Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35749011 0.925 0.080 1 155162560 intergenic variant G/A snv 1.1E-02 2
rs75822236
GBA
0.752 0.200 1 155235002 missense variant C/T snv 1.8E-04 6.1E-05 10
rs80356771
GBA
0.776 0.160 1 155235196 missense variant G/A;T snv 7.2E-05; 4.0E-06 8
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs77369218
GBA
0.807 0.160 1 155235726 missense variant T/A snv 7
rs1064651
GBA
0.732 0.360 1 155235727 missense variant C/G snv 1.3E-04 2.0E-04 13
rs80356769
GBA
0.776 0.160 1 155235772 missense variant C/A snv 3.2E-05 7.0E-06 8
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs78973108
GBA
0.776 0.160 1 155237453 missense variant C/T snv 2.8E-05 4.2E-05 8
rs104886460
GBA
0.776 0.160 1 155240629 splice donor variant C/A;T snv 7.6E-05 8
rs12734374 1.000 0.080 1 155419060 intron variant A/T snv 3.4E-02 2
rs377591051 0.851 0.080 6 162262651 missense variant C/T snv 4.0E-06 7.0E-06 4
rs104893937 0.851 0.120 5 176621218 missense variant G/T snv 1.7E-04 2.0E-04 4
rs104893936 0.851 0.120 5 176626472 missense variant C/G;T snv 5.6E-05 4
rs113388242 0.925 0.080 3 184327376 missense variant C/T snv 4.0E-05 7.0E-05 3
rs112176450 0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 7
rs774457232 0.925 0.080 3 184331303 missense variant G/A;T snv 6.4E-05 3
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1041833271
APP
0.925 0.080 21 25975995 missense variant C/T snv 7.0E-06 2
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs897984 0.925 0.080 16 30875322 non coding transcript exon variant T/C snv 0.62 0.47 2
rs7308720 0.790 0.120 12 40263898 missense variant C/A;G snv 4.0E-06; 8.7E-02 7
rs7133914 0.790 0.120 12 40309109 missense variant G/A;T snv 8.5E-02; 1.6E-05 7