Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs1475170339
IGFALS ; SPSB3
0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03 16
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv 15
rs74315431
VAPB
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
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 12
rs80356726
TARDBP
0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 12
rs121912431
SOD1
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
rs387906709
UBQLN2
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
rs745805222
IGF1
0.790 0.120 12 102475722 synonymous variant C/T snv 1.2E-05 4.9E-05 7
rs62643364
PRNP
0.851 0.160 20 4699466 synonymous variant A/G;T snv 4.0E-06; 1.4E-04 7
rs121912433
SOD1
0.827 0.120 21 31663841 missense variant G/A snv 4.0E-06 7
rs121912436
SOD1
0.827 0.080 21 31667274 missense variant G/A;C snv 7
rs121912442
SOD1 ; LOC102724449
0.807 0.120 21 31659783 missense variant C/T snv 3.6E-05 7
rs80356730
TARDBP
0.807 0.120 1 11022418 missense variant A/G snv 8.0E-06 7
rs80356733
TARDBP
0.790 0.200 1 11022451 missense variant G/T snv 7
rs762060740
GFAP
0.827 0.080 17 44915083 missense variant G/C snv 4.0E-06 6
rs121912452
SOD1
0.807 0.120 21 31667271 missense variant T/C;G snv 4.0E-06 6
rs4987023
SOD2
0.807 0.120 6 159692661 missense variant C/T snv 7.0E-06 6
rs387906711
UBQLN2
0.807 0.120 X 56565389 missense variant C/A;T snv 6.6E-06 6