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: rs1085307993
rs1085307993
0.716 0.440 5 161331056 missense variant C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 0
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: rs137852695
rs137852695
0.925 0.120 1 40091398 missense variant T/A snv 7.0E-04 6.0E-04
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 0
dbSNP: rs143657539
rs143657539
1 40092054 missense variant C/T snv 4.0E-06 1.4E-05
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 0
dbSNP: rs144900171
rs144900171
0.925 12 79448968 missense variant C/G;T snv 1.3E-04 6.2E-04
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 0
dbSNP: rs1554504663
rs1554504663
0.851 0.080 8 23007627 missense variant G/A snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 0
dbSNP: rs1555119899
rs1555119899
0.925 0.240 11 108326149 missense variant G/C snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 0
dbSNP: rs1565922388
rs1565922388
0.925 12 79353599 missense variant T/A snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 0
dbSNP: rs1565922395
rs1565922395
0.925 12 79353602 missense variant A/G snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 0
dbSNP: rs1565962725
rs1565962725
0.925 12 79448953 missense variant C/A snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 0
dbSNP: rs369691608
rs369691608
1.000 0.160 2 218661255 missense variant C/T snv 8.0E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 0
dbSNP: rs421016
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 0
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: rs1553597538
rs1553597538
2 218662571 frameshift variant CT/- delins
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 5 2001 2009
dbSNP: rs377025174
rs377025174
2 218661192 missense variant C/A;T snv 4.0E-06; 6.8E-05
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 5 2001 2009
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: rs1555511101
rs1555511101
GAN
16 81354554 stop gained C/G snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 4 1990 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: rs759581558
rs759581558
GAN
1.000 0.080 16 81356957 missense variant G/A snv 8.0E-06 7.0E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 4 1990 2009
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: 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: rs80359541
rs80359541
0.882 0.200 13 32340183 frameshift variant C/- del 8.0E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0.700 1.000 10 1998 2011