Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs74315431
VAPB
0.732 0.080 20 58418318 missense variant C/T snv 4.0E-06 15
rs121912436
SOD1
0.827 0.080 21 31667274 missense variant G/A;C snv 7
rs762060740
GFAP
0.827 0.080 17 44915083 missense variant G/C snv 4.0E-06 6
rs121912437
SOD1
0.851 0.080 21 31667298 missense variant G/A;C;T snv 5
rs12608932
UNC13A
0.827 0.080 19 17641880 intron variant A/C snv 0.36 5
rs139550538
IDE
0.827 0.080 10 92524312 intron variant T/A snv 1.9E-02 5
rs2412208
CAMTA1
0.827 0.080 1 7032722 intron variant T/G snv 0.33 5
rs35714695
SARM1
0.827 0.080 17 28392769 intron variant G/A;T snv 0.12 5
rs3849943
C9orf72 ; LOC107987057
0.827 0.080 9 27543384 non coding transcript exon variant C/G;T snv 5
rs387907264
PFN1
0.851 0.080 17 4946742 missense variant A/C snv 5
rs616147
MOBP
0.827 0.080 3 39492990 intron variant A/G snv 0.76 5
rs774994509
SOD1
0.851 0.080 21 31667296 missense variant A/G snv 4.0E-06 5
rs886041390
FUS
0.827 0.080 16 31191431 missense variant C/T snv 4.0E-06 5
rs1159805691
SPSB3 ; IGFALS
0.851 0.080 16 1792266 frameshift variant T/- del 7.0E-06 4
rs121912439
SOD1
0.851 0.080 21 31667320 missense variant A/G snv 4
rs1239669755
IQCG ; LMLN
0.851 0.080 3 197960384 missense variant C/T snv 4
rs2736990
SNCA
0.882 0.080 4 89757390 intron variant G/A;T snv 4
rs730880030
CHCHD10 ; LOC107985577
0.851 0.080 22 23767591 missense variant C/A snv 4
rs12136973
KIAA0040
1.000 0.080 1 175171183 intron variant T/C snv 0.22 3
rs121912440
SOD1
0.882 0.080 21 31667337 missense variant C/G;T snv 3
rs121912455
SOD1
0.882 0.080 21 31666496 missense variant G/A;T snv 4.0E-06 3
rs1226494987
MATR3
0.882 0.080 5 139317091 missense variant C/G snv 4.0E-06 3
rs1424014997
SCAF4 ; SOD1
0.882 0.080 21 31668562 missense variant T/C snv 8.0E-06 3
rs148156462
COQ2
0.925 0.080 4 83264287 missense variant A/G snv 4.2E-03 1.6E-03 3
rs1541160
KIFAP3
0.882 0.080 1 170026661 intron variant C/A;T snv 3