Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs377325220
GBA
1.000 0.120 1 155238621 missense variant T/C snv 8.0E-06 1
rs381427
GBA
1.000 0.120 1 155238206 missense variant A/C;T snv 1.2E-05 1
rs397518433
GBA
1.000 0.120 1 155240672 frameshift variant G/- delins 1
rs398123526
GBA
0.925 0.120 1 155236409 missense variant C/G;T snv 1.2E-05; 4.0E-06 1
rs398123528
GBA
1.000 0.120 1 155235829 missense variant C/A;G snv 4.0E-06 1
rs74462743
GBA
0.925 0.120 1 155238194 missense variant C/T snv 8.0E-06 1
rs74598136
GBA
0.925 0.120 1 155235750 missense variant G/A snv 1
rs74731340
GBA
1.000 0.120 1 155237411 missense variant C/T snv 1
rs74752878
GBA
1.000 0.120 1 155235699 missense variant T/C snv 1
rs749416070
GBA
1.000 0.120 1 155238269 missense variant C/G;T snv 4.3E-05 1
rs74979486
GBA
1.000 0.120 1 155236276 missense variant C/T snv 7.0E-06 1
rs75243000
GBA
1.000 0.120 1 155235762 missense variant A/G snv 1
rs75385858
GBA
1.000 0.120 1 155235765 missense variant T/G snv 1
rs75528494
GBA
1.000 0.120 1 155236254 missense variant G/C;T snv 1
rs75548401
GBA
0.882 0.160 1 155236246 missense variant G/A snv 5.9E-03 6.2E-03 1
rs75564605
GBA
1.000 0.120 1 155235747 missense variant A/G snv 1
rs757041827
GBA
1.000 0.120 1 155240641 missense variant G/A;C snv 2.0E-05; 8.0E-06 1
rs76026102
GBA
1.000 0.120 1 155238164 missense variant T/C snv 4.0E-06 1
rs76071730
GBA
1.000 0.120 1 155235231 missense variant T/C;G snv 1.2E-05 1
rs76228122
GBA
1.000 0.120 1 155236264 missense variant T/C snv 1
rs76500263
GBA
1.000 0.120 1 155238293 missense variant T/G snv 1
rs765633380
GBA
1.000 0.120 1 155237370 missense variant G/A snv 2.0E-05 7.0E-06 1
rs76725886
GBA
0.925 0.120 1 155237531 missense variant G/A;C snv 4.0E-06 1
rs76910485
GBA
1.000 0.120 1 155235780 missense variant G/A snv 1
rs772548282
GBA
1.000 0.120 1 155235798 missense variant A/G snv 1