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: rs104893915
rs104893915
0.776 0.200 5 149980428 missense variant C/T snv 9.8E-04 1.0E-03
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 6 1996 2010
dbSNP: rs104894094
rs104894094
0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 8 2000 2011
dbSNP: rs104894635
rs104894635
0.882 0.120 17 80213815 missense variant C/A;T snv 4.4E-06; 3.3E-04
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 8 2003 2018
dbSNP: rs104894639
rs104894639
0.925 0.120 17 80210622 missense variant C/T snv 6.8E-05 2.8E-05
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 8 2003 2018
dbSNP: rs1057519389
rs1057519389
0.695 0.400 10 129957324 missense variant C/A;G;T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 8 2009 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
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: 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: 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: 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: rs1085307993
rs1085307993
0.716 0.440 5 161331056 missense variant C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 0
dbSNP: rs1131691608
rs1131691608
1.000 X 41346503 splice acceptor variant A/G snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 16 1989 2017
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: rs1135402761
rs1135402761
0.827 0.320 12 79448958 missense variant T/C snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 0
dbSNP: rs113994048
rs113994048
1.000 0.040 3 184136734 missense variant A/T snv 4.4E-05 2.1E-05
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 5 1998 2014
dbSNP: rs1156904586
rs1156904586
1.000 13 25577115 frameshift variant -/T delins 1.4E-05
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 5 2012 2017
dbSNP: rs1161032867
rs1161032867
FUS
16 31191070 frameshift variant G/-;GGGG delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 7 2009 2015
dbSNP: rs118161496
rs118161496
1.000 0.040 14 31850092 non coding transcript exon variant T/C snv 3.4E-03 3.4E-03
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 14 1999 2013
dbSNP: rs119476050
rs119476050
1.000 0.080 14 50628154 missense variant C/T snv 4.0E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 3 2007 2013
dbSNP: rs1213060424
rs1213060424
X 70449787 stop gained C/A;T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 6 2004 2017
dbSNP: rs121434376
rs121434376
1.000 0.080 9 132327511 stop gained G/A snv 4.0E-06 7.0E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 4 2004 2009
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: rs121917995
rs121917995
2 165992368 missense variant C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 19 1997 2014
dbSNP: rs121918103
rs121918103
1.000 0.120 10 71828084 missense variant G/A snv 7.6E-05 1.4E-05
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 4 2005 2016
dbSNP: rs121918243
rs121918243
0.882 0.160 1 45508848 missense variant G/A snv 1.7E-04 7.7E-05
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 7 2006 2015