Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17162257 0.851 0.080 1 26602511 upstream gene variant T/A;G snv 4
rs9329300 0.851 0.080 10 2747402 intergenic variant A/C;G snv 4
rs3849942
C9orf72 ; LOC107987057
0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 9
rs3849943
C9orf72 ; LOC107987057
0.827 0.080 9 27543384 non coding transcript exon variant C/G;T snv 5
rs75285952 0.851 0.080 4 27902934 intergenic variant G/A snv 3.3E-02 4
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
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03 16
rs121912438
SOD1
0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs74315452
SOD1
0.732 0.160 21 31667356 missense variant T/C snv 12
rs730547
LOC105371742
0.851 0.080 17 34785087 intergenic variant C/T snv 0.20 4
rs9825420
ITGA9
0.851 0.080 3 37562521 intron variant T/G snv 0.18 4
rs11590421
LOC105378658
0.851 0.080 1 38528443 intergenic variant G/A snv 0.15 4
rs616147
MOBP
0.827 0.080 3 39492990 intron variant A/G snv 0.76 5
rs16975050 0.851 0.080 18 41607206 intron variant T/G snv 7.0E-02 4
rs9977018 0.851 0.080 21 41616809 intergenic variant T/G snv 0.24 4
rs4148112
ABCG1
0.851 0.080 21 42230666 intron variant C/T snv 1.8E-03 4
rs1605070 0.851 0.080 3 51882999 intergenic variant C/A snv 0.60 4
rs9568797
OLFM4
0.851 0.080 13 53039424 intron variant C/G;T snv 4
rs1002442
ANK3
0.851 0.080 10 60043304 non coding transcript exon variant T/G snv 0.14 4
rs7830371
CLVS1
0.851 0.080 8 61143108 intron variant G/T snv 0.46 4
rs12891047
ZFYVE26
0.851 0.080 14 67776358 intron variant C/A snv 0.62 4
rs2412208
CAMTA1
0.827 0.080 1 7032722 intron variant T/G snv 0.33 5
rs551585 0.851 0.080 1 76660688 intergenic variant C/A snv 8.9E-02 4
rs4482178
LINC00351
0.851 0.080 13 85529954 intron variant C/A snv 8.4E-02 4