Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10029851 0.851 0.080 4 108706869 intergenic variant A/C;T snv 4
rs121909668
FUS
0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 8
rs1464443
ERBB4
0.851 0.080 2 212050001 intron variant C/A;T snv 4
rs16938145 0.851 0.080 9 2256092 intergenic variant T/C;G snv 4
rs17162257 0.851 0.080 1 26602511 upstream gene variant T/A;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
rs7601234
HOXD10
0.851 0.080 2 176116615 5 prime UTR variant G/A;T snv 4
rs886041390
FUS
0.827 0.080 16 31191431 missense variant C/T snv 4.0E-06 5
rs9329300 0.851 0.080 10 2747402 intergenic variant A/C;G snv 4
rs9568797
OLFM4
0.851 0.080 13 53039424 intron variant C/G;T snv 4
rs969599
PSD3
0.851 0.080 8 18567221 intron variant G/A;T snv 4
rs4148112
ABCG1
0.851 0.080 21 42230666 intron variant C/T snv 1.8E-03 4
rs139550538
IDE
0.827 0.080 10 92524312 intron variant T/A snv 1.9E-02 5
rs115134572
SLC9A9
0.851 0.080 3 143629403 intron variant A/G snv 2.0E-02 4
rs72911847 0.851 0.080 2 193714051 intergenic variant A/G snv 3.3E-02 4
rs75285952 0.851 0.080 4 27902934 intergenic variant G/A snv 3.3E-02 4
rs16975050 0.851 0.080 18 41607206 intron variant T/G snv 7.0E-02 4
rs11061269
ADGRD1
0.851 0.080 12 130971904 intron variant G/A snv 7.5E-02 4
rs11744876
CTNND2
0.851 0.080 5 11084600 intron variant G/A snv 7.8E-02 4
rs4482178
LINC00351
0.851 0.080 13 85529954 intron variant C/A snv 8.4E-02 4
rs551585 0.851 0.080 1 76660688 intergenic variant C/A snv 8.9E-02 4
rs34517613
KRT18P55
0.827 0.080 17 28283226 intron variant C/T snv 9.1E-02 5
rs10145110
MEG8
0.851 0.080 14 101008533 intron variant C/T snv 9.7E-02 4
rs7148498 0.851 0.080 14 95641618 intron variant C/T snv 0.12 4