Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs75932628 0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs1475170339 0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs121912443 0.732 0.160 21 31663857 missense variant A/G snv 15
rs367543041 0.742 0.200 1 11022553 missense variant G/A;C snv 3.0E-05 15
rs74315431 0.732 0.080 20 58418318 missense variant C/T snv 4.0E-06 15
rs387906789
VCP
0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 14
rs74315452 0.732 0.160 21 31667356 missense variant T/C snv 12
rs80356726 0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12
rs121909329
VCP
0.763 0.200 9 35065363 missense variant C/A;G;T snv 11
rs121909330
VCP
0.752 0.200 9 35065364 missense variant G/A;C;T snv 11
rs121912431 0.742 0.160 21 31663829 missense variant G/A;C snv 11
rs121909334
VCP
0.752 0.200 9 35065255 missense variant C/T snv 1.6E-05 10
rs1424266770 0.790 0.200 4 184632307 missense variant C/G snv 8.0E-06 10
rs121909335
VCP
0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 9
rs267606673 0.776 0.240 X 78029314 missense variant C/T snv 9
rs3849942 0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 9
rs387906709 0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs121909668
FUS
0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 8
rs121912433 0.827 0.120 21 31663841 missense variant G/A snv 4.0E-06 7