Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs1481950 1.000 0.080 8 53777725 intron variant C/A;G snv 2
rs766001707 0.851 0.200 14 92096772 missense variant C/T snv 6
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs755221106 0.851 0.040 17 50617560 missense variant G/A;T snv 4.0E-06 7
rs1424266770 0.790 0.200 4 184632307 missense variant C/G snv 8.0E-06 10
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs104894201 0.763 0.280 11 111908934 missense variant T/C snv 12
rs371557337 1.000 0.040 5 150733475 start lost T/C;G snv 7.0E-06 2
rs387907043 0.925 0.120 20 63930873 missense variant T/A;G snv 4.0E-06 3
rs5848 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs75548401
GBA
0.882 0.160 1 155236246 missense variant G/A snv 5.9E-03 6.2E-03 6
rs63751294
GRN
0.827 0.120 17 44352404 stop gained C/T snv 8.0E-06 6
rs63751177
GRN
1.000 0.120 17 44351438 stop gained G/A snv 2
rs121909715
GSN
0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 8
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs156697 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs587777606 0.851 0.160 11 62691300 stop gained G/A snv 4.0E-06 7.0E-06 6
rs66468541 0.925 0.080 2 197497275 missense variant C/T snv 4
rs1264519280 1.000 0.040 1 32014083 missense variant G/A snv 2
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262