Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs777296100 0.925 0.080 4 89725318 3 prime UTR variant -/TAA;TAAAA ins 2
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs2306604 0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs12734374 1.000 0.080 1 155419060 intron variant A/T snv 3.4E-02 2
rs1446915570 0.925 0.080 14 73173623 synonymous variant A/T snv 4.0E-06 7.0E-06 2
rs80356769
GBA
0.776 0.160 1 155235772 missense variant C/A snv 3.2E-05 7.0E-06 8
rs7308720 0.790 0.120 12 40263898 missense variant C/A;G snv 4.0E-06; 8.7E-02 7
rs7681440 1.000 0.080 4 89835399 intron variant C/A;G snv 1
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs104886460
GBA
0.776 0.160 1 155240629 splice donor variant C/A;T snv 7.6E-05 8
rs104893878 0.732 0.160 4 89835580 missense variant C/G snv 21
rs1064651
GBA
0.732 0.360 1 155235727 missense variant C/G snv 1.3E-04 2.0E-04 13
rs72824905 0.827 0.200 16 81908423 missense variant C/G;T snv 5.2E-03 6
rs104893936 0.851 0.120 5 176626472 missense variant C/G;T snv 5.6E-05 4
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
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs104893875 0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs75822236
GBA
0.752 0.200 1 155235002 missense variant C/T snv 1.8E-04 6.1E-05 10
rs78973108
GBA
0.776 0.160 1 155237453 missense variant C/T snv 2.8E-05 4.2E-05 8
rs377591051 0.851 0.080 6 162262651 missense variant C/T snv 4.0E-06 7.0E-06 4
rs113388242 0.925 0.080 3 184327376 missense variant C/T snv 4.0E-05 7.0E-05 3
rs1041833271
APP
0.925 0.080 21 25975995 missense variant C/T snv 7.0E-06 2
rs1342971994 1.000 0.080 4 89822344 missense variant C/T snv 1.4E-05 1