACACTGTGGAAGAAC/- del
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 20 1999 2016
dbSNP: rs1555050165
rs1555050165
0.925 0.200 11 105926814 missense variant A/G snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 20 1992 2016
dbSNP: rs587777429
rs587777429
1.000 0.120 19 6496032 missense variant C/A;T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 20 2002 2017
dbSNP: rs74315402
rs74315402
0.882 0.200 20 4699570 missense variant C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 20 1993 2018
dbSNP: rs886041166
rs886041166
1.000 8 60742366 stop gained C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 20 1999 2016
dbSNP: rs121917995
rs121917995
2 165992368 missense variant C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 19 1997 2014