Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs5848 0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs143624519 0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs76980269 0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 10
rs121909335
VCP
0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 9
rs750444386 0.807 0.360 12 117268082 synonymous variant C/A;T snv 4.0E-06; 5.6E-05 6
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
rs2234253 0.827 0.120 6 41161367 missense variant G/A;C;T snv 1.9E-04; 1.0E-02 5
rs763841075
GRN
0.851 0.120 17 44350293 missense variant T/C snv 1.8E-04 1.1E-04 4
rs747019990 0.851 0.120 20 4699336 missense variant C/T snv 3.6E-05 7.0E-06 4
rs63751180
GRN
0.882 0.120 17 44352087 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 3
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