Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs80356717 0.851 0.120 1 11018836 missense variant A/G snv 5
rs267607102 0.851 0.120 1 11022196 missense variant A/G snv 5
rs80356726 0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12
rs750444386 0.807 0.360 12 117268082 synonymous variant C/A;T snv 4.0E-06; 5.6E-05 6
rs76980269 0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 10
rs3173615 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1163763 0.925 0.120 12 17567834 intron variant G/T snv 0.24 2
rs4859147 1.000 0.120 3 182964065 intron variant T/C snv 0.56 0.48 1
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
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
rs1431475678 1.000 0.120 11 27658555 missense variant G/C snv 7.0E-06 1
rs1415210991 1.000 0.120 11 27701003 5 prime UTR variant G/C snv 4.2E-06 1
rs4795541 0.807 0.200 17 30237299 upstream gene variant A/G snv 7
rs741810
FUS
0.925 0.120 16 31182621 synonymous variant C/A;G;T snv 0.32; 4.0E-06; 4.0E-06 2
rs1052352
FUS
0.925 0.120 16 31183958 synonymous variant C/T snv 0.53 0.45 2
rs752076094
FUS
0.925 0.120 16 31185175 missense variant A/G snv 8.4E-06 2.8E-05 2
rs1319062081 0.925 0.120 21 31668537 stop gained G/T snv 2
rs706118 1.000 0.120 9 33256181 intron variant T/G snv 0.39 1
rs10814083 0.882 0.160 9 34256349 synonymous variant C/T snv 0.40 0.34 3
rs17350674 1.000 0.120 9 34306412 stop gained C/A;T snv 0.16; 4.1E-06 1
rs1133763 0.882 0.200 17 34320812 missense variant A/C snv 0.21 0.15 4