Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs201106962 0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 5
rs767543900 0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs2306604 0.827 0.080 10 58388932 intron variant A/C;G;T snv 5
rs3764435 0.827 0.120 9 72901960 intron variant A/C;T snv 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2420616 0.882 0.080 10 119316984 intron variant A/G snv 0.69 3
rs334558 0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs33939927 0.708 0.120 12 40310434 missense variant C/A;G;T snv 4.0E-06; 1.2E-05 24
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
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
rs121909334
VCP
0.752 0.200 9 35065255 missense variant C/T snv 1.6E-05 10
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs1801474 0.851 0.080 6 162201165 missense variant C/T snv 7.1E-02 5.3E-02 4
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs2230288
GBA
0.776 0.160 1 155236376 missense variant C/T snv 1.0E-02 1.0E-02 18
rs4752293 0.882 0.080 10 119342186 intron variant C/T snv 0.74 3
rs5848 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
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
rs242557 0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78