Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs1475170339
IGFALS ; SPSB3
0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs2695121
NR1H2
0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv 15
rs74315452
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 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
SOD1
0.742 0.160 21 31663829 missense variant G/A;C snv 11
rs267606673
ATP7A ; PGK1
0.776 0.240 X 78029314 missense variant C/T snv 9
rs3849942
C9orf72 ; LOC107987057
0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 9
rs387906709
UBQLN2
0.776 0.120 X 56565363 missense variant C/A;T snv 9
rs121912436
SOD1
0.827 0.080 21 31667274 missense variant G/A;C snv 7
rs35801418
LRRK2
0.827 0.120 12 40321114 missense variant A/G snv 7
rs80356733
TARDBP
0.790 0.200 1 11022451 missense variant G/T snv 7
rs3794087
SLC1A2
0.851 0.120 11 35308068 intron variant G/T snv 0.20 6
rs4987023
SOD2
0.807 0.120 6 159692661 missense variant C/T snv 7.0E-06 6
rs63750730
PSEN1
0.827 0.120 14 73173574 missense variant C/T snv 6
rs9268856
HLA-DRB9
0.807 0.240 6 32461942 intron variant C/A;T snv 6
rs121909539
ANG ; RNASE4
0.827 0.120 14 20693753 missense variant C/G snv 5
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