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: rs80338677
rs80338677
0.925 0.080 19 12655693 splice donor variant C/G snv 9.3E-05 7.7E-05
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 6 1981 2015
dbSNP: rs1554776842
rs1554776842
9 127660080 frameshift variant C/- delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 27 1998 2016
dbSNP: rs1554777375
rs1554777375
9 127665304 frameshift variant -/A delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 27 1998 2016
dbSNP: rs796053361
rs796053361
0.925 0.040 9 127668160 missense variant G/A;T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 27 1998 2016
dbSNP: rs1554777919
rs1554777919
9 127669950 frameshift variant G/- delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 27 1998 2016
dbSNP: rs767199598
rs767199598
9 127682451 stop gained C/A;T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 27 1998 2016
dbSNP: rs1554778941
rs1554778941
9 127682485 frameshift variant G/- delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 27 1998 2016
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: 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: rs1554820931
rs1554820931
9 132328198 frameshift variant -/T delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 4 2004 2009
dbSNP: rs1554822175
rs1554822175
9 132331387 frameshift variant A/- delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 4 2004 2009
dbSNP: rs587776537
rs587776537
1.000 0.080 9 132346304 inframe deletion AGA/- delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 4 2004 2009
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: rs782061187
rs782061187
1.000 9 133351945 frameshift variant -/A delins 4.0E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 7 1998 2016
dbSNP: rs1554768709
rs1554768709
1.000 9 133354824 missense variant C/G snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 7 1998 2016
dbSNP: rs1554260888
rs1554260888
1.000 6 133456594 frameshift variant A/- del
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 3 2005 2016
dbSNP: rs1556026984
rs1556026984
0.925 0.120 X 134475194 missense variant G/C snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 3 2014 2015
dbSNP: rs963172852
rs963172852
9 136418848 missense variant C/T snv 8.0E-06 2.1E-05
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 6 1998 2016
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: rs1555907034
rs1555907034
X 13760532 frameshift variant T/- delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 14 2000 2016
dbSNP: rs201337850
rs201337850
3 139348309 stop gained T/G snv 4.0E-06 7.0E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 5 2007 2017
dbSNP: rs1554129039
rs1554129039
1.000 5 140114334 frameshift variant A/- del
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 17 1991 2018
dbSNP: rs1554129113
rs1554129113
5 140114873 missense variant T/C snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 17 1991 2018
dbSNP: rs387906639
rs387906639
0.925 0.120 5 140674776 missense variant T/G snv 2.0E-05 9.1E-05
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 4 2012 2016
dbSNP: rs869025340
rs869025340
0.925 0.160 7 140777032 missense variant A/C;G;T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 8 1968 2013