Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2275235
CTSS
1.000 0.120 1 150757803 intron variant A/G snv 0.34 1
rs774320676
CTSS
1.000 0.120 1 150750091 missense variant A/T snv 4.0E-06 1
rs928508030
CTSS
1.000 0.120 1 150765698 splice region variant G/A snv 1
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs55951658
CYP3A4
0.827 0.200 7 99770202 missense variant T/A;C snv 4.1E-04 9.8E-05 7
rs9333025
CYP4A11
0.851 0.200 1 46931231 intron variant C/T snv 9.4E-02 8
rs2108622
CYP4F2
0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 20
rs1207570776
DNAJC10
1.000 0.120 2 182757711 missense variant A/G snv 1
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs3789683
F3
0.925 0.200 1 94530506 missense variant C/T snv 6.5E-03 1.0E-02 3
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs1801273
FABP1
0.925 0.200 2 88126256 missense variant C/T snv 1.2E-05 2.1E-05 3
rs1799883
FABP2
0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs4806942
GIPC3
1.000 0.120 19 3589341 intron variant G/A snv 0.13 1
rs2249825
HMGB1
0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs11614913
HOXC6 ; MIR196A2
0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs2162679
IGF1
0.851 0.240 12 102477481 intron variant C/G;T snv 6
rs7956547
IGF1
0.925 0.120 12 102465038 intron variant T/C snv 0.25 2
rs2072592
IGF1 ; LINC02456
0.925 0.120 12 102419854 intron variant C/T snv 2.8E-02 2
rs978458
IGF1 ; LINC02456
0.925 0.120 12 102408461 intron variant T/C snv 0.69 2
rs1800896
IL19 ; IL10
0.507 0.800 1 206773552 intron variant T/C snv 0.41 113