Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1133763 0.882 0.200 17 34320812 missense variant A/C snv 0.21 0.15 4
rs63750129 0.882 0.120 17 45996612 missense variant A/C snv 4.0E-06 4
rs1390191775 1.000 0.120 X 56564879 missense variant A/C;G snv 5.5E-06; 5.5E-06 1
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs4795541 0.807 0.200 17 30237299 upstream gene variant A/G snv 7
rs267607102 0.851 0.120 1 11022196 missense variant A/G snv 5
rs80356717 0.851 0.120 1 11018836 missense variant A/G snv 5
rs752076094
FUS
0.925 0.120 16 31185175 missense variant A/G snv 8.4E-06 2.8E-05 2
rs63750092 0.882 0.120 17 46014277 missense variant A/T snv 3
rs3173615 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs63751180
GRN
0.882 0.120 17 44352087 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 3
rs741810
FUS
0.925 0.120 16 31182621 synonymous variant C/A;G;T snv 0.32; 4.0E-06; 4.0E-06 2
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs750444386 0.807 0.360 12 117268082 synonymous variant C/A;T snv 4.0E-06; 5.6E-05 6
rs63751243
GRN
0.882 0.160 17 44349190 missense variant C/A;T snv 4.0E-06 4
rs17350674 1.000 0.120 9 34306412 stop gained C/A;T snv 0.16; 4.1E-06 1
rs1417841099 1.000 0.120 19 852917 missense variant C/G snv 4.6E-06 1
rs753009660 1.000 0.120 X 56564910 missense variant C/G snv 2.2E-05 3.8E-05 1
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs63750349 0.851 0.200 17 45996638 missense variant C/G;T snv 4.0E-06 5
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
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs63750424 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30