Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs1085307993 0.716 0.440 5 161331056 missense variant C/T snv 53
rs1057519389 0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs61755320 0.716 0.520 16 89546737 missense variant C/T snv 2.9E-03 3.5E-03 41
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs421016
GBA
0.683 0.440 1 155235252 missense variant A/C;G snv 8.0E-06; 1.3E-03 30
rs201893408 0.695 0.480 8 93795970 missense variant T/A;C snv 8.0E-06; 1.5E-04 28
rs1554389088 0.807 0.160 7 44243526 missense variant G/A snv 27
rs6471 0.683 0.360 6 32040110 missense variant G/A;C;T snv 1.2E-05; 5.3E-03 24
rs28936415 0.752 0.320 16 8811153 missense variant G/A snv 4.1E-03 3.7E-03 22
rs104893878 0.732 0.160 4 89835580 missense variant C/G snv 21
rs138659167 0.807 0.320 11 71435840 splice acceptor variant C/A;G snv 5.6E-05; 3.9E-03 20
rs11558538 0.695 0.400 2 138002079 missense variant C/T snv 1.0E-01 8.4E-02 19
rs61750240 0.752 0.240 X 154031020 stop gained G/A;C snv 5.5E-06 19
rs606231435 0.827 0.240 19 41970539 missense variant C/T snv 18
rs387906702 0.807 0.200 X 53403635 missense variant A/G snv 16
rs34778348 0.742 0.120 12 40363526 missense variant G/A snv 1.7E-03 5.8E-04 15
rs1064797245 0.776 0.280 19 41970540 missense variant G/A snv 12
rs104894094 0.763 0.200 9 21971058 missense variant C/A;G;T snv 8.5E-06; 4.3E-06 12
rs1554504663 0.851 0.080 8 23007627 missense variant G/A snv 11
rs1135402761 0.827 0.320 12 79448958 missense variant T/C snv 11
rs775104326 0.776 0.160 3 41224995 stop gained C/A;T snv 4.0E-06 10
rs104893915 0.776 0.200 5 149980428 missense variant C/T snv 9.8E-04 1.0E-03 10
rs768823392 0.827 0.120 16 89546657 coding sequence variant GGCGGGAGA/- delins 2.6E-04 4.2E-04 10