Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9977018 0.851 0.080 21 41616809 intergenic variant T/G snv 0.24 4
rs9825420
ITGA9
0.851 0.080 3 37562521 intron variant T/G snv 0.18 4
rs969599
PSD3
0.851 0.080 8 18567221 intron variant G/A;T snv 4
rs9568797
OLFM4
0.851 0.080 13 53039424 intron variant C/G;T snv 4
rs9329300 0.851 0.080 10 2747402 intergenic variant A/C;G snv 4
rs9327881 0.851 0.080 5 103389394 intergenic variant G/A snv 0.13 4
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03 16
rs7999075 0.851 0.080 13 22046068 intron variant C/A snv 0.88 4
rs7830371
CLVS1
0.851 0.080 8 61143108 intron variant G/T snv 0.46 4
rs7601234
HOXD10
0.851 0.080 2 176116615 5 prime UTR variant G/A;T snv 4
rs75285952 0.851 0.080 4 27902934 intergenic variant G/A snv 3.3E-02 4
rs730547
LOC105371742
0.851 0.080 17 34785087 intergenic variant C/T snv 0.20 4
rs72911847 0.851 0.080 2 193714051 intergenic variant A/G snv 3.3E-02 4
rs7148498 0.851 0.080 14 95641618 intron variant C/T snv 0.12 4
rs7117082
OPCML
0.851 0.080 11 133522399 intron variant G/T snv 0.22 4
rs616147
MOBP
0.827 0.080 3 39492990 intron variant A/G snv 0.76 5
rs6137726 0.851 0.080 20 22691782 intron variant C/A snv 0.25 4
rs551585 0.851 0.080 1 76660688 intergenic variant C/A snv 8.9E-02 4
rs4761659
LOC643339
0.851 0.080 12 93293308 regulatory region variant T/C snv 0.89 4
rs4482178
LINC00351
0.851 0.080 13 85529954 intron variant C/A snv 8.4E-02 4
rs4424056 0.851 0.080 6 91135689 intergenic variant T/G snv 0.76 4
rs4234080
METTL21A
0.851 0.080 2 207624377 5 prime UTR variant C/A snv 0.19 0.23 4
rs4148112
ABCG1
0.851 0.080 21 42230666 intron variant C/T snv 1.8E-03 4
rs3852053
MASP1
0.851 0.080 3 187219412 3 prime UTR variant T/G snv 0.47 4
rs3849943
C9orf72 ; LOC107987057
0.827 0.080 9 27543384 non coding transcript exon variant C/G;T snv 5