Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4859147 1.000 0.120 3 182964065 intron variant T/C snv 0.56 0.48 1
rs1052352
FUS
0.925 0.120 16 31183958 synonymous variant C/T snv 0.53 0.45 2
rs3173615 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs10814083 0.882 0.160 9 34256349 synonymous variant C/T snv 0.40 0.34 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
rs1133763 0.882 0.200 17 34320812 missense variant A/C snv 0.21 0.15 4
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs17350674 1.000 0.120 9 34306412 stop gained C/A;T snv 0.16; 4.1E-06 1
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs2234253 0.827 0.120 6 41161367 missense variant G/A;C;T snv 1.9E-04; 1.0E-02 5
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs143624519 0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs63750541
GRN
0.851 0.160 17 44351586 missense variant G/A;C snv 8.4E-04 4
rs63750096 1.000 0.120 17 45996557 missense variant G/A;T snv 6.3E-04 1
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs763841075
GRN
0.851 0.120 17 44350293 missense variant T/C snv 1.8E-04 1.1E-04 4
rs750444386 0.807 0.360 12 117268082 synonymous variant C/A;T snv 4.0E-06; 5.6E-05 6
rs750810467
GRN
1.000 0.120 17 44351420 missense variant G/A;C snv 4.8E-05; 4.0E-06 1
rs747019990 0.851 0.120 20 4699336 missense variant C/T snv 3.6E-05 7.0E-06 4
rs76980269 0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 10
rs63750756 0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs753009660 1.000 0.120 X 56564910 missense variant C/G snv 2.2E-05 3.8E-05 1
rs533451404
GRN
0.925 0.120 17 44349267 missense variant G/A snv 1.6E-05 2.1E-05 2