Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7148498 0.851 0.080 14 95641618 intron variant C/T snv 0.12 4
rs730547
LOC105371742
0.851 0.080 17 34785087 intergenic variant C/T snv 0.20 4
rs11061269
ADGRD1
0.851 0.080 12 130971904 intron variant G/A snv 7.5E-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
rs2685056
LOC107986108
0.851 0.080 3 104699729 intergenic variant G/A snv 0.50 4
rs75285952 0.851 0.080 4 27902934 intergenic variant G/A snv 3.3E-02 4
rs9327881 0.851 0.080 5 103389394 intergenic variant G/A snv 0.13 4
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs35714695
SARM1
0.827 0.080 17 28392769 intron variant G/A;T snv 0.12 5
rs7601234
HOXD10
0.851 0.080 2 176116615 5 prime UTR variant G/A;T snv 4
rs969599
PSD3
0.851 0.080 8 18567221 intron variant G/A;T snv 4
rs7117082
OPCML
0.851 0.080 11 133522399 intron variant G/T snv 0.22 4
rs7830371
CLVS1
0.851 0.080 8 61143108 intron variant G/T snv 0.46 4
rs139550538
IDE
0.827 0.080 10 92524312 intron variant T/A snv 1.9E-02 5
rs3849942
C9orf72 ; LOC107987057
0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 9
rs17162257 0.851 0.080 1 26602511 upstream gene variant T/A;G snv 4
rs4761659
LOC643339
0.851 0.080 12 93293308 regulatory region variant T/C snv 0.89 4
rs74315452
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 12
rs16938145 0.851 0.080 9 2256092 intergenic variant T/C;G snv 4
rs1002442
ANK3
0.851 0.080 10 60043304 non coding transcript exon variant T/G snv 0.14 4
rs1559473 0.851 0.080 2 222016799 intergenic variant T/G snv 0.25 4
rs16975050 0.851 0.080 18 41607206 intron variant T/G snv 7.0E-02 4
rs2412208
CAMTA1
0.827 0.080 1 7032722 intron variant T/G snv 0.33 5