Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1041833271
APP
0.925 0.080 21 25975995 missense variant C/T snv 7.0E-06 2
rs104886460
GBA
0.776 0.160 1 155240629 splice donor variant C/A;T snv 7.6E-05 8
rs104893875 0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs104893878 0.732 0.160 4 89835580 missense variant C/G snv 21
rs104893936 0.851 0.120 5 176626472 missense variant C/G;T snv 5.6E-05 4
rs104893937 0.851 0.120 5 176621218 missense variant G/T snv 1.7E-04 2.0E-04 4
rs1064651
GBA
0.732 0.360 1 155235727 missense variant C/G snv 1.3E-04 2.0E-04 13
rs112176450 0.807 0.080 3 184327401 missense variant G/A;T snv 2.1E-04 2.8E-04 7
rs113388242 0.925 0.080 3 184327376 missense variant C/T snv 4.0E-05 7.0E-05 3
rs12734374 1.000 0.080 1 155419060 intron variant A/T snv 3.4E-02 2
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs1330229174 0.925 0.080 4 89835568 missense variant T/C snv 4.0E-06 2
rs1342971994 1.000 0.080 4 89822344 missense variant C/T snv 1.4E-05 1
rs143624519 0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs1446915570 0.925 0.080 14 73173623 synonymous variant A/T snv 4.0E-06 7.0E-06 2
rs2306604 0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs35749011 0.925 0.080 1 155162560 intergenic variant G/A snv 1.1E-02 2
rs377591051 0.851 0.080 6 162262651 missense variant C/T snv 4.0E-06 7.0E-06 4
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs616338 0.925 0.080 17 49219935 missense variant T/C snv 0.99 0.99 2