Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs1475170339
IGFALS ; SPSB3
0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv 15
rs121912431
SOD1
0.742 0.160 21 31663829 missense variant G/A;C snv 11
rs80356733
TARDBP
0.790 0.200 1 11022451 missense variant G/T snv 7
rs121909671
FUS
0.851 0.120 16 31191419 missense variant G/A;T snv 4.0E-06 6
rs762060740
GFAP
0.827 0.080 17 44915083 missense variant G/C snv 4.0E-06 6
rs121909342
DCTN1
0.827 0.200 2 74378104 missense variant C/G;T snv 5
rs387907264
PFN1
0.851 0.080 17 4946742 missense variant A/C snv 5
rs763459583
MAPT
0.882 0.080 17 45987045 missense variant A/G;T snv 4.0E-06; 4.0E-06 3
rs781978795
CALCA ; CALCB
0.925 0.080 11 14968884 missense variant C/G snv 2.0E-05 2
rs1171108843
CDCA5
0.925 0.040 11 65079421 stop lost T/C snv 2
rs1355231200
CHGA
0.925 0.080 14 92931340 frameshift variant C/- delins 2
rs1426039367
CSF2
0.925 0.080 5 132073916 synonymous variant G/A snv 7.0E-06 2
rs199714029
FCN2
0.925 0.040 9 134886483 missense variant G/A snv 2
rs1365988292
ITGAM
0.925 0.080 16 31261756 synonymous variant A/G snv 2
rs1279258206
USP2-AS1 ; THY1
0.925 0.080 11 119420222 missense variant C/T snv 4.0E-06 2
rs1394871648
ALS2
1.000 2 201761816 missense variant C/T snv 4.1E-06 1
rs1284398161
MAP2K1
1.000 15 66485125 missense variant T/A snv 1
rs141818899
PCBP1-AS1 ; PCBP1
1.000 2 70087836 synonymous variant G/A snv 4.0E-06 7.0E-06 1
rs759299980
SORBS1
1.000 10 95341599 missense variant C/T snv 8.0E-06 7.0E-06 1