Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1464443
ERBB4
0.851 0.080 2 212050001 intron variant C/A;T snv 4
rs2457174
FSTL4
0.851 0.080 5 133843389 intergenic variant C/T snv 0.33 4
rs7601234
HOXD10
0.851 0.080 2 176116615 5 prime UTR variant G/A;T snv 4
rs139550538
IDE
0.827 0.080 10 92524312 intron variant T/A snv 1.9E-02 5
rs2667100
INPP4B
0.851 0.080 4 142054920 intron variant A/G snv 0.81 4
rs9825420
ITGA9
0.851 0.080 3 37562521 intron variant T/G snv 0.18 4
rs13100616
KCNMB2-AS1 ; KCNMB2
0.851 0.080 3 178681763 intron variant A/G snv 0.33 4
rs34517613
KRT18P55
0.827 0.080 17 28283226 intron variant C/T snv 9.1E-02 5
rs4482178
LINC00351
0.851 0.080 13 85529954 intron variant C/A snv 8.4E-02 4
rs730547
LOC105371742
0.851 0.080 17 34785087 intergenic variant C/T snv 0.20 4
rs11987758
LOC105377781
0.851 0.080 8 2180583 regulatory region variant G/A snv 0.12 4
rs11590421
LOC105378658
0.851 0.080 1 38528443 intergenic variant G/A snv 0.15 4
rs2685056
LOC107986108
0.851 0.080 3 104699729 intergenic variant G/A snv 0.50 4
rs4761659
LOC643339
0.851 0.080 12 93293308 regulatory region variant T/C snv 0.89 4
rs3852053
MASP1
0.851 0.080 3 187219412 3 prime UTR variant T/G snv 0.47 4
rs10145110
MEG8
0.851 0.080 14 101008533 intron variant C/T snv 9.7E-02 4
rs4234080
METTL21A
0.851 0.080 2 207624377 5 prime UTR variant C/A snv 0.19 0.23 4
rs616147
MOBP
0.827 0.080 3 39492990 intron variant A/G snv 0.76 5
rs9568797
OLFM4
0.851 0.080 13 53039424 intron variant C/G;T snv 4
rs7117082
OPCML
0.851 0.080 11 133522399 intron variant G/T snv 0.22 4
rs969599
PSD3
0.851 0.080 8 18567221 intron variant G/A;T snv 4
rs35714695
SARM1
0.827 0.080 17 28392769 intron variant G/A;T snv 0.12 5
rs1400816
SLC25A12
0.851 0.080 2 171824168 intron variant A/C snv 0.81 4
rs115134572
SLC9A9
0.851 0.080 3 143629403 intron variant A/G snv 2.0E-02 4
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58