Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs74315452
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 12
rs121912431
SOD1
0.742 0.160 21 31663829 missense variant G/A;C snv 11
rs3849942
C9orf72 ; LOC107987057
0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 9
rs121912436
SOD1
0.827 0.080 21 31667274 missense variant G/A;C snv 7
rs121912456
SOD1 ; LOC102724449
0.851 0.120 21 31659806 missense variant G/C snv 6
rs4987023
SOD2
0.807 0.120 6 159692661 missense variant C/T snv 7.0E-06 6
rs121909342
DCTN1
0.827 0.200 2 74378104 missense variant C/G;T 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
rs34517613
KRT18P55
0.827 0.080 17 28283226 intron variant C/T snv 9.1E-02 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
rs616147
MOBP
0.827 0.080 3 39492990 intron variant A/G snv 0.76 5
rs1002442
ANK3
0.851 0.080 10 60043304 non coding transcript exon variant T/G snv 0.14 4
rs10029851 0.851 0.080 4 108706869 intergenic variant A/C;T snv 4
rs10145110
MEG8
0.851 0.080 14 101008533 intron variant C/T snv 9.7E-02 4
rs11061269
ADGRD1
0.851 0.080 12 130971904 intron variant G/A snv 7.5E-02 4
rs115134572
SLC9A9
0.851 0.080 3 143629403 intron variant A/G snv 2.0E-02 4
rs11590421
LOC105378658
0.851 0.080 1 38528443 intergenic variant G/A snv 0.15 4
rs11744876
CTNND2
0.851 0.080 5 11084600 intron variant G/A snv 7.8E-02 4
rs11987758
LOC105377781
0.851 0.080 8 2180583 regulatory region variant G/A snv 0.12 4