Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3849942
C9orf72 ; LOC107987057
0.776 0.200 9 27543283 non coding transcript exon variant T/A;C snv 9
rs121909668
FUS
0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 8
rs121909671
FUS
0.851 0.120 16 31191419 missense variant G/A;T snv 4.0E-06 6
rs3849943
C9orf72 ; LOC107987057
0.827 0.080 9 27543384 non coding transcript exon variant C/G;T snv 5
rs2412208
CAMTA1
0.827 0.080 1 7032722 intron variant T/G snv 0.33 5
rs886041390
FUS
0.827 0.080 16 31191431 missense variant C/T snv 4.0E-06 5
rs139550538
IDE
0.827 0.080 10 92524312 intron variant T/A snv 1.9E-02 5
rs34517613
KRT18P55
0.827 0.080 17 28283226 intron variant C/T snv 9.1E-02 5
rs616147
MOBP
0.827 0.080 3 39492990 intron variant A/G snv 0.76 5
rs35714695
SARM1
0.827 0.080 17 28392769 intron variant G/A;T snv 0.12 5
rs12608932
UNC13A
0.827 0.080 19 17641880 intron variant A/C snv 0.36 5
rs10029851 0.851 0.080 4 108706869 intergenic variant A/C;T snv 4
rs1559473 0.851 0.080 2 222016799 intergenic variant T/G snv 0.25 4
rs1605070 0.851 0.080 3 51882999 intergenic variant C/A snv 0.60 4
rs16938145 0.851 0.080 9 2256092 intergenic variant T/C;G snv 4
rs16975050 0.851 0.080 18 41607206 intron variant T/G snv 7.0E-02 4
rs17162257 0.851 0.080 1 26602511 upstream gene variant T/A;G snv 4
rs2322978 0.851 0.080 11 127846245 intergenic variant A/G snv 0.74 4
rs4424056 0.851 0.080 6 91135689 intergenic variant T/G snv 0.76 4
rs551585 0.851 0.080 1 76660688 intergenic variant C/A snv 8.9E-02 4
rs6137726 0.851 0.080 20 22691782 intron variant C/A snv 0.25 4
rs7148498 0.851 0.080 14 95641618 intron variant C/T snv 0.12 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
rs7999075 0.851 0.080 13 22046068 intron variant C/A snv 0.88 4