Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1064651
GBA
0.732 0.360 1 155235727 missense variant C/G snv 1.3E-04 2.0E-04 2
rs1553217009
GBA
0.882 0.120 1 155235757 missense variant C/T snv 2
rs364897
GBA
0.807 0.120 1 155238215 missense variant T/C snv 7.2E-05 1.0E-04 2
rs367968666
GBA
0.882 0.120 1 155237458 missense variant A/C snv 2.4E-04 1.6E-04 2
rs398123530
GBA
0.851 0.120 1 155238597 missense variant G/A snv 4.0E-06 2
rs409652
GBA
0.827 0.120 1 155238174 missense variant C/T snv 3.2E-05 2.1E-05 2
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 2
rs1057519357
GBA
1.000 0.120 1 155235792 missense variant G/A snv 1
rs1064644
GBA
0.807 0.120 1 155238192 missense variant A/G snv 8.0E-06 1
rs1141811
GBA
1.000 0.120 1 155239948 missense variant G/A snv 4.0E-06 1
rs1141814
GBA
0.925 0.120 1 155239934 missense variant G/A snv 2.8E-05 1.4E-05 1
rs1161552095
GBA
0.925 0.120 1 155236307 missense variant C/T snv 4.0E-06 1.4E-05 1
rs1178732315
GBA
0.882 0.240 1 155236381 missense variant A/G snv 1.4E-05 1
rs121908297
GBA
1.000 0.120 1 155238519 missense variant T/G snv 1
rs121908298
GBA
1.000 0.120 1 155237357 missense variant G/A snv 1
rs121908299
GBA
1.000 0.120 1 155238624 missense variant G/A snv 1
rs121908300
GBA
1.000 0.120 1 155238144 missense variant A/G snv 4.0E-06 1
rs121908301
GBA
1.000 0.120 1 155235057 missense variant C/T snv 1
rs121908302
GBA
1.000 0.120 1 155240033 missense variant C/A snv 1
rs121908304
GBA
1.000 0.120 1 155236416 missense variant C/A snv 1
rs121908307
GBA
1.000 0.120 1 155236261 missense variant C/G snv 4.0E-06 1
rs121908308
GBA
0.925 0.120 1 155236295 missense variant G/A;C snv 8.0E-06 1
rs121908311
GBA
0.827 0.120 1 155235823 missense variant C/T snv 1.6E-05 7.0E-06 1
rs121908312
GBA
0.925 0.120 1 155239716 missense variant C/G snv 1
rs121908314
GBA
1.000 0.120 1 155235841 missense variant G/C snv 1